Myricadiol (BioDeep_00000396550)
Main id: BioDeep_00000021560
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C30H50O2 (442.38106)
中文名称: 蒲公英赛-14-烯-3BETA,28-二醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1(C)CC[C@]2(CO)CC=C3[C@@](C)(CC[C@H]4[C@@]3(C)CC[C@H]3C(C)(C)[C@@H](O)CC[C@@]34C)[C@@H]2C1
InChI: InChI=1S/C30H50O2/c1-25(2)16-17-30(19-31)15-10-22-28(6)12-8-20-26(3,4)24(32)11-14-27(20,5)21(28)9-13-29(22,7)23(30)18-25/h10,20-21,23-24,31-32H,8-9,11-19H2,1-7H3
描述信息
(3S,4aR,6aR,6aS,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6a,11,11,14b-heptamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol is a natural product found in Tamarix aphylla, Scaevola spinescens, and other organisms with data available.
See also: Myrica cerifera root bark (part of).
同义名列表
20 个代谢物同义名
8a-(hydroxymethyl)-4,4,6a,11,11,12b,14b-heptamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol; (3beta)-D-Friedoolean-14-ene-3,28-diol; D-Friedoolean-14-ene-3β,28-diol; Myricardiol; Myricadiol; 4A(2H)-PICENEMETHANOL, 1,3,4,5,6B,7,8,8A,9,10,11,12,12A,12B,13,14,14A,14B-OCTADECAHYDRO-10-HYDROXY-2,2,6B,9,9,12A,14A-HEPTAMETHYL-, (4AS-(4A.ALPHA.,6B.ALPHA.,8A.BETA.,10.ALPHA.,12A.ALPHA.,12B.BETA.,14A.BETA.,14B.ALPHA.))-; 4A(2H)-PICENEMETHANOL, 1,3,4,5,6B,7,8,8A,9,10,11,12,12A,12B,13,14,14A,14B-OCTADECAHYDRO-10-HYDROXY-2,2,6B,9,9,12A,14A-HEPTAMETHYL-, (4AS-(4Aalpha,6Balpha,8Abeta,10alpha,12Aalpha,12Bbeta,14Abeta,14Balpha))-; 4A(2H)-PICENEMETHANOL, 1,3,4,5,6B,7,8,8A,9,10,11,12,12A,12B,13,14,14A,14B-OCTADECAHYDRO-10-HYDROXY-2,2,6B,9,9,12A,14A-HEPTAMETHYL-, (4AS,6BR,8AR,10S,12AR,12BR,14AS,14BS)-; (3S,4aR,6aR,6aS,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6a,11,11,14b-heptamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol; D-Friedoolean-14-ene-3,28-diol, (3)-; Taraxer-14-ene-3,28-diol; 27-NOROLEAN-14-ENE-3,28-DIOL, 13-METHYL-, (3.BETA.,13.ALPHA.)-; 27-NOROLEAN-14-ENE-3,28-DIOL, 13-METHYL-, (3beta,13alpha)-; D-FRIEDOOLEAN-14-ENE-3,28-DIOL, (3.BETA.)-; D-Friedoolean-14-ene-3,28-diol, (3beta)-; D-FRIEDOOLEAN-14-ENE-3.BETA.,28-DIOL; D-Friedoolean-14-ene-3beta,28-diol; TARAXER-14-ENE-3.BETA.,28-DIOL; TARAXER-14-ENE-3beta,28-DIOL; UNII-89VO0CMD4F; 89VO0CMD4F
数据库引用编号
8 个数据库交叉引用编号
- PubChem: 4979342
- PubChem: 3084282
- Metlin: METLIN90136
- MeSH: myricadiol
- ChemIDplus: 0017884887
- CAS: 17884-88-7
- medchemexpress: HY-N3227
- LOTUS: LTS0234194
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
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)
33 个相关的物种来源信息
- 4441 - Camellia: LTS0234194
- 4443 - Camellia japonica: 10.1007/BF02534064
- 4443 - Camellia japonica: LTS0234194
- 4305 - Celastraceae: LTS0234194
- 2759 - Eukaryota: LTS0234194
- 16472 - Goodeniaceae: LTS0234194
- 123423 - Gymnosporia: LTS0234194
- 3398 - Magnoliopsida: LTS0234194
- 190583 - Morella: LTS0234194
- 3510 - Morella cerifera: 10.1021/NP960230K
- 3510 - Morella cerifera: 10.1248/CPB.48.1427
- 3510 - Morella cerifera: LTS0234194
- 385008 - Morella nana: 10.3184/030823409X447754
- 385008 - Morella nana: LTS0234194
- 262757 - Morella rubra: 10.1016/S0031-9422(00)81515-0
- 262757 - Morella rubra: 10.1080/14786419.2010.516749
- 262757 - Morella rubra: 10.1248/CPB.50.208
- 262757 - Morella rubra: LTS0234194
- 3509 - Myrica: LTS0234194
- 29739 - Myrica gale: 10.1248/YAKUSHI1947.117.4_211
- 29739 - Myrica gale: LTS0234194
- 26766 - Myricaceae: LTS0234194
- 16480 - Scaevola: LTS0234194
- 197987 - Scaevola spinescens: 10.1055/S-2006-957961
- 197987 - Scaevola spinescens: LTS0234194
- 35493 - Streptophyta: LTS0234194
- 63083 - Tamaricaceae: LTS0234194
- 63084 - Tamarix: LTS0234194
- 189786 - Tamarix aphylla: 10.1016/S0031-9422(00)97580-0
- 189786 - Tamarix aphylla: LTS0234194
- 27065 - Theaceae: LTS0234194
- 58023 - Tracheophyta: LTS0234194
- 33090 - Viridiplantae: LTS0234194
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
- Gazanfar Ahmad, Reyaz Hassan, Neerupma Dhiman, Asif Ali. Assessment of Anti-inflammatory Activity of 3-Acetylmyricadiol in LPSStimulated Raw 264.7 Macrophages.
Combinatorial chemistry & high throughput screening.
2022; 25(1):204-210. doi:
10.2174/1386207324666210319122650
. [PMID: 33745430] - Pan Chen, Zhi-jian Fang, Han-jing Yan, Hong-bo Zhou, Quan-xi Mei. [Study on Chemical Constituents of Petroleum Ether Fraction from Rubus alceaefolius].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2015 Jan; 38(1):93-6. doi:
. [PMID: 26214876]
- Ying Zhang, Yi Yuan, Baosong Cui, Shuai Li. [Study on chemical constituents from ethyl acetate extract of Myricaria bracteata].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2011 Apr; 36(8):1019-23. doi:
. [PMID: 21809576]