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引用本文的文献
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Tigliane and daphnane diterpenoids from Thymelaeaceae family: chemistry, biological activity, and potential in drug discovery.瑞香科和铁青树科的二萜类化合物：化学、生物活性及在药物发现中的潜力。
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本文引用的文献
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LC-MS Identification, Isolation, and Structural Elucidation of Anti-HIV Tigliane Diterpenoids from .来自……的抗HIV大戟烷二萜类化合物的液相色谱-质谱联用鉴定、分离及结构解析
J Nat Prod. 2021 Aug 27;84(8):2366-2373. doi: 10.1021/acs.jnatprod.1c00570. Epub 2021 Aug 17.
2
New phorbol ester derivatives as potent anti-HIV agents.新型佛波酯衍生物作为有效的抗 HIV 药物。
Bioorg Med Chem Lett. 2021 Oct 15;50:128319. doi: 10.1016/j.bmcl.2021.128319. Epub 2021 Aug 14.
3
Anti-HIV Tigliane Diterpenoids from .从. 中分离得到的抗 HIV 雷公藤二萜。
J Nat Prod. 2020 Dec 24;83(12):3584-3590. doi: 10.1021/acs.jnatprod.0c00700. Epub 2020 Nov 10.
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Phase I dose-escalation study to determine the safety, tolerability, preliminary efficacy and pharmacokinetics of an intratumoral injection of tigilanol tiglate (EBC-46).一项评估 EBC-46（替拉诺他）瘤内注射的安全性、耐受性、初步疗效和药代动力学的 I 期剂量递增研究。
EBioMedicine. 2019 Dec;50:433-441. doi: 10.1016/j.ebiom.2019.11.037. Epub 2019 Dec 3.
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Tigliane diterpenoids from the Euphorbiaceae and Thymelaeaceae families.来自大戟科和瑞香科的大戟烷二萜类化合物。
Chem Rev. 2015 May 13;115(9):2975-3011. doi: 10.1021/cr200397n. Epub 2015 Apr 23.
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Highly potent, synthetically accessible prostratin analogs induce latent HIV expression in vitro and ex vivo.高效能、可合成获得的普瑞巴林类似物在体外和离体诱导潜伏 HIV 表达。
Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11698-703. doi: 10.1073/pnas.1302634110. Epub 2013 Jun 28.
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Picomolar dichotomous activity of gnidimacrin against HIV-1.对 HIV-1 具有皮摩尔二项式活性的 gnidimacrin。
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Stelleralides A-C, novel potent anti-HIV daphnane-type diterpenoids from Stellera chamaejasme L.瑞香狼毒中的新型强效抗 HIV 瑞香烷型二萜化合物：Stelleralides A-C
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Practical synthesis of prostratin, DPP, and their analogs, adjuvant leads against latent HIV.前体素、二肽基肽酶（DPP）及其类似物的实用合成，针对潜伏性HIV的辅助先导化合物。
Science. 2008 May 2;320(5876):649-52. doi: 10.1126/science.1154690.
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Synthesis of new phorbol derivatives having ethereal side chain and evaluation of their anti-HIV activity.具有醚侧链的新型佛波醇衍生物的合成及其抗HIV活性评估。
Bioorg Med Chem. 2005 Jul 15;13(14):4383-8. doi: 10.1016/j.bmc.2005.04.056.
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