Stigmasteryl glucoside (BioDeep_00000017385)

 

Secondary id: BioDeep_00000411469

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

化学式: C35H58O6 (574.4233)
中文名称: 豆甾醇葡萄糖苷, 豆甾醇葡萄糖甙, STIGMASTEROL GLUCOSIDE
谱图信息: 最多检出来源 Homo sapiens(otcml) 4.35%

分子结构信息

SMILES: C1[C@@H](CC2=CC[C@@H]3[C@@H]([C@]2(C1)C)CC[C@]1([C@H]3CC[C@@H]1[C@H](C)/C=C/[C@H](C(C)C)CC)C)O[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO
InChI: InChI=1S/C35H58O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h8-10,20-22,24-33,36-39H,7,11-19H2,1-6H3/b9-8+/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1

描述信息

Stigmasterol 3-O-beta-D-glucoside is a steroid saponin that is (3beta,22E)-stigmasta-5,22-dien-3-ol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It is isolated from Symplocos lancifolia. It has a role as a metabolite. It is a member of phytosterols, a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a stigmasterol. It derives from a hydride of a stigmastane.
Stigmasterol glucoside is a natural product found in Ficus virens, Annona purpurea, and other organisms with data available.
A steroid saponin that is (3beta,22E)-stigmasta-5,22-dien-3-ol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It is isolated from Symplocos lancifolia.
Isolated from soya bean oil (Glycine max). Stigmasteryl glucoside is found in fats and oils, pulses, and cloves.
Stigmasteryl glucoside is found in cloves. Stigmasteryl glucoside is isolated from soya bean oil (Glycine max

同义名列表

52 个代谢物同义名

(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (2R,3R,4S,5S,6R)-2-{[(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,3E,5S)-5-ethyl-6-methylhept-3-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol; (3beta,22E)-stigmasta-5,22-dien-3-yl beta-D-glucopyranoside; 3-O-(beta-D-glucopyranosyl)-stigmast-5,22E-dien-3beta-ol; (3β,22E)-Stigmasta-5,22-dien-3-yl β-D-glucopyranoside; (3beta)-stigmast-5,22E-dien-3-yl D-glucopyranoside; Stigmasta-5,22-dien-3-O-.beta.-D-glucopyranoside; Stigmasta-5,22-diene-3-O-beta-D-glucopyranoside; delta5-Stigmasterol 3-O-beta-D-glucopyranoside; beta-Stigmasteryl 3-O-beta-D-glucopyranoside; Stigmasta-5,22-diene-3-O-β-D-glucopyranoside; 3-O-beta-D-Glucopyranosyl-beta-stigmasterol; stigma-5,22-dien-3-beta-D-glucopyranoside; Stigmasterol-3-O-beta-D-glucopyranoside; stigmasterol 3-O-beta-D-glucopyranoside; Stigmasteryl-3-O-beta-D-glucopyranoside; Δ5-Stigmasterol 3-O-β-D-glucopyranoside; Stigma-5,22-dien-3-β-D-glucopyranoside; β-Stigmasteryl 3-O-β-D-glucopyranoside; 3-O-β-D-Glucopyranosyl-β-stigmasterol; Stigmasterol 3-beta-D-glucopyranoside; 3-O-beta-D-glucopyranosylstigmasterol; Stigmasterol beta-D-glucopyranoside; Stigmasteryl beta-D-glucopyranoside; 3-O-β-D-Glucopyranosylstigmasterol; Stigmasterol 3-β-D-glucopyranoside; Stigmasterol beta-glucopyranoside; stigmasterol 3-O-beta-D-glucoside; Stigmasterol β-D-glucopyranoside; Stigmasteryl β-D-glucopyranoside; Stigmasterol 3-beta-D-glucoside; stigmasteryl 3-beta-D-glucoside; Stigmasterol β-glucopyranoside; Stigmasterol 3-O-b-D-glucoside; Stigmasterol 3-O-β-D-glucoside; Stigmasteryl beta-D-glucoside; Stigmasterol beta-D-glucoside; Stigmasterol-beta-D-glucoside; Stigmasteryl 3-b-D-glucoside; Stigmasterol 3-β-D-glucoside; Stigmasteryl 3-β-D-glucoside; Stigmasterol 3-b-D-glucoside; Stigmasteryl beta-glucoside; Stigmasterol β-D-glucoside; Stigmasterol 3-O-glucoside; Stigmasterol O-glucoside; Stigmasteryl D-glucoside; Stigmasteryl β-glucoside; Stigmasteryl glucoside; Stigmasterol glucoside; ST 29:2;O;Hex



数据库引用编号

13 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

0 个相关的代谢反应过程信息。

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BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

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143 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表


文献列表

  • Trang T T Nguyen, Ha V H Nguyen. Effects of Fermentation Conditions Using Lactobacillus plantarum on the Charantin, Stigmasterol Glucoside and β-sitosterol Glucoside Contents of Bitter Gourd (Momordica charantia L.) Juice. Plant foods for human nutrition (Dordrecht, Netherlands). 2020 Dec; 75(4):656-658. doi: 10.1007/s11130-020-00860-w. [PMID: 33009632]
  • Niranjan Das, Abhijit Bhattacharya, Sudip Kumar Mandal, Utsab Debnath, Biswanath Dinda, Subhash C Mandal, Prabir Kumar Sinhamahapatra, Amresh Kumar, M Dutta Choudhury, Sabyasachi Maiti, Partha Palit. Ichnocarpus frutescens (L.) R. Br. root derived phyto-steroids defends inflammation and algesia by pulling down the pro-inflammatory and nociceptive pain mediators: An in-vitro and in-vivo appraisal. Steroids. 2018 11; 139(?):18-27. doi: 10.1016/j.steroids.2018.09.005. [PMID: 30217788]
  • Lynda Golea, Mohammed Benkhaled, Catherine Lavaud, Christophe Long, Hamada Haba. Phytochemical components and biological activities of Silene arenarioides Desf. Natural product research. 2017 Dec; 31(23):2801-2805. doi: 10.1080/14786419.2017.1294174. [PMID: 28278644]
  • Dongping Liu, Guiping Kong, Quan Cheng Chen, Guanghui Wang, Jie Li, Yang Xu, Ting lin, Yingpu Tian, Xiaokun Zhang, Xinsheng Yao, Gensheng Feng, Zhongxian Lu, Haifeng Chen. Fatty acids as natural specific inhibitors of the proto-oncogenic protein Shp2. Bioorganic & medicinal chemistry letters. 2011 Nov; 21(22):6833-7. doi: 10.1016/j.bmcl.2011.09.023. [PMID: 21962577]
  • Vichai Reutrakul, Natthinee Anantachoke, Manat Pohmakotr, Thaworn Jaipetch, Chalobon Yoosook, Jittra Kasisit, Chanita Napaswa, Ampai Panthong, Thawatchai Santisuk, Samran Prabpai, Palangpon Kongsaeree, Patoomratana Tuchinda. Anti-HIV-1 and anti-inflammatory lupanes from the leaves, twigs, and resin of Garcinia hanburyi. Planta medica. 2010 Mar; 76(4):368-71. doi: 10.1055/s-0029-1186193. [PMID: 19830655]
  • Elfita Elfita, Muharni Muharni, Madyawati Latief, Darwati Darwati, Ari Widiyantoro, Supriyatna Supriyatna, Husein H Bahti, Dachriyanus Dachriyanus, Paul Cos, Louis Maes, Kenne Foubert, Sandra Apers, Luc Pieters. Antiplasmodial and other constituents from four Indonesian Garcinia spp. Phytochemistry. 2009 May; 70(7):907-12. doi: 10.1016/j.phytochem.2009.04.024. [PMID: 19481231]
  • Han-shen Zhen, Xue-yan Zhu, Ru-mei Lu, Jie Liang, Qin Qiu, Qi-miao Meng. [Research on chemical constituents from stem of Gymnema sylvestre]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2008 Aug; 31(8):1154-6. doi: ". [PMID: 19112892]
  • Laxminarain Misra, Priyanka Mishra, Archana Pandey, Rajender S Sangwan, Neelam S Sangwan, Rakesh Tuli. Withanolides from Withania somnifera roots. Phytochemistry. 2008 Feb; 69(4):1000-4. doi: 10.1016/j.phytochem.2007.10.024. [PMID: 18061221]
  • Guiyan Liu, Jian Zheng, Zhenxi Yu, Ji Zhang, Ruichao Lin. [Study on sterols and triterpenes from the stems of Akebia quinata]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2005 Dec; 28(12):1060-2. doi: ". [PMID: 16568660]
  • Maria-Teresa Gutierrez-Lugo, Yuehong Wang, Scott G Franzblau, Enrique Suarez, Barbara N Timmermann. Antitubercular sterols from Thalia multiflora Horkel ex Koernicke. Phytotherapy research : PTR. 2005 Oct; 19(10):876-80. doi: 10.1002/ptr.1731. [PMID: 16261518]
  • Sabrina Dallavalle, Lalith Jayasinghe, B M M Kumarihamy, Lucio Merlini, Loana Musso, Leonardo Scaglioni. A new 3,4-seco-lupane derivative from Lasianthus gardneri. Journal of natural products. 2004 May; 67(5):911-3. doi: 10.1021/np030374g. [PMID: 15165165]
  • Esperanza J Carcache-Blanco, Young-Hwa Kang, Eun Jung Park, Bao-Ning Su, Leonardus B S Kardono, Soedarsono Riswan, Harry H S Fong, John M Pezzuto, A Douglas Kinghorn. Constituents of the stem bark of Pongamia pinnata with the potential to induce quinone reductase. Journal of natural products. 2003 Sep; 66(9):1197-202. doi: 10.1021/np030207g. [PMID: 14510596]
  • Wenyi Kang, Xiaojiang Hao, Guohong Li. [Study on the constituents from Neonauclea sessilifolia]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2002 Dec; 25(12):875-7. doi: ". [PMID: 12685347]
  • I Khabazian, J S Bains, D E Williams, J Cheung, J M B Wilson, B A Pasqualotto, S L Pelech, R J Andersen, Y-T Wang, L Liu, A Nagai, S U Kim, U-K Craig, C A Shaw. Isolation of various forms of sterol beta-D-glucoside from the seed of Cycas circinalis: neurotoxicity and implications for ALS-parkinsonism dementia complex. Journal of neurochemistry. 2002 Aug; 82(3):516-28. doi: 10.1046/j.1471-4159.2002.00976.x. [PMID: 12153476]