CAS: 465-00-9; (4As,6As,6Br,8Ar,9R,10R,11R,12Ar,12Br,14Bs)-10,11-Dihydroxy-9-(Hydroxymethyl)-2,2,6A,6B,9,12A-Hexamethyl-1,3,4,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-Octadecahydropicene-4A(2H)-Carboxylic Acid

该化合物是一种自然产生的单环三叶类化合物,主要产自甲状腺的树皮,它具有显著的生物活动,包括抗氧化剂,抗炎和肝脏保护特性.其化学结构的特点是乳腺骨骼,它有助于它研究自由基和调节细胞信号路径的能力.亚氨酸在减轻氧化性压力,糖尿病和心血管障碍方面的潜在治疗应用得到了广泛研究.其高纯度和稳定性使其适合于药物学和营养学研究.该化合物通常通过染色术孤立,确保科学和工业用途的质量.

结构式图片

上下游产品

CAS号22452-82-0 2α,3β,23-Trihyd... | CAS号60393-75-1 (4aS,6aS,6bR,8a... | CAS号60393-73-9 (4aS,6aS,6bR,8a...

合成工艺路线路线简述

    Asteryunnanoside A置于盐酸体系中,化学反应 4.0H,以35 Mg的收率获得产物阿江榄仁酸
    参考文献:Triterpene Saponins From Aster Yunnanensis
    标题:Triterpene Saponins From Aster Yunnanensis
    摘要:Four New Triterpene Saponins,Asteryunnanosides A,B,C And D,Have Been Isolated From Aster Yunnanensis And Their Structures Deduced As 2 Alpha,3 Beta,23-Trihydroxyolean-12-En-28-Oic Acid-28-O-Alpha-L-Rhamnopyranosyl-(1--> 2)-Beta-D-Glucopyranoside,2 Alpha,3 Beta,23-Trihydroxyolean-12-En-28-Oic Acid-28-O-Beta-D-Glucopyranosyl-(1--> 2)-Beta-D-Glucopyranoside,2 Alpha,3 Beta-Dihydroxyolean-12-En-28-Oic Acid-28-O-Alpha-L-Rhamnopyranosyl-(1--> 2)-Beta-D-Glucopyranoside And 2 Alpha,3 Beta-Dihydroxyolean-12-En-28-Oic Acid-28-O-Beta-D-Glucopyranosyl-(1--> 2)-Beta-D-Glucopyranoside,Respectively,By Means Of Spectral And Chemical Data.
    DOI:10.1016/0031-9422(94)00794-T

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    CAS号:465-00-9
    中文名:阿江榄仁酸
    英文名:Arjunolic acid
    纯度:99% HPLC1G/5G/1KG
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    主要参考文献


    1: Dawé A, Mbiantcha M, Yakai F, Jabeen A, Ali MS, Lateef M, Ngadjui BT. Flavonoids and triterpenes from Combretum fragrans with anti-inflammatory, antioxidant and antidiabetic potential. Z Naturforsch C. 2018 Apr 25;73(5-6):211-219. doi: 10.1515/znc-2017-0166. doi: 10.1186/s12906-017-1935-5.
    3: Bansal T, Chatterjee E, Singh J, Ray A, Kundu B, Thankamani V, Sengupta S, Sarkar S. Arjunolic acid, a peroxisome proliferator-activated receptor α agonist, regresses cardiac fibrosis by inhibiting non-canonical TGF-β signaling. J Biol Chem. 2017 Oct 6;292(40):16440-16462. doi: 10.1074/jbc.M117.788299. Epub 2017 Aug 18.
    4: Maity M, Perveen H, Dash M, Jana S, Khatun S, Dey A, Mandal AK, Chattopadhyay S. Arjunolic Acid Improves the Serum Level of Vitamin B(12) and Folate in the Process of the Attenuation of Arsenic Induced Uterine Oxidative Stress. Biol Trace Elem Res. 2018 Mar;182(1):78-90. doi: 10.1007/s12011-017-1077-0. Epub 2017 Jun 28. doi: 10.1002/tcr.201600123. Epub 2017 Feb 14. Review. doi: 10.1016/j.phymed.2016.08.003. Epub 2016 Aug 17. doi: 10.1080/14786419.2016.1241998. Epub 2016 Oct 13. doi: 10.1002/asia.201600773. Epub 2016 Aug 11. doi: 10.1016/j.biopha.2016.04.046. Epub 2016 May 3. doi: 10.1016/j.jep.2016.07.061. Epub 2016 Jul 25. Chinese. doi: 10.17179/excli2016-252. eCollection 2016.

    合成参考文献


    参考文献:10.1016/s0031-9422(01)00180-7
    摘要:Gu JQ, Park EJ, Luyengi L, Hawthorne ME, Mehta RG, Farnsworth NR, Pezzuto JM, Kinghorn AD. Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity. Phytochemistry. 2001 Sep;58(1):121–7. doi: 10.1016/s0031-9422(01)00180-7.
    参考文献:10.1248/cpb.54.775
    摘要:Wang D, Xia M, Cui Z. New triterpenoids isolated from the root bark of Ulmus pumila L. Chem Pharm Bull (Tokyo). 2006 Jun;54(6):775–8. doi: 10.1248/cpb.54.775.
    参考文献:10.1016/j.freeradbiomed.2009.11.023
    摘要:Ghosh J, Das J, Manna P, Sil PC. Arjunolic acid, a triterpenoid saponin, prevents acetaminophen (APAP)-induced liver and hepatocyte injury via the inhibition of APAP bioactivation and JNK-mediated mitochondrial protection. Free Radic Biol Med. 2010 Feb 15;48(4):535–53. doi: 10.1016/j.freeradbiomed.2009.11.023.
    参考文献:10.1016/j.phymed.2020.153278
    摘要:Gupta A, Kumar R, Bhattacharyya P, Bishayee A, Pandey AK. Terminalia bellirica (Gaertn.) roxb. (Bahera) in health and disease: A systematic and comprehensive review. Phytomedicine. 2020 Oct;77():153278. doi: 10.1016/j.phymed.2020.153278.
    参考文献:10.1021/np050553t
    摘要:Rudiyansyah, Garson MJ. Secondary Metabolites from the Wood Bark of Durio zibethinus and Durio kutejensis. J. Nat. Prod. 2006 Jul 15;69(8):1218–21. doi: 10.1021/np050553t.
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