4-demethyl- (BioDeep_00000396069)
Secondary id: BioDeep_00000008153, BioDeep_00000410596
PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C21H20O7 (384.120897)
中文名称: 4′-去甲基鬼臼毒素
谱图信息:
最多检出来源 Viridiplantae(plant) 0.09%
分子结构信息
SMILES: c12c(cc3c(c1)OCO3)C[C@@H]1[C@@H]([C@@H]2c2cc(c(c(c2)OC)O)OC)C(=O)OC1
InChI: InChI=1S/C21H20O7/c1-24-16-5-11(6-17(25-2)20(16)22)18-13-7-15-14(27-9-28-15)4-10(13)3-12-8-26-21(23)19(12)18/h4-7,12,18-19,22H,3,8-9H2,1-2H3/t12-,18+,19-/m0/s1
描述信息
4-demethyldeoxypodophyllotoxin is a member of the class of furonaphthodioxoles that is (5R,5aR,8aR)-5,8,8a,9-tetrahydro-2H-furo[3,4:6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one substituted at position 5 by a 4-hydroxy-3,5-dimethoxyphenyl group. It has a role as a plant metabolite, an immunosuppressive agent, an antioxidant and an antineoplastic agent. It is a lignan, a gamma-lactone, a furonaphthodioxole, a member of methoxybenzenes and a member of phenols.
4-Demethyldeoxypodophyllotoxin is a natural product found in Diphylleia grayi, Hebecarpa macradenia, and other organisms with data available.
A member of the class of furonaphthodioxoles that is (5R,5aR,8aR)-5,8,8a,9-tetrahydro-2H-furo[3,4:6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one substituted at position 5 by a 4-hydroxy-3,5-dimethoxyphenyl group.
同义名列表
17 个代谢物同义名
Furo(3,4:6,7)naphtho(2,3-d)-1,3-dioxol-6(5ah)-one, 5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-, (5R-(5-alpha,5a-beta,8a-alpha))-; (5r,5ar,8ar)-5-(4-hydroxy-3,5-dimethoxy-phenyl)-5,8,8a,9-tetrahydro-5ah-furo[3,4:6,7]naphtho[2,3-d][1,3]dioxol-6-one, AldrichCPR; (10R,11R,15R)-10-(4-hydroxy-3,5-dimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.03,7.011,15]hexadeca-1,3(7),8-trien-12-one; (5R,5aR,8aR)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydro-2H-furo[3,4:6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one; (5R,5aR,8aR)-5-(4-Hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3,4:6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one; (5R,5aR,8aR)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one; Podophyllotoxin, 4-O-demethyl-4-deoxy-; 7-Dehydroxy-4-demethylpodophyllotoxin; (-)-4-desmethyl-deoxypodophyllotoxin; (-)-4-demethyl-deoxypodophyllotoxin; (-)-4-demethyldeoxypodophyllotoxin; 4-desmethyldesoxypodophyllotoxin; 4-demethyldesoxypodophyllotoxin; 4-Demethyl-Deoxypodophyllotoxin; 4-Demethyldeoxypodophyllotoxin; 4-demethyl-; 4'-Demethyldeoxypodophyllotoxin
数据库引用编号
14 个数据库交叉引用编号
- ChEBI: CHEBI:1729
- KEGG: C10552
- PubChem: 160705
- ChEMBL: CHEMBL89905
- MeSH: 4-demethyldesoxypodophyllotoxin
- ChemIDplus: 0003590930
- KNApSAcK: C00002594
- CAS: 3590-93-0
- medchemexpress: HY-N10829
- MetaboLights: MTBLC1729
- PubChem: 12735
- 3DMET: B03950
- NIKKAJI: J15.139D
- KNApSAcK: 1729
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)
BioCyc(1)
- (-)-4'-demethyl-epipodophyllotoxin biosynthesis:
(-)-deoxypodophyllotoxin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ (-)-4'-demethyl-deoxypodophyllotoxin + H2O + MeOH + an oxidized [NADPH-hemoprotein reductase]
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(1)
- (-)-4'-demethyl-epipodophyllotoxin biosynthesis:
(-)-deoxypodophyllotoxin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ (-)-4'-demethyl-deoxypodophyllotoxin + H2O + MeOH + an oxidized [NADPH-hemoprotein reductase]
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 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。
文献列表
- Warren Lau, Elizabeth S Sattely. Six enzymes from mayapple that complete the biosynthetic pathway to the etoposide aglycone.
Science (New York, N.Y.).
2015 Sep; 349(6253):1224-8. doi:
10.1126/science.aac7202
. [PMID: 26359402] - Yan-Jun Sun, Zhan-Lin Li, Hong Chen, Xiao-Qiu Liu, Wei Zhou, Hui-Ming Hua. Three new cytotoxic aryltetralin lignans from Sinopodophyllum emodi.
Bioorganic & medicinal chemistry letters.
2011 Jun; 21(12):3794-7. doi:
10.1016/j.bmcl.2011.04.036
. [PMID: 21570846] - Ren-Wang Jiang, Jin-Rong Zhou, Po-Ming Hon, Song-Lin Li, Yan Zhou, Ling-Lin Li, Wen-Cai Ye, Hong-Xi Xu, Pang-Chui Shaw, Paul Pui-Hay But. Lignans from Dysosma versipellis with inhibitory effects on prostate cancer cell lines.
Journal of natural products.
2007 Feb; 70(2):283-6. doi:
10.1021/np060430o
. [PMID: 17256902] - Aranya Jutiviboonsuk, Hongjie Zhang, Ghee Teng Tan, Cuiying Ma, Nguyen Van Hung, Nguyen Manh Cuong, Nuntavan Bunyapraphatsara, D Doel Soejarto, Harry H S Fong. Bioactive constituents from roots of Bursera tonkinensis.
Phytochemistry.
2005 Dec; 66(23):2745-51. doi:
10.1016/j.phytochem.2005.09.025
. [PMID: 16289147] - M Novelo, J G Cruz, L Hernández, R Pereda-Miranda, H Chai, W Mar, J M Pezzuto. Cytotoxic constituents from Hyptis verticillata.
Journal of natural products.
1993 Oct; 56(10):1728-36. doi:
10.1021/np50100a011
. [PMID: 8277312]