Isoarnebin I (BioDeep_00001867517)
Main id: BioDeep_00000000519
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C21H22O6 (370.1416)
中文名称: (β,β-二甲基丙烯酰基)紫草素, β,β-二甲基丙烯酰紫草素
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C
InChI: InChI=1S/C21H22O6/c1-11(2)5-8-17(27-18(25)9-12(3)4)13-10-16(24)19-14(22)6-7-15(23)20(19)21(13)26/h5-7,9-10,17,22-23H,8H2,1-4H3/t17-/m1/s1
描述信息
Beta,beta-Dimethylacrylshikonin is a hydroxy-1,4-naphthoquinone.
beta,beta-Dimethylacrylshikonin is a natural product found in Alkanna cappadocica, Lithospermum erythrorhizon, and other organisms with data available.
β,β-Dimethylacrylshikonin (Isoarnebin I) is a naphthoquinone derivative isolated from Lithospermum erythrorhizon Sieb. et Zucc. , promotes angiogenesis by inducing eNOS, VEGF and HIF-1α expression through the PI3K-dependent pathway.β,β-Dimethylacrylshikonin has anti-tumor activity[1].
β,β-Dimethylacrylshikonin (Isoarnebin I) is a naphthoquinone derivative isolated from Lithospermum erythrorhizon Sieb. et Zucc. , promotes angiogenesis by inducing eNOS, VEGF and HIF-1α expression through the PI3K-dependent pathway.β,β-Dimethylacrylshikonin has anti-tumor activity[1].
β,β-Dimethylacrylshikonin (Isoarnebin I) is a naphthoquinone derivative isolated from Lithospermum erythrorhizon Sieb. et Zucc. , promotes angiogenesis by inducing eNOS, VEGF and HIF-1α expression through the PI3K-dependent pathway.β,β-Dimethylacrylshikonin has anti-tumor activity[1].
同义名列表
17 个代谢物同义名
2-Butenoic acid, 3-methyl-, 1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester, (+)-; 2-Butenoic acid, 3-methyl-, 1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester, (R)-; 2-Butenoic acid, 3-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester; (1R)-1-(5,8-Dihydroxy-1,4-dioxo-1,4-dihydro-2-naphthalenyl)-4-methyl-3-pentenyl 3-methyl-2-butenoate, AldrichCPR; (R)-1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl 3-methylbut-2-enoate; (R)-1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-enyl 3-methylbut-2-enoate; [(1R)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl] 3-methylbut-2-enoate; |A,|A inverted exclamation marka pound-dimethylacrylalkannin; Shikonin beta,beta-dimethylacrylate; (beta,beta-Dimethylacryl)shikonin; beta,beta-Dimethylacrylshikonin; b, b-Dimethylacrylshikonin; β,β-Dimethylacrylshikonin; Dimethylacrylshikonin; dimethylacrylalkannin; Isoarnebin I; beta,beta-Dimethylacrylshikonin
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:81071
- KEGG: C17415
- PubChem: 479499
- ChemIDplus: 0024502792
- CAS: 24502-79-2
- medchemexpress: HY-N5112B
- PubChem: 96023765
- NIKKAJI: J156.605I
- KNApSAcK: 81071
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)
9 个相关的物种来源信息
- 2650392 - Alkanna cappadocica: 10.1021/NP900778J
- 554523 - Alkanna hirsutissima: 10.1080/00021369.1983.10865646
- 373122 - Arnebia euchroma: 10.1055/S-2006-959718
- 373122 - Arnebia euchroma (Royle) Johnst.: -
- 419289 - Arnebia guttata Bunge: -
- 454930 - Jatropha glandulifera: 10.1016/S0031-9422(00)85935-X
- 34254 - Lithospermum erythrorhizon:
- 411250 - Onosma paniculata: 10.1021/NP2006499
- 33090 - Plants: -
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
- Nadine Kretschmer, Beate Rinner, Alexander J A Deutsch, Birgit Lohberger, Heike Knausz, Olaf Kunert, Martina Blunder, Herbert Boechzelt, Helmut Schaider, Rudolf Bauer. Naphthoquinones from Onosma paniculata induce cell-cycle arrest and apoptosis in melanoma Cells.
Journal of natural products.
2012 May; 75(5):865-9. doi:
10.1021/np2006499. [PMID: 22530779] - B Z Ahn, K U Baik, G R Kweon, K Lim, B D Hwang. Acylshikonin analogues: synthesis and inhibition of DNA topoisomerase-I.
Journal of medicinal chemistry.
1995 Mar; 38(6):1044-7. doi:
10.1021/jm00006a025. [PMID: 7699697]
