Dihydropinosylvin (BioDeep_00000007972)
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C14H14O2 (214.0994)
中文名称: 5-苯乙基-1,3-二羟基苯, 二氢赤松素
谱图信息:
最多检出来源 Viridiplantae(plant) 16.33%
分子结构信息
SMILES: C1=C(O)C=C(CCC2=CC=CC=C2)C=C1O
InChI: InChI=1S/C14H14O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-5,8-10,15-16H,6-7H2
描述信息
Dihydropinosylvin is a member of the class of resorcinols carrying an additional 2-phenylethyl substituent at position 5. It has a role as an EC 1.14.18.1 (tyrosinase) inhibitor and a plant metabolite. It is a member of resorcinols and a diphenylethane.
Dihydropinosylvin is a natural product found in Dioscorea mangenotiana, Stemona tuberosa, and other organisms with data available.
A member of the class of resorcinols carrying an additional 2-phenylethyl substituent at position 5.
Dihydropinosylvin is a stilbenoid that can be found in Stemona collinsae[1].
Dihydropinosylvin is a stilbenoid that can be found in Stemona collinsae[1].
同义名列表
11 个代谢物同义名
5-(2-Phenylethyl)-1,3-benzenediol; 5-Phenethylresorcinol; Dihydropinosylvin; 1,3-Benzenediol, 5-(2-phenylethyl)-; 5-(2-phenylethyl)benzene-1,3-diol; 5-(2-Phenylethyl)-1,3-benzenediol; 5-phenethylbenzene-1,3-diol; 5-(2-phenylethyl)resorcinol; LDBYHULIXFIJAZ-UHFFFAOYSA-N; Resorcinol, 5-phenethyl-; 3,5-Dihydroxybibenzyl; Dihydropinosylvin; Dihydropinosylvin
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:4579
- KEGG: C10254
- PubChem: 442700
- Metlin: METLIN53261
- ChEMBL: CHEMBL228120
- LipidMAPS: LMPK13090034
- MetaCyc: CPD-6963
- KNApSAcK: C00002878
- CAS: 14531-52-3
- medchemexpress: HY-N3753
- PMhub: MS000021497
- MetaboLights: MTBLC4579
- PubChem: 12440
- 3DMET: B03679
- NIKKAJI: J813.419G
- KNApSAcK: 4579
- LOTUS: LTS0256887
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
2 个相关的代谢反应过程信息。
Reactome(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
73 个相关的物种来源信息
- 2 - Bacteria: LTS0256887
- 3805 - Bauhinia: LTS0256887
- 3806 - Bauhinia purpurea: 10.1021/NP070010E
- 3806 - Bauhinia purpurea: LTS0256887
- 24079 - Bignoniaceae: LTS0256887
- 4672 - Dioscorea: LTS0256887
- 55571 - Dioscorea alata:
- 55571 - Dioscorea alata: 10.1016/S0031-9422(00)98053-1
- 55571 - Dioscorea alata: LTS0256887
- 29710 - Dioscorea cayenensis: LTS0256887
- 55577 - Dioscorea cayenensis subsp. rotundata: 10.1016/S0031-9422(00)82467-X
- 55577 - Dioscorea cayenensis subsp. rotundata: LTS0256887
- 4673 - Dioscorea japonica: 10.1016/J.BMCL.2011.02.003
- 4673 - Dioscorea japonica: LTS0256887
- 1640673 - Dioscorea mangenotiana: 10.1021/NP50071A033
- 1640673 - Dioscorea mangenotiana: LTS0256887
- 569628 - Dioscorea oppositifolia:
- 569628 - Dioscorea oppositifolia: 10.1016/S0031-9422(00)81417-X
- 569628 - Dioscorea oppositifolia: LTS0256887
- 55575 - Dioscorea polystachya:
- 55575 - Dioscorea polystachya: 10.1016/S0031-9422(00)81417-X
- 55575 - Dioscorea polystachya: LTS0256887
- 4671 - Dioscoreaceae: LTS0256887
- 2759 - Eukaryota: LTS0256887
- 3803 - Fabaceae: LTS0256887
- 1236 - Gammaproteobacteria: LTS0256887
- 4447 - Liliopsida: LTS0256887
- 3398 - Magnoliopsida: LTS0256887
- 83950 - Oroxylum: LTS0256887
- 83951 - Oroxylum indicum: LTS0256887
- 83951 - Oroxylum indicum: NA
- 3318 - Pinaceae: LTS0256887
- 58019 - Pinopsida: LTS0256887
- 3337 - Pinus: LTS0256887
- 71622 - Pinus albicaulis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71622 - Pinus albicaulis: LTS0256887
- 88733 - Pinus armandii: 10.1016/0031-9422(88)80201-2
- 88733 - Pinus armandii: LTS0256887
- 71625 - Pinus ayacahuite: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71625 - Pinus ayacahuite: LTS0256887
- 3338 - Pinus balfouriana: 10.3891/ACTA.CHEM.SCAND.05-0121
- 3338 - Pinus balfouriana: LTS0256887
- 58041 - Pinus cembra: 10.3891/ACTA.CHEM.SCAND.05-0121
- 58041 - Pinus cembra: LTS0256887
- 151559 - Pinus flexilis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 151559 - Pinus flexilis: LTS0256887
- 71644 - Pinus parviflora: 10.1016/0031-9422(88)80201-2
- 71644 - Pinus parviflora: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71644 - Pinus parviflora: LTS0256887
- 62752 - Pinus sibirica:
- 399189 - Pinus strobiformis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 399189 - Pinus strobiformis: LTS0256887
- 3349 - Pinus sylvestris: 10.1007/BF00040665
- 3349 - Pinus sylvestris: LTS0256887
- 33090 - Plants: -
- 135621 - Pseudomonadaceae: LTS0256887
- 286 - Pseudomonas: LTS0256887
- 36746 - Pseudomonas cichorii: 10.1016/S0031-9422(00)81417-X
- 36746 - Pseudomonas cichorii: LTS0256887
- 85281 - Stemona: LTS0256887
- 2801495 - Stemona pierrei:
- 2801495 - Stemona pierrei: 10.1016/J.PHYTOCHEM.2003.09.015
- 2801495 - Stemona pierrei: 10.1021/NP0497043
- 2801495 - Stemona pierrei: LTS0256887
- 167572 - Stemona tuberosa:
- 167572 - Stemona tuberosa: 10.1021/NP0497043
- 167572 - Stemona tuberosa: LTS0256887
- 167572 - Stemona tuberosa Lour.: -
- 49662 - Stemonaceae: LTS0256887
- 35493 - Streptophyta: LTS0256887
- 58023 - Tracheophyta: LTS0256887
- 33090 - Viridiplantae: LTS0256887
- 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
- Surat Boonphong, Pakawan Puangsombat, Apiwat Baramee, Chulabhorn Mahidol, Somsak Ruchirawat, Prasat Kittakoop. Bioactive compounds from Bauhinia purpurea possessing antimalarial, antimycobacterial, antifungal, anti-inflammatory, and cytotoxic activities.
Journal of natural products.
2007 May; 70(5):795-801. doi:
10.1021/np070010e
. [PMID: 17480099] - Tong Zhang, Ya-Zhong Zhang, Jian-Sheng Tao. Antibacterial constituents from Stemona sessilifolia.
Journal of Asian natural products research.
2007 Apr; 9(3-5):479-85. doi:
10.1080/10286020701189286
. [PMID: 17701569] - 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]