SFE 12:1 (BioDeep_00000630627)
natural product
代谢物信息卡片
化学式: C12H22O2 (198.1619712)
中文名称: 乙酸玫瑰酯, 10-十一烯酸甲酯, (7Z)-7-癸烯-1-醇乙酸酯
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(CC/C=C/CC(C)C)(=O)OC(C)C
InChI: InChI=1S/C12H22O2/c1-3-4-5-6-7-8-9-10-11-12(13)14-2/h3H,1,4-11H2,2H3
描述信息
同义名列表
36 个代谢物同义名
ethyl (E)-7-methyl-4-nonenoate; ethyl 7-methyl-4-non-4E-enoate; SFE 12:1; isopropyl (E)-7-methyl-4-octenoate; isopropyl 7-methyl-4-oct-4E-enoate; 7-Octen-1-ol,3,7-dimethyl-, 1-acetate; 3,7-dimethyloct-7-en-1-yl acetate; Rhodinyl acetate; methyl (9Z)-undec-9-enoate; Methyl 9-undecenoate; Methyl undec-10-enoate; Methyl 10-undecenoate; Methyl undecenate; ethyl (4E)-dec-4-enoate; Ethyl 4-decenoate; ethyl (2E)-dec-2-enoate; Ethyl 2-decenoate; (3R)-3,7-dimethyloct-6-en-1-yl acetate; Citronellyl acetate; (Z)-2-Nonenyl propionate; WE(9:1(2Z)/3:0); (E)-2-Octenyl butyrate; WE(8:1(2E)/4:0); 7Z-Decenyl acetate; dec-7-enyl acetate; 5Z-Decenyl acetate; SFE(10:1(5Z)/2:0); SFE 10:1(5Z)/2:0; 4Z-Decenyl acetate; SFE(10:1(4Z)/2:0); SFE 10:1(4Z)/2:0; 3Z-Decenyl acetate; 7E-Decenyl acetate; 5E-Decenyl acetate; 4E-Decenyl acetate; 2E-Decenyl acetate
数据库引用编号
36 个数据库交叉引用编号
- ChEBI: CHEBI:87493
- ChEBI: CHEBI:179190
- ChEBI: CHEBI:179189
- ChEBI: CHEBI:179187
- ChEBI: CHEBI:179185
- PubChem: 8833
- PubChem: 11745625
- PubChem: 8138
- PubChem: 6450502
- PubChem: 5363379
- PubChem: 5363507
- PubChem: 6533180
- ChEMBL: CHEMBL1591973
- LipidMAPS: LMFA07100003
- LipidMAPS: LMFA07100002
- LipidMAPS: LMFA07011010
- LipidMAPS: LMFA07010958
- LipidMAPS: LMFA07010937
- LipidMAPS: LMFA07010868
- LipidMAPS: LMFA07010851
- LipidMAPS: LMFA07010812
- LipidMAPS: LMFA07010630
- LipidMAPS: LMFA07010603
- LipidMAPS: LMFA07010210
- LipidMAPS: LMFA07010208
- LipidMAPS: LMFA07010207
- LipidMAPS: LMFA07010206
- LipidMAPS: LMFA07010204
- LipidMAPS: LMFA07010203
- LipidMAPS: LMFA07010202
- LipidMAPS: LMFA07010201
- CAS: 141-11-7
- CAS: 111-81-9
- CAS: 94109-98-5
- CAS: 13857-03-9
- LOTUS: LTS0045725
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)
17 个相关的物种来源信息
- 282720 - Achillea aspleniifolia: 10.1007/BF02908196
- 13329 - Achillea millefolium: 10.1007/BF02908196
- 282770 - Achillea virescens: 10.1007/BF02908196
- 2706 - Citrus: LTS0045725
- 171249 - Citrus limonia: LTS0045725
- 2711 - Citrus sinensis: 10.3390/MOLECULES13061333
- 2711 - Citrus sinensis: LTS0045725
- 2759 - Eukaryota: LTS0045725
- 106047 - Leptospermum: LTS0045725
- 295139 - Leptospermum scoparium: 10.1016/J.PHYTOCHEM.2004.03.019
- 295139 - Leptospermum scoparium: LTS0045725
- 3398 - Magnoliopsida: LTS0045725
- 3931 - Myrtaceae: LTS0045725
- 23513 - Rutaceae: LTS0045725
- 35493 - Streptophyta: LTS0045725
- 58023 - Tracheophyta: LTS0045725
- 33090 - Viridiplantae: LTS0045725
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
- Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Molecular pharmacology.
2019 11; 96(5):629-640. doi:
10.1124/mol.119.115964
. [PMID: 31515284] - Anastasiya Rybak, Michael A R Meier. Acyclic diene metathesis with a monomer from renewable resources: control of molecular weight and one-step preparation of block copolymers.
ChemSusChem.
2008; 1(6):542-7. doi:
10.1002/cssc.200800047
. [PMID: 18702153] - Gerard Lligadas, Juan C Ronda, Marina Galià, Virginia Cádiz. Novel silicon-containing polyurethanes from vegetable oils as renewable resources. Synthesis and properties.
Biomacromolecules.
2006 Aug; 7(8):2420-6. doi:
10.1021/bm060402k
. [PMID: 16903691] - J J Moore, R C Cardaman, D W Lundgren. Spermine-enhanced protein phosphorylation in human placenta.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.).
1984 Jul; 176(3):313-21. doi:
10.3181/00379727-176-41877
. [PMID: 6328534] - R Geigy, L Jenni, M Kauffmann, R J Onyango, N Weiss. Identification of T. brucei-subgroup strains isolated from game.
Acta tropica.
1975; 32(3):190-205. doi:
NULL
. [PMID: 1983]