CAS: 126-18-1; (2Ar,4S,5'R,6As,6Bs,8As,8Br,9S,10R,11As,12As,12Br)-5',6A,8A,9-Tetramethyldocosahydrospiro[naphtho[2',1':4,5]Indeno[2,1-B]Furan-10,2'-Pyran]-4-Ol

该化合物是自然产生的一种来自各种植物来源,特别是人造螺旋体的血清素,其特征是其血清结构,其中包括一个典型的多种沙邦氏菌的精密环球热血杆菌核.Smilagenin展示了一系列生物活动,包括抗炎,抗氧化剂和潜在的免疫诱导作用,这使它对药理学研究感兴趣.其溶性特性受其遗传性的影响,这可能影响其生物利用率和与生物膜的相互作用.此外,Smilagenin还就其潜在的治疗应用进行了研究,特别是在传统医学中,它常常与增强活力和总体健康有关.该化合物的安全性特征和功效是正在进行的研究的主题,许多自然产品都是常见的.

结构式图片

MSDS等安全信息

上下游产品

(25R)-5β-spirostan-3-one (25R)-spirost-4-ene-3-one diosgenin sarsasapogenin(25R)-5β-spirostan-3α-ol acetate O-(toluene-4-sulfonyl)-epismilageninO-(toluene-4-sulfonyl)-epismilagenin smilagenin acetate O-Benzoyl-smilageninO-Benzoyl-smilagenin

合成工艺路线路线简述

    📜(25R)-螺甾-4-烯-3-酮置于sodium Tetrahydroborate,5%-Palladium/activated Carbon,氢气体系中,用 四氢呋喃,甲醇 用作溶剂,化学反应 4.0H,反应生成菝葜
    参考文献:薯蓣皂苷元衍生物,其药物组合物及其应用
    标题:薯蓣皂苷元衍生物,其药物组合物及其应用
    摘要:本发明涉及一种薯蓣皂苷元衍生物,所述的薯蓣皂苷元衍生物的结构式如通式(1)所示,本发明还提供了上述薯蓣皂苷元衍生物的药物组合物及其应用,首次对该先导化合物进行了系统性的针对3位和5/6位双键进行结构修饰,合成了一系列新化合物,这些新化合物通过相关靶点的活性测试,很多显示出优于先导化合物的活性,对于治疗神经退行性疾病十分有价值.弥补了现有技术中薯蓣皂苷元衍生物的不足,十分有意义.

    海关参考信息

    专利信息


    专利号:EP-1172094-B1
    优先权日:2000-07-13
    标题:Composition, particularly for cosmetics, comprising DHEA and/or precursor or derivative, and at least a compound which increases the synthesis of glycosaminoglycans
    发明人:ALLEC JOSIANE; CLEREN NATHALIE
    权利人:OREAL
    摘要:Cosmetic composition comprises: (a) dehydroepiandrosterone (DHEA) and/or a DHEA precursor or derivative; and (b) a compound that promotes glycosaminoglycan synthesis or a natural extract containing such a compound.

    专利号:UA-81133-C2
    优先权日:2002-10-28
    标 题 :Process of stereospecific synthesis of 3-hydroxy-5?-h steroidal sapogenins, process of conversion and processes for the preparation of smilagenin and epismilagenin

    专利号:EP-3002290-B1
    优先权日:2007-06-19
    标 题:Synthesis of deoxycholic acid (dca)
    发明人:MORIARTY ROBERT M; DAVID NATHANIEL E; MAHMOOD NADIR AHMEDUDDIN; PRASAD ACHAMPETA RATHAN; SWARINGEN ROY A JR; REID JOHN GREGORY; SAHOO AKHILA KUMAR
    权利人:ALLERGAN SALES LLC

    专利号:US-11427476-B2
    优先权日:2016-04-22
    标题:Mesoporous silicas and method for the synthesis thereof
    发明人:CROIZET-BERGER Karine; DELMEULE Maxime; ESTAGER JULIEN; MANNU NICOLAS; KARTHEUSER BENOIT
    权利人:SILINNOV S C R L
    摘要:The present invention provides a mesoporous silica comprising of components A and B such that component A is a surfactant of a saponin family and component B is a precursor of a silica. The present inventions also provides a method of producing said mesoporous silica by mixing components A and B in a solvent.

    专利号:EP-3002290-A2
    优先权日:2007-06-19
    标 题 :Synthesis of deoxycholic acid (dca)

    专利号:US-9751877-B2
    优先权日:2012-09-21
    标题 :Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders
    发明人:PETTERSSON MARTIN YOUNGJIN; JOHNSON DOUGLAS SCOTT; SUBRAMANYAM CHAKRAPANI; O'DONNELL CHRISTOPHER JOHN; AM ENDE CHRISTOPHER WILLIAM; GREEN MICHAEL ERIC; PATEL NANDINI CHATURBHAI; STIFF CORY MICHAEL; TRAN TUAN PHONG; KAUFFMAN GREGORY WAYNE; STEPAN ANTONIA FRIEDERIKE; VERHOEST PATRICK ROBERT
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Alotaibi MO, Alotaibi NM, Alwaili MA, Alshammari N, Adnan M, Patel M. Natural sapogenins as potential inhibitors of aquaporins for targeted cancer therapy: computational insights into binding and inhibition mechanism. J Biomol Struct Dyn. 2024 Jan
    4:1-22. doi: 10.1080/07391102.2023.2299743. Epub ahead of print. 318(Pt B):117012. doi: 10.1016/j.jep.2023.117012. Epub 2023 Aug 9.
    118:154956. doi: 10.1016/j.phymed.2023.154956. Epub 2023 Jul 17. 27(8):3681-3698. doi: 10.26355/eurrev_202304_32165. 26(7):2024. doi: 10.3390/molecules26072024.

    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    参考文献:10.1007/bf01898451
    摘要:Mitsuyasu N, Izumiya N. Synthesis of a cyclic decapeptide corresponding to tyrocidine E. Cellular and Molecular Life Sciences. 1970 May;26(5):476–7. doi: 10.1007/bf01898451.
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