Dihydrocarvone (BioDeep_00000267359)

Secondary id: BioDeep_00000008636, BioDeep_00000014732, BioDeep_00000267345

代谢物信息卡片

2-Methyl-5-(1-methylethenyl)cyclohexanone, 9ci

化学式: C10H16O (152.12010859999998)
中文名称: (E)-2-甲基-5-(1-甲基乙烯基)环己酮, (+)-二氢香芹酮, 2-甲基-5-(1-甲基乙烯基)环己酮
谱图信息: 最多检出来源 Macaca mulatta(otcml) 6.22%

分子结构信息

SMILES: C1(=O)[C@@H](CC[C@H](C1)C(=C)C)C
InChI: InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h8-9H,1,4-6H2,2-3H3

描述信息

A dihydrocarvone in (R,R) configuration.
A dihydrocarvone resulting from reduction of the endocyclic cyclohexene double bond.

同义名列表

16 个代谢物同义名

(1R,4R)-Dihydrocarvone; (E)-Dihydrocarvone; (+)-dihydrocarvone; Dihydrocarvone; 2-Methyl-5-(1-methylethenyl)cyclohexanone, 9ci; 2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one; 2-Methyl-5-(1-methylethenyl)-cyclohexanone; 2-Methyl-5-(1-methylvinyl)cyclohexan-1-one; 2-Methyl-5-(1-methylethenyl)cyclohexanone; 2-Methyl-5-(prop-1-en-2-yl)cyclohexanone; 2-Methyl-5-isopropenylcyclohexanone; 5-Isopropenyl-2-methylcyclohexanone; p-Menth-8(9)-en-2-one; 1,6-Dihydrocarvone; 8-p-Menthen-2-one; FEMA 3565

数据库引用编号

23 个数据库交叉引用编号

ChEBI: CHEBI:154
ChEBI: CHEBI:23733
KEGG: C11398
KEGG: C18018
PubChem: 22227
PubChem: 24473
Metlin: METLIN91250
ChEMBL: CHEMBL2268553
LipidMAPS: LMPR0102090033
KNApSAcK: C00037051
KNApSAcK: C00033439
CAS: 5524-05-0
CAS: 5948-04-9
CAS: 7764-50-3
PMhub: MS000022292
MetaboLights: MTBLC154
MetaboLights: MTBLC23733
PubChem: 13572
3DMET: B04244
NIKKAJI: J995.644A
PubChem: 96024238
NIKKAJI: J150.037F
NIKKAJI: J87.284I

分类词条

Menthane monoterpenoids [PR010209]

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)

32 个相关的物种来源信息

3483 Cannabis sativa: 10.1021/NP50008A001
354530 Zanthoxylum schinifolium: 10.1021/JF0728101
555479 Nigella sativa: 10.1515/ZNC-2003-9-1004
1268187 Origanum cordifolium: 10.1016/0378-8741(91)90063-J
87257 Evernia prunastri: 10.1021/JF60201A022
87674 Eucalyptus nitens: 10.1016/S0031-9422(00)94539-4
1082757 Origanum syriacum: 10.1080/10412905.1991.9697923
40922 Anethum graveolens:
751869 Thymus broussonetii: 10.1080/10412905.1993.9698169
751874 Thymus saturejoides: 10.1080/10412905.1993.9698169
29719 Mentha spicata: 10.1016/0031-9422(90)85103-M
501610 Agathosma betulina: 10.1021/JF60201A021
169607 Tagetes minuta: 10.1007/BF02536610
1205795 Trachyspermum anethifolium: 10.1080/0972060X.2014.989187
79837 Cymbopogon martinii: 10.1016/0305-1978(88)90091-9
1192317 Poiretia latifolia: 10.1590/S0103-50532010000500003
3483 Cannabis sativa: 10.1021/NP50008A001
354530 Zanthoxylum schinifolium: 10.1021/JF0728101
555479 Nigella sativa: 10.1515/ZNC-2003-9-1004
1268187 Origanum cordifolium: 10.1016/0378-8741(91)90063-J
87257 Evernia prunastri: 10.1021/JF60201A022
87674 Eucalyptus nitens: 10.1016/S0031-9422(00)94539-4
1082757 Origanum syriacum: 10.1080/10412905.1991.9697923
40922 Anethum graveolens:
751869 Thymus broussonetii: 10.1080/10412905.1993.9698169
751874 Thymus saturejoides: 10.1080/10412905.1993.9698169
29719 Mentha spicata: 10.1016/0031-9422(90)85103-M
501610 Agathosma betulina: 10.1021/JF60201A021
169607 Tagetes minuta: 10.1007/BF02536610
1205795 Trachyspermum anethifolium: 10.1080/0972060X.2014.989187
79837 Cymbopogon martinii: 10.1016/0305-1978(88)90091-9
1192317 Poiretia latifolia: 10.1590/S0103-50532010000500003

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

Erika Yoshida, Motoki Kojima, Munenori Suzuki, Fumio Matsuda, Kazutaka Shimbo, Akiko Onuki, Yousuke Nishio, Yoshihiro Usuda, Akihiko Kondo, Jun Ishii. Increased carvone production in Escherichia coli by balancing limonene conversion enzyme expression via targeted quantification concatamer proteome analysis. Scientific reports. 2021 11; 11(1):22126. doi: 10.1038/s41598-021-01469-y. [PMID: 34764337]
Facundo Marconi, María Laura Umpiérrez, David Gonzalez, Sonia Rodríguez Giordano, Paula Rodriguez. Endophytic biocatalysts with enoate reductase activity isolated from Mentha pulegium. World journal of microbiology & biotechnology. 2018 Mar; 34(4):50. doi: 10.1007/s11274-018-2434-7. [PMID: 29550961]
Hwa-Jeong Yeom, Jae Soon Kang, Gil-Hah Kim, Il-Kwon Park. Insecticidal and acetylcholine esterase inhibition activity of Apiaceae plant essential oils and their constituents against adults of German cockroach (Blattella germanica). Journal of agricultural and food chemistry. 2012 Jul; 60(29):7194-203. doi: 10.1021/jf302009w. [PMID: 22746406]
Ghalbane Ichrak, Belaqziz Rim, Ait Said Loubna, Oufdou Khalid, Romane Abderrahmane, El Messoussi Said. Chemical composition, antibacterial and antioxidant activities of the essential oils from Thymus satureioides and Thymus pallidus. Natural product communications. 2011 Oct; 6(10):1507-10. doi: ". [PMID: 22164795]
Bharti Sapra, Subheet Jain, A K Tiwary. Percutaneous permeation enhancement by terpenes: mechanistic view. The AAPS journal. 2008; 10(1):120-32. doi: 10.1208/s12248-008-9012-0. [PMID: 18446512]
Recep Kotan, Saban Kordali, Ahmet Cakir. Screening of antibacterial activities of twenty-one oxygenated monoterpenes. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2007 Jul; 62(7-8):507-13. doi: 10.1515/znc-2007-7-808. [PMID: 17913064]
H Isaacs, J J Heffron, M Badenhorst. 'Picture frame' fibres in a carrier of the trait for malignant hyperpyrexia. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde. 1975 Nov; 49(46):1923-6. doi: NULL. [PMID: 795]