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Total synthesis and biological evaluation of dracaenins A and B
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Yaqiu Zhaoa, c, Shunli Xiaoc, Yun Youc, Zhi Zhangb, *, Liansuo Zub, *, Luqi Huangc, *
Chinese Chemical Letters | 2022, 33(5) : 2433 - 2436
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Chinese Chemical Letters | 2022, 33(5): 2433-2436
• Communication •
Total synthesis and biological evaluation of dracaenins A and B
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Yaqiu Zhaoa, c, Shunli Xiaoc, Yun Youc, Zhi Zhangb, *, Liansuo Zub, *, Luqi Huangc, *
Affiliations
  • aCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China
  • bSchool of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China
  • cState Key Laboratory Breeding Base of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China
Published: 2022-05-15 doi: 10.1016/j.cclet.2021.10.067
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The first total synthesis of dracaenins A and B is achieved in four steps. The synthesis features the convergent coupling of three readily available fragments with minimized use of protecting groups. The chemical synthesis enables the discovery of their activity in stimulating platelet aggregation, and thus, sheds light on the possible origin of the hemostatic effect of dragon's blood.

Total synthesis  /  Natural product  /  Dragon's blood  /  Dracaenin  /  Hemostasis
Yaqiu Zhao, Shunli Xiao, Yun You, Zhi Zhang, Liansuo Zu, Luqi Huang. Total synthesis and biological evaluation of dracaenins A and B[J]. Chinese Chemical Letters, 2022 , 33 (5) : 2433 -2436 . DOI: 10.1016/j.cclet.2021.10.067
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Dragon's blood refers to the red resinous exudations from plant species and has been used as herbal medicine for more than 1500 years across many cultures. Modern pharmacological studies of dragon's blood have revealed a wide array of bioactivities [1]. Among them, it has been highlighted to have bidirectional regulatory effect of stimulating both blood circulation and coagulation. The clarification and identification of active components that account for these contrasting activities are crucial for the in-depth studies of this important herbal medicine. In this context, several phenolic compounds [2-4], such as loureirin B (5) and cochinchinenin A (6), isolated from dragon's blood, have been shown to have the activity of promoting blood circulation (Fig. 1). However, the active components that could stimulate blood coagulation (hemostatic effect) remain to be discovered.
Dracaenins A (1) and B (2) were isolated from the Chinese dragon's blood, Dracaena cochinchinensis (Lour.) S.C. Chen, by Zhang and co-workers in 2012 (Fig. 1) [5]. Structurally, they feature the unusual chalcane-anthocyanidin dimers. Several anthocyanidins, such as dracorhodin (3) and nordracorhodin (4), have been isolated from dragon's blood and are known to account for its intense red color (Fig. 1). The related dihydrochalcones 5 and 6 have been reported to be able to inhibit platelet aggregation. Thus, the generation of such chalcane-anthocyanidin dimers by nature would be inspiring and useful as chemical probes to study the related biological activities.
The isolation yield of dracaenin A from dragon's blood is very low (23 mg dracaenin A was isolated from 3.0 kg of dragon's blood). In addition, this herbal medicine is very expensive due to its beneficial values to human health, the wide usage and the shortage of natural sources. Total synthesis has long been a powerful tool in facilitating the biological studies of natural products by providing enough materials particularly when the nature supply is limited or not accessible [6]. In addition, once the therapeutic potential of a natural product is identified, efficient chemical synthesis could offer a sustainable alternative for its production, thus alleviating the pressure on natural resource. While the structural complexity of dracaenins A and B is moderate, the concise assembly of these structures is not trivial. Attention should be paid to the electrophilicity of the anthocyanidin part in a synthetic design as demonstrated by the transformation of 3 to other more complex natural products by the group of Trauner [7]. Moreover, there are 7 phenolic oxygens with varied substitution patterns and oxidation state. The successful introduction of them with minimal reliance on protecting groups is crucial for synthetic efficiency [8]. Site-selectivity regarding the formation of the anthocyanidin part and chalcane-anthocyanidin connection are further concerns. Herein, we report our efforts to address these synthetic issues, which lead to the concise and convergent total synthesis of dracaenins A and B on only four steps. The chemical synthesis further enables the discovery of their activity in stimulating platelet aggregation, and thus, sheds light on the possible origin of the hemostatic effect of dragon's blood.
It could be envisioned from the outset that a successful synthesis would afford dracaenins A and B in short synthetic sequence, in a convergent manner [9] and with the minimized use of protecting groups [8]. To fulfill these standards, our synthetic plan was depicted in Scheme 1. We surmised that the chalcane-anthocyanidin connection of dracaenins A and B could be furnished by the direct Friedel-Crafts coupling of alcohol 7 and phloroglucinol derivative 8. It was hoped that the coupling could proceed without any protecting groups on the phenolic oxygens. Regarding the synthesis of the anthocyanidin part, several known methods have been reported [7, 10, 11]. The most common approach requires the pre-functionalization of the precursor, for example the coupling products of 7 and 8, with an aldehyde group as the synthetic handle. We envisioned that such stepwise operations would pose significant challenges in controlling the chemoselectivity without using protecting groups. Thus, we turned to a direct annulation approach developed by the group of Chassaing using ethynyl ketone 9 [12, 13]. In our synthetic plan, only ethynyl ketone 9 was protected as the TBS ether, which was introduced during its preparation and could be concomitantly cleaved under the acidic annulation conditions. In addition, our synthetic design features the convergent coupling of three fragments 7–9, which could allow for the synthesis of structural analogs, if necessary, by the facile variation of these fragments.
We first selected dracaenin B as our synthetic target (Scheme 2). The coupling partner 7b was successfully synthesized in 2 steps by the Aldol type condensation of 10 and 11 followed by hydrogenation of the resulting chalcone. The coupling of 7b and phloroglucinol derivative 8 turned out to be challenging. Different acids that could potentially promote the Friedel-Crafts alkylation were screened (Table 1). In the presence of HCl or p-TsOH, the formation of the desired product was not observed. The switch to BF3·Et2O [14, 15] at −10 ℃ led to the production of 12 in synthetically useful yield (48%; entry 4), albeit companied with its regio-isomer 12′ (12:12′ = 1.6:1). The use of diphenyl phosphate as the acidic promotor in acetonitrile gave similar yield of 12 with slightly lower site-selectivity (entry 6). In the current investigation, we chose to use the BF3·Et2O condition for the synthesis of 12.
Finally, we turned to the direct annulation of 12 and 9 to afford the anthocyanidin moiety. The literature conditions using stoichiometric amount of HPF6 gave less than 5% formation of the PF6- salt of dracaenin B [12, 13]. After further examination of the reaction mixture, the formation of 13 was observed as the major by product, indicating that the retro-Friedel-Crafts type cleavage occurred under the strong acidic conditions. While this side reaction pathway could be potentially inhibited by the appendant of suitable protecting groups, we did not prefer such a strategy as it would hurt the step economy of the synthesis [16]. After systematic investigation of the amount of HPF6 and the reaction concentration, we found dracaenin B could be formed in 40% yield in the presence of 12 mol% HPF6 and at diluted concentration. Analogously, dracaenin A was produced from 14 in four steps in 13.6% overall yield. While the reaction yields of the coupling steps were not optimal at this moment, the rapid assembly of dracaenins A and B in only four steps, in a highly convergent manner and in good overall yields is noteworthy.
Dragon's blood has been highlighted to have the bidirectional regulatory effect of stimulating both blood circulation and coagulation. The active components that could stimulate blood coagulation (hemostatic effect) remain to be discovered. With enough materials synthesized, the effects of dracaenins A and B on adenosine diphosphate (ADP), arachidonic acid (AA) or collagen induced platelet aggregation were evaluated by the light transmission method (Fig. 2). As shown in 1b, ADP (2.5 µmol/L) mediated platelet aggregation was obviously stimulated by dracaenin B in a concentration-dependent manner, with average increasing rates of 8.02%, 9.15%, 13.87%, 19.76% and 114.18% at concentrations of 0.98, 2.9, 8.8, 26.3 and 79 µmol/L, respectively. Dracaenin B also showed marked stimulating effects in a concentration dependent manner with the increasing rates of 7.17%, 12.71%, 28.52%, 35.94% and 51.29% on collagen induced platelet aggregation, and 0.24%, 1.10%, 2.22%, 43.95% and 71.04% increasing rates on AA induced platelet aggregation at concentration range from 0.98 µmol/L to 79 µmol/L (2b and 3b). The stimulating effect on platelet aggregation was also observed using dracaenin A (1a-3a), albeit less potent than that of dracaenin B. These results revealed the effects of dracaenins A and B in stimulating platelet aggregation, and shed light on the possible origin of the hemostatic effect of dragon's blood.
In conclusion, dracaenins A and B represent the unusual chalcane-anthocyanidin dimers isolated from dragon's blood. We have achieved the first total synthesis of these natural products in only 4 steps. Our synthesis features the convergent coupling of three readily available fragments with minimized reliance on protecting groups. The chemical synthesis enables the discovery of their activity in stimulating platelet aggregation, and thus, sheds light on the possible origin of the hemostatic effect of dragon's blood.
Declaration of competing interest
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The authors declare no conflict of interest.
Acknowledgments
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This work was supported by the National Natural Science Foundation of China (No. 21871161), Key Project at Central Government Level for the Ability Establishment of Sustainable Use for Valuable Chinese Medicine Resources (No. 2060302) and Postgraduate Research & Practice Innovation Program of Jiangsu Province (No. KYCX19_1256).
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2021.10.067
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Appendix
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Year 2022 volume 33 Issue 5
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Article Info
doi: 10.1016/j.cclet.2021.10.067
  • Receive Date：2021-09-03
  • Online Date：2025-12-19
  • Published：2022-05-15
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History
  • Received：2021-09-03
  • Revised：2021-10-21
  • Accepted：2021-10-22
Affiliations
    aCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China
    bSchool of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China
    cState Key Laboratory Breeding Base of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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