Batatasin III (BioDeep_00000017433)

human metabolite PANOMIX_OTCML-2023 Endogenous

代谢物信息卡片

1-(3-Hydroxy-5-methoxyphenyl)-2-(3-hydroxyphenyl)ethane

化学式: C15H16O3 (244.1099386)
中文名称: 山药素Ⅲ, 山药素Ⅲ
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 3.17%

分子结构信息

SMILES: c1cc(cc(c1)CCc1cc(cc(c1)O)OC)O
InChI: InChI=1S/C15H16O3/c1-18-15-9-12(8-14(17)10-15)6-5-11-3-2-4-13(16)7-11/h2-4,7-10,16-17H,5-6H2,1H3

描述信息

Batatasin III is a stilbenoid.
batatasin III is a natural product found in Bulbophyllum reptans, Cymbidium aloifolium, and other organisms with data available.
Batatasin III is found in root vegetables. Batatasin III is a constituent of Dioscorea batatas (Chinese yam)
Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1].
Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1].
Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1].

同义名列表

9 个代谢物同义名

1-(3-Hydroxy-5-methoxyphenyl)-2-(3-hydroxyphenyl)ethane; 3-[2-(3-Hydroxyphenyl)ethyl]-5-methoxyphenol, 9CI; Phenol, 3-[2-(3-hydroxyphenyl)ethyl]-5-methoxy-; 3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol; 3,3-dihydroxy-5-methoxybibenzyl; 3-O-Methylbatatasin III; Batatasin III (4); Batatasin III; BatatasinIII

数据库引用编号

10 个数据库交叉引用编号

ChEBI: CHEBI:174263
PubChem: 10466989
HMDB: HMDB0030636
ChEMBL: CHEMBL450788
KNApSAcK: C00015292
foodb: FDB002540
chemspider: 8642400
CAS: 56684-87-8
medchemexpress: HY-122965
PMhub: MS000005668

分类词条

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

59 个相关的物种来源信息

159935 - Anthogonium gracile: 10.1016/0031-9422(89)80273-0
78703 - Arundina graminifolia:
862845 - Bletilla ochracea: 10.1016/J.FITOTE.2018.02.007
78707 - Bletilla striata:
78707 - Bletilla striata (Thunb. ) Reichb.f.: -
78707 - Bletilla Striata (Thunb.Ex A.Murray)Rchb.F.: -
1185423 - Bulbophyllum andersonii:
2487920 - Bulbophyllum fuscopurpureum:
1470449 - Bulbophyllum guttulatum:
2487474 - Bulbophyllum protractum: 10.1016/S0031-9422(96)00402-5
1097178 - Bulbophyllum reptans:
1138424 - Bulbophyllum vaginatum: 10.1016/S0031-9422(96)00387-1
337206 - Calanthe sylvatica: 10.1016/0031-9422(89)80273-0
141721 - Coelogyne barbata: 10.1016/0031-9422(89)80273-0
947907 - Coelogyne corymbosa: 10.1016/0031-9422(89)80273-0
1470452 - Coelogyne elata: 10.1016/0031-9422(89)80273-0
71595 - Coelogyne flaccida:
466244 - Coelogyne nitida: 10.1016/0031-9422(89)80273-0
2487923 - Coelogyne odoratissima: 10.1016/0031-9422(89)80273-0
1350402 - Coelogyne ovalis: 10.1016/S0031-9422(00)85509-0
141735 - Coelogyne stricta: 10.1016/0031-9422(89)80273-0
112603 - Cymbidium aloifolium:
78742 - Cyrtopodium andersonii: 10.1016/J.JEP.2014.05.006
1547852 - Cyrtopodium macrobulbon: 10.1016/J.JEP.2014.05.006
859504 - Dendrobium amoenum:
234050 - Dendrobium amplum: 10.1002/CHIN.200844207
154290 - Dendrobium aphyllum: 10.1016/0031-9422(89)80273-0
179352 - Dendrobium cariniferum: 10.1007/S10600-009-9290-5
154291 - Dendrobium chrysanthum: 10.1016/0031-9422(89)80273-0
161865 - Dendrobium chrysotoxum: 10.1007/S10600-009-9329-7
161866 - Dendrobium densiflorum: 10.1016/0031-9422(89)80273-0
257356 - Dendrobium draconis: 10.1080/10286020.2010.546354
117953 - Dendrobium fimbriatum: 10.1016/J.BMCL.2014.09.052
859510 - Dendrobium herbaceum: 10.1016/0031-9422(89)80273-0
154294 - Dendrobium lituiflorum: 10.1016/0031-9422(89)80273-0
117954 - Dendrobium loddigesii: 10.1248/CPB.58.628
257357 - Dendrobium longicornu: 10.1007/S10600-010-9743-X
142614 - Dendrobium moniliforme: 10.1016/0031-9422(89)80273-0
94219 - Dendrobium nobile:
1508135 - Dendrobium plicatile: 10.1016/0031-9422(96)00270-1
1354206 - Dendrobium rotundatum: 10.1016/0031-9422(92)83480-M
335155 - Dendrobium terminale: 10.1016/0031-9422(89)80273-0
55571 - Dioscorea alata:
35874 - Dioscorea bulbifera: 10.1002/CBDV.201000279
167584 - Dioscorea dumetorum:
569628 - Dioscorea oppositifolia:
55575 - Dioscorea polystachya:
191066 - Empetrum nigrum: 10.1055/S-2006-959382
426896 - Epidendrum rigidum: 10.1021/JF0508044
59324 - Gymnadenia conopsea:
9606 - Homo sapiens: -
142337 - Nidema boothii: 10.1021/NP030303H
180499 - Pholidota chinensis: 10.1002/HLCA.200890228
141750 - Pholidota imbricata: 10.1016/0031-9422(89)80273-0
33090 - Plants: -
141752 - Pleione bulbocodioides: 10.1016/S0031-9422(96)00758-3
217554 - Scaphyglottis livida: 10.1055/S-1999-14056
38195 - Thunia alba: 10.1016/S0031-9422(98)00433-6
569774 - 金线莲: -

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。

文献列表

Li He, Qian Su, Lan Bai, Meifeng Li, Juanru Liu, Xiaomei Liu, Cunyan Zhang, Zhongliang Jiang, Jun He, Jianyou Shi, Shan Huang, Li Guo. Recent research progress on natural small molecule bibenzyls and its derivatives in Dendrobium species. European journal of medicinal chemistry. 2020 Oct; 204(?):112530. doi: 10.1016/j.ejmech.2020.112530. [PMID: 32711292]
Xue-Ming Zhou, Cai-Juan Zheng, Li-She Gan, Guang-Ying Chen, Xiao-Peng Zhang, Xiao-Ping Song, Gao-Nan Li, Chong-Ge Sun. Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile. Journal of natural products. 2016 07; 79(7):1791-7. doi: 10.1021/acs.jnatprod.6b00252. [PMID: 27310249]
Feng-Qing Xu, Fang-Cheng Xu, Bo Hou, Wei-Wei Fan, Cheng-Ting Zi, Yan Li, Fa-Wu Dong, Yu-Qing Liu, Jun Sheng, Zhi-Li Zuo, Jiang-Miao Hu. Cytotoxic bibenzyl dimers from the stems of Dendrobium fimbriatum Hook. Bioorganic & medicinal chemistry letters. 2014 Nov; 24(22):5268-73. doi: 10.1016/j.bmcl.2014.09.052. [PMID: 25316316]
Diana C Rueda, Angela Schöffmann, Maria De Mieri, Melanie Raith, Evelyn A Jähne, Steffen Hering, Matthias Hamburger. Identification of dihydrostilbenes in Pholidota chinensis as a new scaffold for GABAA receptor modulators. Bioorganic & medicinal chemistry. 2014 Feb; 22(4):1276-84. doi: 10.1016/j.bmc.2014.01.008. [PMID: 24462176]
Min Hye Yang, Kee Dong Yoon, Young-Won Chin, Ju Hyun Park, Jinwoong Kim. Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita. Bioorganic & medicinal chemistry. 2009 Apr; 17(7):2689-94. doi: 10.1016/j.bmc.2009.02.057. [PMID: 19303782]
Yanet Hernández-Romero, Juana-Isela Rojas, Rafael Castillo, Alejandra Rojas, Rachel Mata. Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii. Journal of natural products. 2004 Feb; 67(2):160-7. doi: 10.1021/np030303h. [PMID: 14987052]