Article(id=1193632556458406381, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1193558470239678932, articleNumber=null, orderNo=null, doi=10.16438/j.0513-4870.2024-0698, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=research-article, receivedDate=1721577600000, receivedDateStr=2024-07-22, revisedDate=1725811200000, revisedDateStr=2024-09-09, acceptedDate=null, acceptedDateStr=null, onlineDate=1762513778080, onlineDateStr=2025-11-07, pubDate=1736611200000, pubDateStr=2025-01-12, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1762513778080, onlineIssueDateStr=2025-11-07, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1762513778080, creator=13701087609, updateTime=1762513778080, updator=13701087609, issue=Issue{id=1193558470239678932, tenantId=1146029695717560320, journalId=1189982191388893191, year='2025', volume='60', issue='1', pageStart='1', pageEnd='244', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1762496114549, creator=13701087609, updateTime=1764224942173, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1200809698921402865, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1193558470239678932, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1200809698921402866, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1193558470239678932, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=172, endPage=178, ext={EN=ArticleExt(id=1193632557477622255, articleId=1193632556458406381, tenantId=1146029695717560320, journalId=1189982191388893191, language=EN, title=Synthesis and anti-tumor activity of ursolic acid-triazole derivatives, columnId=1190335348761793317, journalTitle=Acta Pharmaceutica Sinica, columnName=Original Articles, runingTitle=null, highlight=null, articleAbstract=
Ten ursolic acid derivatives were designed from the lead compound ursolic acid by introducing 1, 2, 3-triazole at C-3 and C-28. The target compounds were synthesized and characterized by 1H NMR and 13C NMR. MTT assay was used to study the antitumor activity of these compounds in human cancer cells with high expression (MCF-7 and SGC-7901). The results showed that the antitumor activity of all compounds on MCF-7 and SGC-7901 tumor cells was significantly higher than that of ursolic acid. The compound Ⅱ4 exhibited significant antitumor activity which was equivalent to the positive control drug nilotinib, molecular docking showed that the compound Ⅱ4 have high binding ability with c-Kit, which deserves further research.
, correspAuthors=Zhen-yu KUAI, authorNote=null, correspAuthorsNote=null, copyrightStatement=Copyright ©2025 Acta Pharmaceutica Sinica. All rights reserved., copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=Zhen-yu KUAI, Yan-qiu MENG), CN=ArticleExt(id=1193632810167661499, articleId=1193632556458406381, tenantId=1146029695717560320, journalId=1189982191388893191, language=CN, title=熊果酸-三氮唑衍生物的合成及抗肿瘤活性研究, columnId=1190335348896011050, journalTitle=药学学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=
以熊果酸为母体, 对其C-3和C-28位进行结构修饰, 引入1, 2, 3-三氮唑, 合成了10个新型熊果酸衍生物, 结构经MS、1H NMR和13C NMR确证。通过MTT法, 选用高表达人癌细胞(乳腺癌MCF-7和胃癌SGC-7901细胞) 对化合物进行初步体外抗肿瘤活性筛选, 结果表明, 所有化合物对MCF-7和SGC-7901肿瘤细胞的抑制活性均明显高于熊果酸。其中化合物Ⅱ4对MCF-7和SGC-7901细胞具有较强的抗肿瘤作用, 活性与阳性对照药尼洛替尼相当, 分子对接也显示其与c-Kit具有较高的结合能力, 值得进一步研究。
, correspAuthors=蒯振彧, authorNote=null, correspAuthorsNote=
, copyrightStatement=版权所有©《药学学报》编辑部2025, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=ms4kjFCAewDcbqvI7puEpA==, magXml=Lt+kA65zf1UfQ06JT2rE0Q==, pdfUrl=null, pdf=SHNcrVamB+j6eJDIaDao3Q==, pdfFileSize=2052773, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=AkF08I7nZvdijl6NuZa3IQ==, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=h/1/FAF4C/bSzqyM7f14Aw==, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=蒯振彧, 孟艳秋)}, authors=[Author(id=1194708176172978868, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=zhenyukuai999@163.com, emailSecond=null, emailThird=null, correspondingAuthor=1, authorType=1, ext={EN=AuthorExt(id=1194708176261059254, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, authorId=1194708176172978868, language=EN, stringName=Zhen-yu KUAI, firstName=Zhen-yu, middleName=null, lastName=KUAI, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
1, *, address=1. Department of Pharmacy Teaching and Research, Maanshan Technical College, Maanshan 243031, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1194708176349139639, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, authorId=1194708176172978868, language=CN, stringName=蒯振彧, firstName=振彧, middleName=null, lastName=蒯, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
1, *, address=1.马鞍山职业技术学院药学教研室, 安徽 马鞍山 243031, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1194708175967457965, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, xref=null, ext=[AuthorCompanyExt(id=1194708175975846574, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708175967457965, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1. Department of Pharmacy Teaching and Research, Maanshan Technical College, Maanshan 243031, China), AuthorCompanyExt(id=1194708175984235183, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708175967457965, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.马鞍山职业技术学院药学教研室, 安徽 马鞍山 243031)])]), Author(id=1194708176403665593, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, orderNo=1, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1194708176474968763, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, authorId=1194708176403665593, language=EN, stringName=Yan-qiu MENG, firstName=Yan-qiu, middleName=null, lastName=MENG, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
2, address=2. Department of Pharmaceutical Engineering, Shenyang University of Chemical Technology, Shenyang 110142, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1194708176558854844, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, authorId=1194708176403665593, language=CN, stringName=孟艳秋, firstName=艳秋, middleName=null, lastName=孟, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
2, address=2.沈阳化工大学制药与生物工程学院, 辽宁 沈阳 110142, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1194708176038761136, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, xref=null, ext=[AuthorCompanyExt(id=1194708176047149745, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708176038761136, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2. Department of Pharmaceutical Engineering, Shenyang University of Chemical Technology, Shenyang 110142, China), AuthorCompanyExt(id=1194708176051344050, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708176038761136, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.沈阳化工大学制药与生物工程学院, 辽宁 沈阳 110142)])])], keywords=[Keyword(id=1194708176688878269, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, orderNo=1, keyword=ursolic acid), Keyword(id=1194708176789541566, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, orderNo=2, keyword=molecular docking), Keyword(id=1194708176890204863, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, orderNo=3, keyword=c-Kit), Keyword(id=1194708177167028928, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, orderNo=4, keyword=structural modification), Keyword(id=1194708177359966913, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, orderNo=5, keyword=anti-tumor activity), Keyword(id=1194708177510961858, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, orderNo=1, keyword=熊果酸), Keyword(id=1194708177594847939, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, orderNo=2, keyword=分子对接), Keyword(id=1194708177712288452, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, orderNo=3, keyword=c-Kit), Keyword(id=1194708177821340357, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, orderNo=4, keyword=结构修饰), Keyword(id=1194708177938780870, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, orderNo=5, keyword=抗肿瘤活性)], refs=[Reference(id=1194708182602846948, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[1], rfOrder=0, authorNames=null, journalName=null, refType=null, unstructuredReference=Mlala S, Oyedeji AO, Gondwe M, et al. Molecules ursolic acid and its derivatives as bioactive agents [J]. Molecules, 2019, 24: 2751., articleTitle=null, refAbstract=null), Reference(id=1194708182682538727, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[2], rfOrder=1, authorNames=null, journalName=null, refType=null, unstructuredReference=Cargnin ST, Gnoatto SB. Ursolic acid from apple pomace and traditional plants: a valuable triterpenoid with functional properties [J]. Food Chem, 2017, 220: 477-489., articleTitle=null, refAbstract=null), Reference(id=1194708182770619113, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[3], rfOrder=2, authorNames=null, journalName=null, refType=null, unstructuredReference=Liu ZY, Huang HL, Yu Y, et al. Exploring the potential mechanism of action of ursolic acid against gastric cancer and COVID-19 using network pharmacology and bioinformatics analysis [J]. Curr Pharm Des, 2023, 29: 1274-1292., articleTitle=null, refAbstract=null), Reference(id=1194708182841922283, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[4], rfOrder=3, authorNames=null, journalName=null, refType=null, unstructuredReference=Wang WJ, Liu CC, Li YT, et al. Antifungal and antibiofilm
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The development of imatinib that opened up new fields of molecular targeted drugs and anti-resistant nilotinib [J]. Acta Pharm Sin (药学学报), 2019, 54: 753-759., articleTitle=null, refAbstract=null), Reference(id=1194708184448340760, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[23], rfOrder=22, authorNames=null, journalName=null, refType=null, unstructuredReference=Meng YQ, Zhao YW, Kuai ZY, et al. Synthesis and antitumor activity evaluation of novel oleanolic acid derivatives [J]. J Asian Nat Prod Res, 2017, 19: 1000-1010., articleTitle=null, refAbstract=null)], funds=[Fund(id=1194708182057587419, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, awardId=2024AH051790, language=CN, fundingSource=安徽省高校自然科学研究项目(2024AH051790), fundOrder=null, country=null), Fund(id=1194708182116307676, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, awardId=KJ2021A1340, language=CN, fundingSource=安徽省高校自然科学研究项目(KJ2021A1340), fundOrder=null, country=null), Fund(id=1194708182191805149, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, awardId=82473787, language=CN, fundingSource=国家自然科学基金资助项目(82473787), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1194708175967457965, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, xref=null, ext=[AuthorCompanyExt(id=1194708175975846574, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708175967457965, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1. Department of Pharmacy Teaching and Research, Maanshan Technical College, Maanshan 243031, China), AuthorCompanyExt(id=1194708175984235183, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708175967457965, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.马鞍山职业技术学院药学教研室, 安徽 马鞍山 243031)]), AuthorCompany(id=1194708176038761136, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, xref=null, ext=[AuthorCompanyExt(id=1194708176047149745, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708176038761136, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2. Department of Pharmaceutical Engineering, Shenyang University of Chemical Technology, Shenyang 110142, China), AuthorCompanyExt(id=1194708176051344050, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, companyId=1194708176038761136, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.沈阳化工大学制药与生物工程学院, 辽宁 沈阳 110142)])], figs=[ArticleFig(id=1194708178144301767, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=ENzZlFaGqEj2d7qfj57Vjg==, figureFileBig=wJhlkU+jlVLXxuRARFzN6w==, tableContent=null), ArticleFig(id=1194708178265936584, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Figure 1, caption=
Chemical structure of ursolic acid (UA) , figureFileSmall=ENzZlFaGqEj2d7qfj57Vjg==, figureFileBig=wJhlkU+jlVLXxuRARFzN6w==, tableContent=null), ArticleFig(id=1194708178374988489, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=d7adoOvFDkKlVaHhu/F91g==, figureFileBig=bPSxyabLXHzc/GqmRrPMcQ==, tableContent=null), ArticleFig(id=1194708178475651786, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Figure 2, caption=
Design of new ursolic acid derivatives , figureFileSmall=d7adoOvFDkKlVaHhu/F91g==, figureFileBig=bPSxyabLXHzc/GqmRrPMcQ==, tableContent=null), ArticleFig(id=1194708178555343563, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=HRVTwoAdRrRMb1VR6F3hXg==, figureFileBig=6vA41GZogQpL9dDSQBkE4g==, tableContent=null), ArticleFig(id=1194708178618258124, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Scheme 1, caption=
Synthesis route of the target compound Ⅰ1-Ⅰ5 and Ⅱ1-Ⅱ5. Reagents and conditions: (a) appropriate anhydride, DMAP, THF, rt; (b) propargyl bromide, K2CO3, DMF, 60 ℃; (c) R2Br, K2CO3, DMF, rt; (d) 3-butynoic acid, DCC, DMAP, CH2Cl2, rt; (e) aromatic azide, sodium ascorbate, CuSO4·5H2O, EtOH, rt , figureFileSmall=HRVTwoAdRrRMb1VR6F3hXg==, figureFileBig=6vA41GZogQpL9dDSQBkE4g==, tableContent=null), ArticleFig(id=1194708181067731662, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=KVhsM774c3KtF9mGIvtUXw==, figureFileBig=audbehKDOGc91KuIwGTO9A==, tableContent=null), ArticleFig(id=1194708181164200656, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Figure 3, caption=
The binding mode of derivative Ⅱ4 with c-Kit protein predicted by molecular docking , figureFileSmall=KVhsM774c3KtF9mGIvtUXw==, figureFileBig=audbehKDOGc91KuIwGTO9A==, tableContent=null), ArticleFig(id=1194708181302612690, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | Yield/% | Melting/℃ | ESI-MS m/z [M+H]+ |
| Ⅰ1 | 50.4 | 176.3-177.7 | 656.29 |
| Ⅰ2 | 49.2 | 175.0-176.3 | 671.24 |
| Ⅰ3 | 55.6 | 171.4-172.7 | 684.51 |
| Ⅰ4 | 57.5 | 172.8-174.2 | 698.62 |
| Ⅰ5 | 58.1 | 168.5-170.0 | 712.52 |
| Ⅱ1 | 48.2 | 169.5-170.4 | 670.52 |
| Ⅱ2 | 50.6 | 170.2-171.1 | 684.37 |
| Ⅱ3 | 47.2 | 167.8-168.5 | 698.79 |
| Ⅱ4 | 50.8 | 165.2-166.3 | 712.64 |
| Ⅱ5 | 46.1 | 162.7-163.8 | 726.82 |
), ArticleFig(id=1194708181373915860, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Table 1, caption=
Yield, melting point and MS data of the target compounds
, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | Yield/% | Melting/℃ | ESI-MS m/z [M+H]+ |
| Ⅰ1 | 50.4 | 176.3-177.7 | 656.29 |
| Ⅰ2 | 49.2 | 175.0-176.3 | 671.24 |
| Ⅰ3 | 55.6 | 171.4-172.7 | 684.51 |
| Ⅰ4 | 57.5 | 172.8-174.2 | 698.62 |
| Ⅰ5 | 58.1 | 168.5-170.0 | 712.52 |
| Ⅱ1 | 48.2 | 169.5-170.4 | 670.52 |
| Ⅱ2 | 50.6 | 170.2-171.1 | 684.37 |
| Ⅱ3 | 47.2 | 167.8-168.5 | 698.79 |
| Ⅱ4 | 50.8 | 165.2-166.3 | 712.64 |
| Ⅱ5 | 46.1 | 162.7-163.8 | 726.82 |
), ArticleFig(id=1194708181457801941, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | 1H NMR (600 MHz, CDCl3) | 13C NMR (150 MHz, CDCl3) |
| 3-1 | δH 5.28 (s, 1H, 12-H), 4.40 (t, J = 7.0 Hz, 1H, 3-H), 2.89 (dd, J = 11.2, 4.2 Hz, 1H, H-18), 2.97(s, 1H), 2.06 (s, 3H), 1.03-2.04 (m, 20H), 0.90-1.07 (m, 2 H), 1.05 (s, 3H), 0.93 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H), 0.79 (s, 3H) | δC 179.5, 172.6, 143.3, 123.8, 83.1, 81.0, 55.2, 52.0, 47.6, 46.4, 46.1, 43.0, 42.4, 40.2, 39.8, 38.2, 37.8, 35.7, 32.4, 31.5, 30.4, 29.2, 27.2, 25.0, 24.3, 23.8, 23.5, 23.4, 22.0, 19.6, 17.3, 16.7, 16.2 |
| 3-2 | δH 5.30 (s, 1H, 12-H), 4.45 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 12.0, 4.8 Hz, 1H, H-18), 2.95 (s, 1H), 2.27-2.30 (m, 2H), 1.01-2.07 (m, 20H), 0.97-1.09 (m, 2 H), 1.19 (s, 3H), 1.02 (s, 3H), 0.92 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.87 (s, 3H), 0.84 (s, 3H), 0.81 (s, 3H) | δC 179.0, 174.3, 143.9, 124.3, 82.4, 80.3, 55.6, 52.4, 47.3, 46.7, 46.5, 42.7, 42.1, 39.7, 39.1, 37.9, 37.6, 36.2, 32.9, 31.2, 29.4, 28.3, 26.7, 24.7, 24.0, 23.5, 23.4, 23.1, 21.6, 19.0, 17.7, 16.9, 16.4, 9.7 |
| 3-3 | δH 5.27 (s, 1H, 12-H), 4.42 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 10.6, 4.0 Hz, 1H, H-18), 2.98 (s, 1H), 1.83-2.35 (m, 4H), 1.05-2.02 (m, 20H), 0.95-1.12 (m, 2 H), 1.05 (s, 3H), 1.02 (s, 3H), 1.00 (s, 3H), 0.95 (s, 3H), 0.92 (s, 3H), 0.88 (s, 3H), 0.87 (s, 3H), 0.84 (s, 3H) | δC 179.7, 174.0, 140.1, 123.1, 83.5, 81.1, 55.0, 52.1, 47.5, 46.2, 43.1, 42.3, 40.1, 39.2, 38.7, 38.5, 37.2, 37.0, 36.2, 36.0, 33.2, 30.8, 28.8, 28.0, 27.2, 24.2, 23.8, 23.5, 23.0, 22.6, 21.6, 18.5, 18.1, 16.1, 14.0 |
| 3-4 | δH 5.32 (s, 1H, 12-H), 4.38 (t, J = 7.0 Hz, 1 H, 3-H), 2.85 (dd, J = 12.2, 4.6 Hz, 1H, H-18), 2.92 (s, 1H), 1.40-2.32 (m, 6H), 1.10-2.13 (m, 20H), 0.97-1.15 (m, 2H), 1.08 (s, 3H), 1.05 (s, 3H), 0.97 (s, 3H), 0.93 (s, 3H), 0.92 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.82 (s, 3H) | δC 180.2, 173.2, 139.5, 123.4, 83.7, 80.6, 55.6, 52.4, 47.1, 46.6, 42.8, 41.7, 41.2, 39.9, 38.2, 37.4, 37.0, 36.8, 36.4, 36.2, 34.2, 31.2, 29.3, 28.5, 26.9, 24.5, 23.8, 23.6, 23.1, 22.3, 21.2, 18.4, 17.7, 16.9, 16.6, 13.5 |
| 3-5 | δH 5.26 (s, 1H, 12-H), 4.38 (t, J = 7.0 Hz, 1H, 3-H), 2.85 (dd, J = 10.4, 4.0 Hz, 1H, H-18), 2.95 (s, 1H), 1.25-2.36 (m, 8H), 1.12-2.21 (m, 20H), 0.94-1.14 (m, 2H), 1.10 (s, 3H), 1.04 (s, 3H), 1.02 (s, 3H), 0.97 (s, 3H), 0.93 (s, 3H), 0.92 (s, 3H), 0.88 (s, 3H), 0.87 (s, 3H) | δC 180.0, 173.5, 138.2, 123.0, 84.0, 81.2, 55.2, 52.0, 47.7, 46.2, 43.1, 42.0, 40.6, 39.7, 39.2, 37.8, 37.5, 37.0, 36.4, 36.0, 33.7, 31.6, 31.2, 29.0, 28.9, 26.3, 24.1, 24.0, 23.8, 23.4, 22.1, 21.6, 18.1, 17.2, 16.7, 16.0, 14.2 |
| 5-1 | δH 5.32 (s, 1H, 12-H), 4.45 (t, J = 7.4 Hz, 1H, 3-H), 4.15-4.21 (m, 2H), 2.82 (s, 1H), 2.55 (dd, J = 10.8, 4.0 Hz, 1H, H-18), 1.10-2.11 (m, 20H), 1.23 (s, 3H), 1.10 (s, 3H), 1, 02 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.88 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H) | δC 177.5, 160.2, 140.2, 123.3, 84.1, 75.1, 74.6, 61.3, 55.7, 52.8, 48.6, 47.1, 42.8, 40.5, 39.5, 39.0, 38.9, 37.8, 37.5, 37.0, 33.2, 30.7, 29.1, 26.5, 24.6, 24.0, 23.8, 23.6, 23.2, 21.4, 18.9, 17.6, 17.0, 16.5, 15.1 |
| 5-2 | δH 5.28 (s, 1H, 12-H), 4.42 (t, J = 8.0 Hz, 1H, 3-H), 4.10-4.20 (m, 2H), 2.74 (s, 1H), 2.52 (dd, J = 9.4, 4.2 Hz, 1H, H-18), 1.06-2.14 (m, 20H), 1.68-1.74 (m, 2H), 1.10 (s, 3H), 1, 02 (s, 3H), 0.98 (s, 3H), 0.90 (s, H), 0.88 (s, 3H), 0.86 (s, 3H), 0.85 (s, 3H), 0.83 (s, 3H) | δC 177.0, 155.6, 139.1, 123.0, 83.5, 74.9, 73.8, 65.7, 55.7, 53.2, 48.6, 47.5, 42.2, 40.2, 39.1, 38.7, 38.5, 37.6, 37.3, 36.8, 33.5, 30.5, 29.4, 26.0, 24.3, 23.9, 23.7, 23.5, 23.0, 21.9, 21.4, 18.5, 17.6, 17.2, 16.2, 10.4 |
| 5-3 | δH 5.21 (s, 1H, 12-H), 4.40 (t, J = 8.2 Hz, 1H, 3-H), 4.05-4.12 (m, 2H), 2.70 (s, 1H), 2.50 (dd, J = 10.8, 4.4 Hz, 1H, H-18), 1.10-2.18 (m, 20H), 1.37-1.55 (m, 4H), 1.07 (s, 3H), 1, 03 (s, 3H), 1.01 (s, 3H), 0.92 (s, H), 0.90 (s, 3H), 0.88 (s, 3H), 0.86 (s, 3H), 0.81 (s, 3H) | δC 177.5, 154.0, 138.3, 123.4, 84.3, 74.5, 73.9, 65.3, 55.2, 53.7, 48.4, 47.2, 42.6, 40.5, 39.4, 39.2, 38.5, 37.8, 37.6, 35.9, 34.7, 32.4, 30.2, 28.8, 27.2, 24.5, 24.0, 23.5, 22.6, 22.3, 21.6, 21.5, 18.2, 18.1, 17.5, 16.4, 14.0 |
| 5-4 | δH 5.30 (s, 1H, 12-H), 4.42 (t, J = 7.6 Hz, 1H, 3-H), 4.02-4.10 (m, 2H), 2.74 (s, 1H), 2.56 (dd, J = 12.0, 4.4 Hz, 1H, H-18), 1.05-2.13 (m, 20H), 1.39-1.61 (m, 6H), 1.02 (s, 3H), 0.99 (s, 3H), 0.98 (s, 3H), 0.90 (s, H), 0.89 (s, 3H), 0.88 (s, 3H), 0.86 (s, 3H), 0.84 (s, 3H) | δC 177.2, 153.5, 138.0, 124.0, 83.8, 74.2, 73.9, 65.8, 55.6, 53.3, 49.2, 48.5, 44.1, 41.2, 40.2, 39.5, 39.2, 37.2, 36.4, 35.3, 34.2, 30.1, 29.0, 28.4, 27.9, 27.0, 24.3, 23.9, 22.8, 22.5, 22.1, 21.6, 21.4, 18.9, 18.8, 18.2, 16.2, 14.2 |
| 5-5 | δH 5.23 (s, 1H, 12-H), 4.46 (t, J = 7.0 Hz, 1H, 3-H), 4.02-4.08 (m, 2H), 2.70 (s, 1H), 2.56 (dd, J = 12.2, 4.8 Hz, 1H, H-18), 1.12-2.25 (m, 20H), 1.36-1.65 (m, 8H), 1.04 (s, 3H), 0.98 (s, 3H), 0.97 (s, 3H), 0.89 (s, H), 0.87 (s, 3H), 0.85 (s, 3H), 0.80 (s, 3H), 0.78 (s, 3H) | δC 177.6, 154.0, 138.5, 123.5, 84.2, 74.5, 74.0, 66.0, 56.2, 54.2, 50.1, 48.3, 45.4, 42.1, 41.8, 40.5, 39.7, 39.2, 38.2, 36.2, 35.1, 31.7, 29.3, 29.2, 28.4, 28.0, 27.5, 24.1, 23.6, 23.4, 22.7, 22.3, 21.5, 21.4, 19.3, 19.2, 18.6, 17.0, 12.7 |
| Ⅰ1 | δH 7.79 (s, 1H, triazole-H), 7.05-7.53 (m, 5H), 5.31 (s, 1H, 12-H), 5.20 (d, J = 2.0 Hz, 2H), 4.49 (t, J = 7.2 Hz, 1 H, 3-H), 2.93 (dd, J = 11.0, 4.6 Hz, 1H, H-18), 2.06 (s, 3H), 1.07-2.01 (m, 20H), 0.94-1.05 (m, 2H), 1.02 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.86 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H) | δC 179.5, 174.2, 144.7, 134.4, 131.2, 128.4, 128.4, 127.0, 127.0, 122.9, 80.4, 63.1, 55.1, 47.3, 46.7, 46.4, 43.1, 42.0, 39.3, 38.0, 37.7, 36.1, 35.8, 34.1, 32.8, 32.7, 32.2, 30.6, 29.8, 28.0, 27.9, 25.6, 25.6, 23.7, 23.5, 23.5, 21.1, 18.0, 16.9, 16.6, 15.3 |
| Ⅰ2 | δH 7.81 (s, 1H, triazole-H), 7.02-7.50 (m, 5H), 5.32 (s, 1H, 12-H), 5.19 (d, J = 3.2 Hz, 2H), 4.50 (t, J = 7.9 Hz, 1H, 3-H), 2.89 (dd, J = 9.2, 4.0 Hz, 1H, H-18), 2.31-2.27 (m, 2H), 1.04-2.05 (m, 20H), 1.22 (s, 3H), 0.94-1.07 (m, 2H), 1.01 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.87 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H), 0.80 (s, 3H) | δC 178.5, 171.0, 144.8, 132.3, 132.2, 126.1 126.1, 126.0, 126.0, 122.8, 115.8, 115.6, 80.8, 63.9, 55.1, 53.2, 47.4, 46.7, 46.5, 42.1, 42.0, 39.3, 38.8, 38.1, 37.7, 36.7, 34.1, 33.0, 32.6, 32.2, 28.0, 27.3, 25.7, 23.8, 23.6, 23.5, 23.4, 21.3, 18.1, 16.8, 16.6, 15.2 |
| Ⅰ3 | δH 7.84 (s, 1H, triazole-H), 7.05-7.58 (m, 5H), 5.32 (s, 1H, 12-H), 5.23 (d, J = 3.0 Hz, 2H), 4.52 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 8.0, 4.0 Hz, 1H, H-18), 2.35-2.29 (m, 2H), 1.06-2.01 (m, 20H), 1.61-1.68 (m, 2H), 1.60 (m, 2H), 1.23 (s, 3H), 1.15 (s, 3H), 0.95-1.07 (m, 2H), 0.94 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H), 0.84 (s, 3H), 0.78 (s, 3H) | δC 178.4, 170.9, 144.7, 132.7, 132.7, 132.7 132.2, 132.1, 127.7, 125.7, 125.7, 125.4, 125.4, 80.7, 55.0, 47.3, 46.6, 46.3, 42.0, 41.9, 39.2, 38.7, 38.0, 37.7, 37.5, 36.6, 32.8, 32.5, 32.1, 30.6, 27.9, 27.1, 26.8, 25.6, 23.7, 23.4, 23.4, 23.2, 21.2, 18.0, 16.7, 16.5, 15.1 |
| Ⅰ4 | δH 7.82 (s, 1H, triazole-H), 7.01-7.50 (m, 5H), 5.32 (s, 1H, 12-H), 5.21 (d, J = 3.4 Hz, 2H), 4.51 (t, J = 7.5 Hz, 1 H, 3-H), 2.83 (dd, J = 8.0, 4.0 Hz, 1H, H-18), 2.33-2.25 (m, 2H), 1.01-2.05 (m, 20H), 1.35-1.80 (m, 4H), 1.25 (s, 3H), 1.16 (s, 3H), 0.92-1.04 (m, 2 H), 1.02 (s, 3H), 0.92 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.86 (s, 3H), 0.79 (s, 3H) | δC 178.5, 174.3, 144.7, 138.7, 134.9, 132.7, 131.2, 128.0, 128.0, 127.2, 127.2, 122.9, 80.5, 64.6, 55.1, 47.4, 46.7, 46.4, 42.1, 42.1, 42.0, 39.3, 38.6, 38.1, 37.8, 36.8, 34.1, 33.0, 32.6, 32.2, 32.2, 30.7, 28.1, 28.0, 27.3, 23.8, 23.8, 23.5, 23.4, 21.2, 18.1, 16.8, 16.7, 15.3 |
| Ⅰ5 | δH 7.87 (s, 1H, triazole-H), 7.03-7.55 (m, 5H), 5.29 (s, 1H, 12-H), 5.19 (d, J = 3.2 Hz, 2H), 4.49 (t, J = 7.2 Hz, 1 H, 3-H), 2.82 (dd, J = 8.4, 4.3 Hz, 1H, H-18), 2.34-2.26 (m, 2H), 1.04-2.08 (m, 20H), 1.26-1.78 (m, 6H), 1.21 (s, 3H), 1.18 (s, 3H), 0.90-1.06 (m, 2 H), 0.96 (s, 3H), 0.93 (s, 3H), 0.89 (s, 3H), 0.86 (s, 3H), 0.85(s, 3H), 0.76 (s, 3H) | δC 179.7, 174.4, 144.9, 134.7, 131.4, 128.7, 128.7, 127.2, 127.2, 123.1, 80.6, 63.3, 55.3, 47.6, 46.9, 46.6, 42.2, 42.2, 39.5, 38.3, 37.9, 36.3, 36.0, 34.3, 33.1, 33.0, 32.4, 32.4, 30.8, 30.1, 28.2, 28.1, 27.5, 27.5, 25.8, 25.8, 23.9, 23.7, 23.6, 18.3, 17.1, 16.8, 16.8, 15.5, 9.5 |
| Ⅱ1 | δH 7.88 (s, 1H, triazole-H), 7.10-7.55 (m, 5H), 5.43 (s, 1H, 12-H), 4.41 (t, J = 8.0 Hz, 1H, 3-H), 4.25-4.19 (m, 2H), 3.63 (t, J = 7.2 Hz, 2H), 2.58 (dd, J = 12.0, 4.0 Hz, 1H, H-18), 1.01-2.02 (m, 20H), 1.20 (s, 3H), 1.15 (s, 3H), 0.92-1.08 (m, 2H), 0.98 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.84 (s, 3H), 0.80(s, 3H), 0.71 (s, 3H) | δC 179.5, 174.2, 144.7, 133.5, 131.2, 128.4, 128.4, 127.0, 127.0, 125.9, 125.9, 80.4, 64.4, 55.1, 47.4, 46.7, 46.4, 42.1, 42.0, 42.0, 39.3, 38.0, 37.7, 36.8, 36.1, 35.8, 32.9, 32.8, 32.2, 30.6, 29.9, 28.0, 27.9, 25.6, 23.7, 23.5, 23.4, 21.3, 21.1, 18.6, 16.9, 15.3 |
| Ⅱ2 | δH 7.83 (s, 1H, triazole-H), 7.03-7.53 (m, 5H), 5.21 (s, 1H, 12-H), 4.29 (t, J = 8.2 Hz, 1H, 3-H), 4.24-4.17 (m, 2H), 3.60 (t, J = 7.0 Hz, 2H), 2.55 (dd, J = 12.4, 3.5 Hz, 1H, H-18), 1.03-2.06 (m, 20H), 1.72 (m, 2 H), 1.19 (s, 3H), 1.14 (s, 3H), 0.90-1.10 (m, 2H), 0.98 (s, 3H), 0.93 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H) | δC 178.6, 171.2, 144.9, 132.4, 132.4 132.3, 132.3, 126.2, 126.2, 126.1, 125.9, 121.9, 121.9, 121.8, 80.9, 64.0, 55.2, 47.5, 46.9, 46.6, 42.2, 42.1, 39.4, 39.0, 37.8, 36.9, 34.2, 33.1, 32.7, 32.3, 30.8, 28.1, 27.3, 26.7, 25.8, 23.9, 23.6, 23.6, 23.5, 18.2, 16.9, 15.3, 9.33 |
| Ⅱ3 | δH 7.86 (s, 1H, triazole-H), 7.09-7.45 (m, 5H), 5.24 (s, 1H, 12-H), 4.23 (t, J = 8.2 Hz, 1 H, 3-H), 4.20-4.10 (m, 2H), 3.58 (t, J = 7.2 Hz, 2H), 2.52 (dd, J = 12.0, 4.5 Hz, 1H, H-18), 1.05-2.10 (m, 20H), 1.32-1.59 (m, 4H), 1.15 (s, 3H), 1.10 (s, 3H), 0.91-1.07 (m, 2H), 0.95 (s, 3H), 0.93 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.83 (s, 3H) | δC 179.4, 171.0, 144.7, 136.4, 134.2, 131.8, 130.7, 130.0, 130.0, 127.4, 127.4, 122.9, 121.4, 119.7, 80.8, 65.0, 55.2, 47.5, 46.7, 46.4, 42.1, 39.4, 39.4, 38.1, 37.7, 36.9, 36.5, 34.1, 30.7, 29.9, 29.9, 28.0, 27.3, 25.7, 25.7, 24.8, 23.7, 23.6, 23.6, 21.3, 18.2, 17.0, 16.7, 15.4 |
| Ⅱ4 | δH 7.84 (s, 1H, triazole-H), 7.13-7.50 (m, 5H), 5.31 (s, 1H, 12-H), 4.26 (t, J = 8.0 Hz, 1H, 3-H), 4.23-4.12 (m, 2H), 3.55 (t, J = 7.2 Hz, 2H), 2.50 (dd, J = 12.0, 4.0 Hz, 1H, H-18), 1.02-2.14 (m, 20H), 1.35-1.69 (m, 6H), 1.12 (s, 3H), 0.95-1.05 (m, 2H), 0.99 (s, 3H), 0.98 (s, 3H), 0.94 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.79 (s, 3H), 0.77 (s, 3H) | δC 179.6, 174.3, 144.8, 134.6, 131.3, 128.5, 128.5, 127.1, 127.1, 123.0, 80.5, 65.2, 55.2, 47.5, 46.8, 46.5, 42.1, 42.1, 39.4, 39.4, 38.1, 37.8, 36.9, 36.2, 35.9, 33.0, 32.9, 30.7, 30.0, 30.0, 28.1, 27.4, 26.8, 25.7, 25.7, 23.8, 23.6, 23.5, 18.2, 18.2, 17.0, 16.7, 15.4, 15.4, 9.4 |
| Ⅱ5 | δH 7.91 (s, 1H, triazole-H), 7.10-7.59 (m, 5H), 5.43 (s, 1H, 12-H), 4.32 (t, J = 8.2 Hz, 1H, 3-H), 4.30-4.16 (m, 2H), 3.58 (t, J = 7.2 Hz, 2H), 2.55 (dd, J = 12.4, 4.2 Hz, 1H, H-18), 1.01-2.07 (m, 20H), 1.28-1.65 (m, 8H), 1.10 (s, 3H), 0.94-1.06 (m, 2H), 0.99 (s, 3H), 0.98 (s, 3H), 0.97 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.79 (s, 3H), 0.75 (s, 3H) | δC 179.4, 171.1, 144.7, 136.4, 134.2, 131.8, 130.7, 130.7, 130.0, 130.0, 127.4, 127.4, 122.9, 80.9, 66.2, 55.2, 47.5, 46.7, 46.4, 42.1, 42.1, 42.0, 39.4, 38.1, 37.7, 36.9, 36.5, 34.1, 33.0, 32.9, 32.9, 30.7, 30.0, 28.0, 27.3, 25.7, 24.8, 23.7, 21.3, 21.3, 18.2, 17.0, 16.7, 15.4, 15.4, 9.4 |
), ArticleFig(id=1194708181541688022, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Table 2, caption=
Spectral data of the compounds 3-1-3-5, 5-1-5-5, Ⅰ1-Ⅰ5, Ⅱ1-Ⅱ5
, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | 1H NMR (600 MHz, CDCl3) | 13C NMR (150 MHz, CDCl3) |
| 3-1 | δH 5.28 (s, 1H, 12-H), 4.40 (t, J = 7.0 Hz, 1H, 3-H), 2.89 (dd, J = 11.2, 4.2 Hz, 1H, H-18), 2.97(s, 1H), 2.06 (s, 3H), 1.03-2.04 (m, 20H), 0.90-1.07 (m, 2 H), 1.05 (s, 3H), 0.93 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H), 0.79 (s, 3H) | δC 179.5, 172.6, 143.3, 123.8, 83.1, 81.0, 55.2, 52.0, 47.6, 46.4, 46.1, 43.0, 42.4, 40.2, 39.8, 38.2, 37.8, 35.7, 32.4, 31.5, 30.4, 29.2, 27.2, 25.0, 24.3, 23.8, 23.5, 23.4, 22.0, 19.6, 17.3, 16.7, 16.2 |
| 3-2 | δH 5.30 (s, 1H, 12-H), 4.45 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 12.0, 4.8 Hz, 1H, H-18), 2.95 (s, 1H), 2.27-2.30 (m, 2H), 1.01-2.07 (m, 20H), 0.97-1.09 (m, 2 H), 1.19 (s, 3H), 1.02 (s, 3H), 0.92 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.87 (s, 3H), 0.84 (s, 3H), 0.81 (s, 3H) | δC 179.0, 174.3, 143.9, 124.3, 82.4, 80.3, 55.6, 52.4, 47.3, 46.7, 46.5, 42.7, 42.1, 39.7, 39.1, 37.9, 37.6, 36.2, 32.9, 31.2, 29.4, 28.3, 26.7, 24.7, 24.0, 23.5, 23.4, 23.1, 21.6, 19.0, 17.7, 16.9, 16.4, 9.7 |
| 3-3 | δH 5.27 (s, 1H, 12-H), 4.42 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 10.6, 4.0 Hz, 1H, H-18), 2.98 (s, 1H), 1.83-2.35 (m, 4H), 1.05-2.02 (m, 20H), 0.95-1.12 (m, 2 H), 1.05 (s, 3H), 1.02 (s, 3H), 1.00 (s, 3H), 0.95 (s, 3H), 0.92 (s, 3H), 0.88 (s, 3H), 0.87 (s, 3H), 0.84 (s, 3H) | δC 179.7, 174.0, 140.1, 123.1, 83.5, 81.1, 55.0, 52.1, 47.5, 46.2, 43.1, 42.3, 40.1, 39.2, 38.7, 38.5, 37.2, 37.0, 36.2, 36.0, 33.2, 30.8, 28.8, 28.0, 27.2, 24.2, 23.8, 23.5, 23.0, 22.6, 21.6, 18.5, 18.1, 16.1, 14.0 |
| 3-4 | δH 5.32 (s, 1H, 12-H), 4.38 (t, J = 7.0 Hz, 1 H, 3-H), 2.85 (dd, J = 12.2, 4.6 Hz, 1H, H-18), 2.92 (s, 1H), 1.40-2.32 (m, 6H), 1.10-2.13 (m, 20H), 0.97-1.15 (m, 2H), 1.08 (s, 3H), 1.05 (s, 3H), 0.97 (s, 3H), 0.93 (s, 3H), 0.92 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.82 (s, 3H) | δC 180.2, 173.2, 139.5, 123.4, 83.7, 80.6, 55.6, 52.4, 47.1, 46.6, 42.8, 41.7, 41.2, 39.9, 38.2, 37.4, 37.0, 36.8, 36.4, 36.2, 34.2, 31.2, 29.3, 28.5, 26.9, 24.5, 23.8, 23.6, 23.1, 22.3, 21.2, 18.4, 17.7, 16.9, 16.6, 13.5 |
| 3-5 | δH 5.26 (s, 1H, 12-H), 4.38 (t, J = 7.0 Hz, 1H, 3-H), 2.85 (dd, J = 10.4, 4.0 Hz, 1H, H-18), 2.95 (s, 1H), 1.25-2.36 (m, 8H), 1.12-2.21 (m, 20H), 0.94-1.14 (m, 2H), 1.10 (s, 3H), 1.04 (s, 3H), 1.02 (s, 3H), 0.97 (s, 3H), 0.93 (s, 3H), 0.92 (s, 3H), 0.88 (s, 3H), 0.87 (s, 3H) | δC 180.0, 173.5, 138.2, 123.0, 84.0, 81.2, 55.2, 52.0, 47.7, 46.2, 43.1, 42.0, 40.6, 39.7, 39.2, 37.8, 37.5, 37.0, 36.4, 36.0, 33.7, 31.6, 31.2, 29.0, 28.9, 26.3, 24.1, 24.0, 23.8, 23.4, 22.1, 21.6, 18.1, 17.2, 16.7, 16.0, 14.2 |
| 5-1 | δH 5.32 (s, 1H, 12-H), 4.45 (t, J = 7.4 Hz, 1H, 3-H), 4.15-4.21 (m, 2H), 2.82 (s, 1H), 2.55 (dd, J = 10.8, 4.0 Hz, 1H, H-18), 1.10-2.11 (m, 20H), 1.23 (s, 3H), 1.10 (s, 3H), 1, 02 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.88 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H) | δC 177.5, 160.2, 140.2, 123.3, 84.1, 75.1, 74.6, 61.3, 55.7, 52.8, 48.6, 47.1, 42.8, 40.5, 39.5, 39.0, 38.9, 37.8, 37.5, 37.0, 33.2, 30.7, 29.1, 26.5, 24.6, 24.0, 23.8, 23.6, 23.2, 21.4, 18.9, 17.6, 17.0, 16.5, 15.1 |
| 5-2 | δH 5.28 (s, 1H, 12-H), 4.42 (t, J = 8.0 Hz, 1H, 3-H), 4.10-4.20 (m, 2H), 2.74 (s, 1H), 2.52 (dd, J = 9.4, 4.2 Hz, 1H, H-18), 1.06-2.14 (m, 20H), 1.68-1.74 (m, 2H), 1.10 (s, 3H), 1, 02 (s, 3H), 0.98 (s, 3H), 0.90 (s, H), 0.88 (s, 3H), 0.86 (s, 3H), 0.85 (s, 3H), 0.83 (s, 3H) | δC 177.0, 155.6, 139.1, 123.0, 83.5, 74.9, 73.8, 65.7, 55.7, 53.2, 48.6, 47.5, 42.2, 40.2, 39.1, 38.7, 38.5, 37.6, 37.3, 36.8, 33.5, 30.5, 29.4, 26.0, 24.3, 23.9, 23.7, 23.5, 23.0, 21.9, 21.4, 18.5, 17.6, 17.2, 16.2, 10.4 |
| 5-3 | δH 5.21 (s, 1H, 12-H), 4.40 (t, J = 8.2 Hz, 1H, 3-H), 4.05-4.12 (m, 2H), 2.70 (s, 1H), 2.50 (dd, J = 10.8, 4.4 Hz, 1H, H-18), 1.10-2.18 (m, 20H), 1.37-1.55 (m, 4H), 1.07 (s, 3H), 1, 03 (s, 3H), 1.01 (s, 3H), 0.92 (s, H), 0.90 (s, 3H), 0.88 (s, 3H), 0.86 (s, 3H), 0.81 (s, 3H) | δC 177.5, 154.0, 138.3, 123.4, 84.3, 74.5, 73.9, 65.3, 55.2, 53.7, 48.4, 47.2, 42.6, 40.5, 39.4, 39.2, 38.5, 37.8, 37.6, 35.9, 34.7, 32.4, 30.2, 28.8, 27.2, 24.5, 24.0, 23.5, 22.6, 22.3, 21.6, 21.5, 18.2, 18.1, 17.5, 16.4, 14.0 |
| 5-4 | δH 5.30 (s, 1H, 12-H), 4.42 (t, J = 7.6 Hz, 1H, 3-H), 4.02-4.10 (m, 2H), 2.74 (s, 1H), 2.56 (dd, J = 12.0, 4.4 Hz, 1H, H-18), 1.05-2.13 (m, 20H), 1.39-1.61 (m, 6H), 1.02 (s, 3H), 0.99 (s, 3H), 0.98 (s, 3H), 0.90 (s, H), 0.89 (s, 3H), 0.88 (s, 3H), 0.86 (s, 3H), 0.84 (s, 3H) | δC 177.2, 153.5, 138.0, 124.0, 83.8, 74.2, 73.9, 65.8, 55.6, 53.3, 49.2, 48.5, 44.1, 41.2, 40.2, 39.5, 39.2, 37.2, 36.4, 35.3, 34.2, 30.1, 29.0, 28.4, 27.9, 27.0, 24.3, 23.9, 22.8, 22.5, 22.1, 21.6, 21.4, 18.9, 18.8, 18.2, 16.2, 14.2 |
| 5-5 | δH 5.23 (s, 1H, 12-H), 4.46 (t, J = 7.0 Hz, 1H, 3-H), 4.02-4.08 (m, 2H), 2.70 (s, 1H), 2.56 (dd, J = 12.2, 4.8 Hz, 1H, H-18), 1.12-2.25 (m, 20H), 1.36-1.65 (m, 8H), 1.04 (s, 3H), 0.98 (s, 3H), 0.97 (s, 3H), 0.89 (s, H), 0.87 (s, 3H), 0.85 (s, 3H), 0.80 (s, 3H), 0.78 (s, 3H) | δC 177.6, 154.0, 138.5, 123.5, 84.2, 74.5, 74.0, 66.0, 56.2, 54.2, 50.1, 48.3, 45.4, 42.1, 41.8, 40.5, 39.7, 39.2, 38.2, 36.2, 35.1, 31.7, 29.3, 29.2, 28.4, 28.0, 27.5, 24.1, 23.6, 23.4, 22.7, 22.3, 21.5, 21.4, 19.3, 19.2, 18.6, 17.0, 12.7 |
| Ⅰ1 | δH 7.79 (s, 1H, triazole-H), 7.05-7.53 (m, 5H), 5.31 (s, 1H, 12-H), 5.20 (d, J = 2.0 Hz, 2H), 4.49 (t, J = 7.2 Hz, 1 H, 3-H), 2.93 (dd, J = 11.0, 4.6 Hz, 1H, H-18), 2.06 (s, 3H), 1.07-2.01 (m, 20H), 0.94-1.05 (m, 2H), 1.02 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.86 (s, 3H), 0.85 (s, 3H), 0.82 (s, 3H) | δC 179.5, 174.2, 144.7, 134.4, 131.2, 128.4, 128.4, 127.0, 127.0, 122.9, 80.4, 63.1, 55.1, 47.3, 46.7, 46.4, 43.1, 42.0, 39.3, 38.0, 37.7, 36.1, 35.8, 34.1, 32.8, 32.7, 32.2, 30.6, 29.8, 28.0, 27.9, 25.6, 25.6, 23.7, 23.5, 23.5, 21.1, 18.0, 16.9, 16.6, 15.3 |
| Ⅰ2 | δH 7.81 (s, 1H, triazole-H), 7.02-7.50 (m, 5H), 5.32 (s, 1H, 12-H), 5.19 (d, J = 3.2 Hz, 2H), 4.50 (t, J = 7.9 Hz, 1H, 3-H), 2.89 (dd, J = 9.2, 4.0 Hz, 1H, H-18), 2.31-2.27 (m, 2H), 1.04-2.05 (m, 20H), 1.22 (s, 3H), 0.94-1.07 (m, 2H), 1.01 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.87 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H), 0.80 (s, 3H) | δC 178.5, 171.0, 144.8, 132.3, 132.2, 126.1 126.1, 126.0, 126.0, 122.8, 115.8, 115.6, 80.8, 63.9, 55.1, 53.2, 47.4, 46.7, 46.5, 42.1, 42.0, 39.3, 38.8, 38.1, 37.7, 36.7, 34.1, 33.0, 32.6, 32.2, 28.0, 27.3, 25.7, 23.8, 23.6, 23.5, 23.4, 21.3, 18.1, 16.8, 16.6, 15.2 |
| Ⅰ3 | δH 7.84 (s, 1H, triazole-H), 7.05-7.58 (m, 5H), 5.32 (s, 1H, 12-H), 5.23 (d, J = 3.0 Hz, 2H), 4.52 (t, J = 7.2 Hz, 1H, 3-H), 2.85 (dd, J = 8.0, 4.0 Hz, 1H, H-18), 2.35-2.29 (m, 2H), 1.06-2.01 (m, 20H), 1.61-1.68 (m, 2H), 1.60 (m, 2H), 1.23 (s, 3H), 1.15 (s, 3H), 0.95-1.07 (m, 2H), 0.94 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H), 0.84 (s, 3H), 0.78 (s, 3H) | δC 178.4, 170.9, 144.7, 132.7, 132.7, 132.7 132.2, 132.1, 127.7, 125.7, 125.7, 125.4, 125.4, 80.7, 55.0, 47.3, 46.6, 46.3, 42.0, 41.9, 39.2, 38.7, 38.0, 37.7, 37.5, 36.6, 32.8, 32.5, 32.1, 30.6, 27.9, 27.1, 26.8, 25.6, 23.7, 23.4, 23.4, 23.2, 21.2, 18.0, 16.7, 16.5, 15.1 |
| Ⅰ4 | δH 7.82 (s, 1H, triazole-H), 7.01-7.50 (m, 5H), 5.32 (s, 1H, 12-H), 5.21 (d, J = 3.4 Hz, 2H), 4.51 (t, J = 7.5 Hz, 1 H, 3-H), 2.83 (dd, J = 8.0, 4.0 Hz, 1H, H-18), 2.33-2.25 (m, 2H), 1.01-2.05 (m, 20H), 1.35-1.80 (m, 4H), 1.25 (s, 3H), 1.16 (s, 3H), 0.92-1.04 (m, 2 H), 1.02 (s, 3H), 0.92 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.86 (s, 3H), 0.79 (s, 3H) | δC 178.5, 174.3, 144.7, 138.7, 134.9, 132.7, 131.2, 128.0, 128.0, 127.2, 127.2, 122.9, 80.5, 64.6, 55.1, 47.4, 46.7, 46.4, 42.1, 42.1, 42.0, 39.3, 38.6, 38.1, 37.8, 36.8, 34.1, 33.0, 32.6, 32.2, 32.2, 30.7, 28.1, 28.0, 27.3, 23.8, 23.8, 23.5, 23.4, 21.2, 18.1, 16.8, 16.7, 15.3 |
| Ⅰ5 | δH 7.87 (s, 1H, triazole-H), 7.03-7.55 (m, 5H), 5.29 (s, 1H, 12-H), 5.19 (d, J = 3.2 Hz, 2H), 4.49 (t, J = 7.2 Hz, 1 H, 3-H), 2.82 (dd, J = 8.4, 4.3 Hz, 1H, H-18), 2.34-2.26 (m, 2H), 1.04-2.08 (m, 20H), 1.26-1.78 (m, 6H), 1.21 (s, 3H), 1.18 (s, 3H), 0.90-1.06 (m, 2 H), 0.96 (s, 3H), 0.93 (s, 3H), 0.89 (s, 3H), 0.86 (s, 3H), 0.85(s, 3H), 0.76 (s, 3H) | δC 179.7, 174.4, 144.9, 134.7, 131.4, 128.7, 128.7, 127.2, 127.2, 123.1, 80.6, 63.3, 55.3, 47.6, 46.9, 46.6, 42.2, 42.2, 39.5, 38.3, 37.9, 36.3, 36.0, 34.3, 33.1, 33.0, 32.4, 32.4, 30.8, 30.1, 28.2, 28.1, 27.5, 27.5, 25.8, 25.8, 23.9, 23.7, 23.6, 18.3, 17.1, 16.8, 16.8, 15.5, 9.5 |
| Ⅱ1 | δH 7.88 (s, 1H, triazole-H), 7.10-7.55 (m, 5H), 5.43 (s, 1H, 12-H), 4.41 (t, J = 8.0 Hz, 1H, 3-H), 4.25-4.19 (m, 2H), 3.63 (t, J = 7.2 Hz, 2H), 2.58 (dd, J = 12.0, 4.0 Hz, 1H, H-18), 1.01-2.02 (m, 20H), 1.20 (s, 3H), 1.15 (s, 3H), 0.92-1.08 (m, 2H), 0.98 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.84 (s, 3H), 0.80(s, 3H), 0.71 (s, 3H) | δC 179.5, 174.2, 144.7, 133.5, 131.2, 128.4, 128.4, 127.0, 127.0, 125.9, 125.9, 80.4, 64.4, 55.1, 47.4, 46.7, 46.4, 42.1, 42.0, 42.0, 39.3, 38.0, 37.7, 36.8, 36.1, 35.8, 32.9, 32.8, 32.2, 30.6, 29.9, 28.0, 27.9, 25.6, 23.7, 23.5, 23.4, 21.3, 21.1, 18.6, 16.9, 15.3 |
| Ⅱ2 | δH 7.83 (s, 1H, triazole-H), 7.03-7.53 (m, 5H), 5.21 (s, 1H, 12-H), 4.29 (t, J = 8.2 Hz, 1H, 3-H), 4.24-4.17 (m, 2H), 3.60 (t, J = 7.0 Hz, 2H), 2.55 (dd, J = 12.4, 3.5 Hz, 1H, H-18), 1.03-2.06 (m, 20H), 1.72 (m, 2 H), 1.19 (s, 3H), 1.14 (s, 3H), 0.90-1.10 (m, 2H), 0.98 (s, 3H), 0.93 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.85 (s, 3H) | δC 178.6, 171.2, 144.9, 132.4, 132.4 132.3, 132.3, 126.2, 126.2, 126.1, 125.9, 121.9, 121.9, 121.8, 80.9, 64.0, 55.2, 47.5, 46.9, 46.6, 42.2, 42.1, 39.4, 39.0, 37.8, 36.9, 34.2, 33.1, 32.7, 32.3, 30.8, 28.1, 27.3, 26.7, 25.8, 23.9, 23.6, 23.6, 23.5, 18.2, 16.9, 15.3, 9.33 |
| Ⅱ3 | δH 7.86 (s, 1H, triazole-H), 7.09-7.45 (m, 5H), 5.24 (s, 1H, 12-H), 4.23 (t, J = 8.2 Hz, 1 H, 3-H), 4.20-4.10 (m, 2H), 3.58 (t, J = 7.2 Hz, 2H), 2.52 (dd, J = 12.0, 4.5 Hz, 1H, H-18), 1.05-2.10 (m, 20H), 1.32-1.59 (m, 4H), 1.15 (s, 3H), 1.10 (s, 3H), 0.91-1.07 (m, 2H), 0.95 (s, 3H), 0.93 (s, 3H), 0.90 (s, 3H), 0.89 (s, 3H), 0.87 (s, 3H), 0.83 (s, 3H) | δC 179.4, 171.0, 144.7, 136.4, 134.2, 131.8, 130.7, 130.0, 130.0, 127.4, 127.4, 122.9, 121.4, 119.7, 80.8, 65.0, 55.2, 47.5, 46.7, 46.4, 42.1, 39.4, 39.4, 38.1, 37.7, 36.9, 36.5, 34.1, 30.7, 29.9, 29.9, 28.0, 27.3, 25.7, 25.7, 24.8, 23.7, 23.6, 23.6, 21.3, 18.2, 17.0, 16.7, 15.4 |
| Ⅱ4 | δH 7.84 (s, 1H, triazole-H), 7.13-7.50 (m, 5H), 5.31 (s, 1H, 12-H), 4.26 (t, J = 8.0 Hz, 1H, 3-H), 4.23-4.12 (m, 2H), 3.55 (t, J = 7.2 Hz, 2H), 2.50 (dd, J = 12.0, 4.0 Hz, 1H, H-18), 1.02-2.14 (m, 20H), 1.35-1.69 (m, 6H), 1.12 (s, 3H), 0.95-1.05 (m, 2H), 0.99 (s, 3H), 0.98 (s, 3H), 0.94 (s, 3H), 0.91 (s, 3H), 0.89 (s, 3H), 0.79 (s, 3H), 0.77 (s, 3H) | δC 179.6, 174.3, 144.8, 134.6, 131.3, 128.5, 128.5, 127.1, 127.1, 123.0, 80.5, 65.2, 55.2, 47.5, 46.8, 46.5, 42.1, 42.1, 39.4, 39.4, 38.1, 37.8, 36.9, 36.2, 35.9, 33.0, 32.9, 30.7, 30.0, 30.0, 28.1, 27.4, 26.8, 25.7, 25.7, 23.8, 23.6, 23.5, 18.2, 18.2, 17.0, 16.7, 15.4, 15.4, 9.4 |
| Ⅱ5 | δH 7.91 (s, 1H, triazole-H), 7.10-7.59 (m, 5H), 5.43 (s, 1H, 12-H), 4.32 (t, J = 8.2 Hz, 1H, 3-H), 4.30-4.16 (m, 2H), 3.58 (t, J = 7.2 Hz, 2H), 2.55 (dd, J = 12.4, 4.2 Hz, 1H, H-18), 1.01-2.07 (m, 20H), 1.28-1.65 (m, 8H), 1.10 (s, 3H), 0.94-1.06 (m, 2H), 0.99 (s, 3H), 0.98 (s, 3H), 0.97 (s, 3H), 0.91 (s, 3H), 0.90 (s, 3H), 0.79 (s, 3H), 0.75 (s, 3H) | δC 179.4, 171.1, 144.7, 136.4, 134.2, 131.8, 130.7, 130.7, 130.0, 130.0, 127.4, 127.4, 122.9, 80.9, 66.2, 55.2, 47.5, 46.7, 46.4, 42.1, 42.1, 42.0, 39.4, 38.1, 37.7, 36.9, 36.5, 34.1, 33.0, 32.9, 32.9, 30.7, 30.0, 28.0, 27.3, 25.7, 24.8, 23.7, 21.3, 21.3, 18.2, 17.0, 16.7, 15.4, 15.4, 9.4 |
), ArticleFig(id=1194708181671711447, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | IC50/μmol·L-1 | | Compd. | IC50/μmol·L-1 |
| MCF-7 | SGC-7901 | MCF-7 | SGC-7901 |
| Ⅰ1 | 40.22 ± 0.11 | 37.02 ± 0.07 | | Ⅱ1 | 39.27 ± 0.19 | 30.18 ± 0.22 |
| Ⅰ2 | 31.48 ± 0.10 | 20.13 ± 0.13 | Ⅱ2 | 33.32 ± 0.15 | 21.45 ± 0.08 |
| Ⅰ3 | 30.15 ± 0.15 | 19.21 ± 0.13 | Ⅱ3 | 23.13 ± 0.20 | 20.28 ± 0.15 |
| Ⅰ4 | 18.22 ± 0.09 | 12.72 ± 0.15 | Ⅱ4 | 14.28 ± 0.14 | 8.46 ± 0.10 |
| Ⅰ5 | 38.65 ± 0.16 | 25.12 ± 0.08 | Ⅱ5 | 20.68 ± 0.19 | 19.54 ± 0.17 |
| UA | > 50 | > 50 | Nilotinib | 15.40 ± 0.10 | 10.15 ± 0.08 |
), ArticleFig(id=1194708181763986136, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Table 3, caption=
Antitumor activity of different derivatives on cancer cells MCF-7 and SGC-7901
, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | IC50/μmol·L-1 | | Compd. | IC50/μmol·L-1 |
| MCF-7 | SGC-7901 | MCF-7 | SGC-7901 |
| Ⅰ1 | 40.22 ± 0.11 | 37.02 ± 0.07 | | Ⅱ1 | 39.27 ± 0.19 | 30.18 ± 0.22 |
| Ⅰ2 | 31.48 ± 0.10 | 20.13 ± 0.13 | Ⅱ2 | 33.32 ± 0.15 | 21.45 ± 0.08 |
| Ⅰ3 | 30.15 ± 0.15 | 19.21 ± 0.13 | Ⅱ3 | 23.13 ± 0.20 | 20.28 ± 0.15 |
| Ⅰ4 | 18.22 ± 0.09 | 12.72 ± 0.15 | Ⅱ4 | 14.28 ± 0.14 | 8.46 ± 0.10 |
| Ⅰ5 | 38.65 ± 0.16 | 25.12 ± 0.08 | Ⅱ5 | 20.68 ± 0.19 | 19.54 ± 0.17 |
| UA | > 50 | > 50 | Nilotinib | 15.40 ± 0.10 | 10.15 ± 0.08 |
), ArticleFig(id=1194708181835289305, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | Docking score | | Compd. | Docking score |
| Ⅰ1 | -154.697 | | Ⅱ1 | -155.338 |
| Ⅰ2 | -162.983 | Ⅱ2 | -160.921 |
| Ⅰ3 | -162.793 | Ⅱ3 | -161.544 |
| Ⅰ4 | -167.873 | Ⅱ4 | -172.941 |
| Ⅰ5 | -161.868 | Ⅱ5 | -165.844 |
| Nilotinib | -170.459 | UA | -120.341 |
), ArticleFig(id=1194708181898203866, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1193632556458406381, language=CN, label=Table 4, caption=
Docking analysis of ursolic acid derivatives and c-Kit protein
, figureFileSmall=null, figureFileBig=null, tableContent=
| Compd. | Docking score | | Compd. | Docking score |
| Ⅰ1 | -154.697 | | Ⅱ1 | -155.338 |
| Ⅰ2 | -162.983 | Ⅱ2 | -160.921 |
| Ⅰ3 | -162.793 | Ⅱ3 | -161.544 |
| Ⅰ4 | -167.873 | Ⅱ4 | -172.941 |
| Ⅰ5 | -161.868 | Ⅱ5 | -165.844 |
| Nilotinib | -170.459 | UA | -120.341 |
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