Confertin (BioDeep_00000002783)

PANOMIX_OTCML-2023 natural product

代谢物信息卡片

Anhydrocumanin

化学式: C15H20O3 (248.14123700000002)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C=C1C(=O)OC2CC(C)C3CCC(=O)C3(C)CC12
InChI: InChI=1S/C15H20O3/c1-8-6-12-10(9(2)14(17)18-12)7-15(3)11(8)4-5-13(15)16/h8,10-12H,2,4-7H2,1,3H3/t8-,10+,11-,12+,15-/m0/s1

描述信息

A natural product found in Inula hupehensis.
A pseudoguaianolide that is decahydroazuleno[6,5-b]furan-2(3H)-one substituted by an oxo group at position 5, methyl groups at positions 4a and 8 and a methylidene group at position 3. It has been isolated from the aerial parts of Inula hupehensis.

同义名列表

2 个代谢物同义名

Confertin; Anhydrocumanin

数据库引用编号

17 个数据库交叉引用编号

ChEBI: CHEBI:69342
ChEBI: CHEBI:3856
KEGG: C09378
PubChem: 167852
PubChem: 619106
Metlin: METLIN67645
ChEMBL: CHEMBL1911140
KNApSAcK: C00021138
CAS: 19908-69-1
PMhub: MS000004972
MetaboLights: MTBLC69342
MetaboLights: MTBLC3856
PubChem: 11569
KNApSAcK: C00003237
3DMET: B02912
NIKKAJI: J15.768F
LOTUS: LTS0017036

分类词条

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)

13 个相关的物种来源信息

2067512 - Ambrosia confertiflora:
1873156 - Ambrosia dumosa: 10.1055/S-0029-1240681
2364176 - Ambrosia monogyra: 10.1016/0031-9422(91)84213-C
1532261 - Ambrosia tenuifolia: 10.1055/S-0029-1240681
4210 - Asteraceae: LTS0017036
119173 - Carpesium cernuum: 10.1002/HLCA.200900275
557631 - Chiliadenus candicans: 10.1021/NP50098A011
1532790 - Dittrichia graveolens:
1805964 - Inula hupehensis: 10.1021/NP200319X
3398 - Magnoliopsida: LTS0017036
557669 - Pentanema divaricatum: 10.1002/PTR.1258
56534 - Pulicaria: LTS0017036
58023 - Tracheophyta: LTS0017036

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

Tareq Abu-Izneid, Abdur Rauf, Muhammad Saleem, Nashwa Mansour, Mohamed I S Abdelhady, Munjed M Ibrahim, Seema Patel. Urease inhibitory potential of extracts and active phytochemicals of Hypochaeris radicata (Asteraceae). Natural product research. 2020 Feb; 34(4):553-557. doi: 10.1080/14786419.2018.1489387. [PMID: 30317858]
Wilmer H Perera, Kumudini M Meepa, Frank R Fronczek, Daniel D Cook, David E Wedge, Stephen O Duke. Bioassay-Guided Isolation and Structure Elucidation of Fungicidal and Herbicidal Compounds from Ambrosia salsola (Asteraceae). Molecules (Basel, Switzerland). 2019 Feb; 24(5):. doi: 10.3390/molecules24050835. [PMID: 30813648]
Ping-an Liu, Min Liu, Wei-wei Pan, Wei-jun He, Shuai Peng, Xiao-jiang Zhou. [Study on Chemical Constituents from Carpesium abrotanoides]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2014 Dec; 37(12):2213-5. doi: . [PMID: 26080506]
M Sano. Subcellular localizations of guanylate cyclase and 3',5'-cyclic nucleotide phosphodiesterase in sea urchin sperm. Biochimica et biophysica acta. 1976 Apr; 428(2):525-31. doi: 10.1016/0304-4165(76)90061-1. [PMID: 6049]
A L Misra, J Vardy, R Bloch, S J Mulé, G A Deneau. Pharmacokinetics and metabolism of (-)-alpha-[2-3H]acetylmethadol (LAAM) in the monkey: evidence for a new metabolite. The Journal of pharmacy and pharmacology. 1976 Apr; 28(4):316-8. doi: 10.1111/j.2042-7158.1976.tb04164.x. [PMID: 6726]
R U Beĭsembaev, R Zh Dzhustupova. [Analysis of sheep blood serum haptoglobin]. Biokhimiia (Moscow, Russia). 1975 Nov; 40(6):1163-7. doi: NULL. [PMID: 2330]