angelica lactone (BioDeep_00000395839)
Main id: BioDeep_00000033627
PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C5H6O2 (98.0367776)
中文名称: α-当归内酯
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1=CCC(=O)O1
InChI: InChI=1S/C5H6O2/c1-4-2-3-5(6)7-4/h2H,3H2,1H3
描述信息
Alpha-angelica lactone is an angelica lactone and a butenolide. It is functionally related to a but-3-en-4-olide. It is a tautomer of a beta-angelica lactone.
alpha-Angelica lactone is a natural product found in Picea abies, Tamarindus indica, and Arctostaphylos uva-ursi with data available.
α-Angelica lactone is a naturally occurring anticarcinogen and an vinylogous nucleophile. α-Angelica lactone can give the chiral δ-amino γ,γ-disubstituted butenolide carbonyl derivatives and exhibitselectrophilic trapping at the γ-carbon. α-Angelica lactone exerts strong chemoprotective effects by selective enhancement of glutathione-S-thansferase (GST) and UDP-glucononosyltransferase (UGT) detoxification enzymes[1][2][3][4].
α-Angelica lactone is a naturally occurring anticarcinogen and an vinylogous nucleophile. α-Angelica lactone can give the chiral δ-amino γ,γ-disubstituted butenolide carbonyl derivatives and exhibitselectrophilic trapping at the γ-carbon. α-Angelica lactone exerts strong chemoprotective effects by selective enhancement of glutathione-S-thansferase (GST) and UDP-glucononosyltransferase (UGT) detoxification enzymes[1][2][3][4].
同义名列表
54 个代谢物同义名
3-PENTENOIC ACID,4-HYDROXY,LACTONE ALPHA-ANGELICA-LACTONE; .alpha.(.beta.,.gamma. or .DELTA.2)-Angelica lactone; Penten-3-oic acid, 4-hydroxy-, .gamma.-lactone; 3-Pentenoic acid, 4-hydroxy-, .gamma.-lactone; .gamma.-Methyl-.beta.,.gamma.-crotonolactone; 5-17-09-00120 (Beilstein Handbook Reference); alpha-Angelica lactone, analytical standard; InChI=1/C5H6O2/c1-4-2-3-5(6)7-4/h2H,3H2,1H; 4-Hydroxy-3-pentenoic acid .gamma.-lactone; 4-HYDROXY-3-PENTENOIC ACID.GAMMA.-LACTONE; 4-Hydroxy-3-pentenoic acid gamma-lactone; a-Angelica lactone, =90\\% sum of isomers; gamma-Methyl-beta,gamma-crotonolactone; 4-Hydroxy-3-pentenoic acid ?-lactone; ANGELICA LACTONE .ALPHA.-FORM [MI]; 4-Hydroxypent-3-enoic acid lactone; 3-Pentenoic acid, .gamma.-lactone; angelica lactone, (alpha)-isomer; PENTEN-3-OIC ACID, GAMMA-LACTONE; alpha-Angelica lactone, 98\\%, FG; .beta.,.gamma.-Angelica lactone; .ALPHA.-ANGELICA LACTONE [FHFI]; 2,3-DIHYDRO-5-METHYLFURAN-2-ONE; angelica lactone, (beta)-isomer; 2-Oxo-5-methyl-2,3-dihydrofuran; 5-methyl-2,3-dihydrofuran-2-one; 5-METHYL-2,3-DIHYDRO-2-FURANONE; alpha-Angelica lactone, 98\\%; beta,gamma-Angelica lactone; .delta.(2)-Angelica lactone; delta(2)-Angelica lactone; .DELTA.2-Angelica lactone; 2(3H)-FURANONE, 5-METHYL-; .alpha.-Angelica lactone; .GAMMA.-ANGELICA LACTONE; .alpha.-angelicalactone; 5-Methylfuran-2(3H)-one; alpha -Angelica lactone; 5-methyl-3H-furan-2-one; 5-Methyl-2(3H)-furanone; 4-Methyl-2(3H)-furanone; alpha-Angelica lactone; alpha-angelicalactone; alpha-Angelicalacton; α-Angelica lactone; PENT-3-EN-4-OLIDE; a-Angelic lactone; WLN: T5OV CHJ E1; angelica lactone; UNII-29CRF6L9C5; Tox21_303997; 29CRF6L9C5; AI3-04326; alpha-Angelica lactone
数据库引用编号
7 个数据库交叉引用编号
- ChEBI: CHEBI:36433
- PubChem: 11559
- ChEMBL: CHEMBL478640
- MeSH: angelica lactone
- ChemIDplus: 0000591128
- CAS: 591-12-8
- medchemexpress: HY-N0548
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)
2 个相关的物种来源信息
- 33090 - Plants: -
- 58860 - Tamarindus indica: 10.1080/10412905.1990.9697860
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
- Gerlinde Scharf, Sonja Prustomersky, Siegfried Knasmuller, Rolf Schulte-Hermann, Wolfgang W Huber. Enhancement of glutathione and g-glutamylcysteine synthetase, the rate limiting enzyme of glutathione synthesis, by chemoprotective plant-derived food and beverage components in the human hepatoma cell line HepG2.
Nutrition and cancer.
2003; 45(1):74-83. doi:
10.1207/s15327914nc4501_9
. [PMID: 12791507] - A G Shepherd, M M Manson, H W Ball, L I McLellan. Regulation of rat glutamate-cysteine ligase (gamma-glutamylcysteine synthetase) subunits by chemopreventive agents and in aflatoxin B(1)-induced preneoplasia.
Carcinogenesis.
2000 Oct; 21(10):1827-34. doi:
10.1093/carcin/21.10.1827
. [PMID: 11023540] - J S PHILPOT, J E STANIER. The inhibition of ribonuclease by extract of privet leaves and by alpha-angelica lactone.
The Biochemical journal.
1963 May; 87(?):373-82. doi:
10.1042/bj0870373
. [PMID: 13943175]