Asebogenin (BioDeep_00000007398)
Main id: BioDeep_00000265939
human metabolite PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C16H16O5 (288.0998)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=C(C=C2)O)O
InChI: InChI=1S/C16H16O5/c1-21-12-8-14(19)16(15(20)9-12)13(18)7-4-10-2-5-11(17)6-3-10/h2-3,5-6,8-9,17,19-20H,4,7H2,1H3
数据库引用编号
16 个数据库交叉引用编号
- ChEBI: CHEBI:2871
- KEGG: C09471
- PubChem: 442255
- HMDB: HMDB0132899
- Metlin: METLIN52347
- ChEMBL: CHEMBL253257
- CAS: 520-42-3
- PMhub: MS000020746
- PubChem: 11662
- LipidMAPS: LMPK12120545
- KNApSAcK: C00000940
- 3DMET: B02998
- NIKKAJI: J367.549A
- RefMet: Asebogenin
- KNApSAcK: 2871
- LOTUS: LTS0185548
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)
31 个相关的物种来源信息
- 4345 - Ericaceae: LTS0185548
- 188487 - Etlingera: LTS0185548
- 188496 - Etlingera littoralis: 10.3987/COM-10-12131
- 188496 - Etlingera littoralis: LTS0185548
- 2759 - Eukaryota: LTS0185548
- 85174 - Francoaceae: LTS0185548
- 23281 - Greyia: LTS0185548
- 377273 - Greyia flanaganii: 10.1016/J.PHYMED.2011.03.013
- 377273 - Greyia flanaganii: LTS0185548
- 9606 - Homo sapiens: -
- 4447 - Liliopsida: LTS0185548
- 3398 - Magnoliopsida: LTS0185548
- 352187 - Peperomia macrostachya:
- 7115 - Pieris: LTS0185548
- 317406 - Pieris japonica: 10.1021/NP049698A
- 317406 - Pieris japonica: LTS0185548
- 13215 - Piper: LTS0185548
- 130377 - Piper aduncum:
- 130377 - Piper aduncum: 10.1016/S0968-0896(03)00406-1
- 130377 - Piper aduncum: 10.1021/NP50103A003
- 130377 - Piper aduncum: 10.3136/FSTI9596T9798.3.285
- 130377 - Piper aduncum: LTS0185548
- 538297 - Piper longicaudatum: 10.1055/S-2001-11517
- 538297 - Piper longicaudatum: LTS0185548
- 16739 - Piperaceae: LTS0185548
- 164274 - Pityrogramma calomelanos: 10.1515/ZNC-1982-3-430
- 4346 - Rhododendron: 10.1016/S0031-9422(00)98660-6
- 35493 - Streptophyta: LTS0185548
- 58023 - Tracheophyta: LTS0185548
- 33090 - Viridiplantae: LTS0185548
- 4642 - Zingiberaceae: LTS0185548
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
- M Fatih Polat. Synthesis of Asebogenin and Balsacone A Precursor by a Novel Synthetic Strategy: Recent Opportunities for and Challenges of Total Synthesis of Balsacone A.
Molecules (Basel, Switzerland).
2022 May; 27(11):. doi:
10.3390/molecules27113523
. [PMID: 35684462] - Cristiano Soleo Funari, Fernanda Patrícia Gullo, Assunta Napolitano, Renato Lajarim Carneiro, Maria José Soares Mendes-Giannini, Ana Marisa Fusco-Almeida, Sonia Piacente, Cosimo Pizza, Dulce Helena Siqueira Silva. Chemical and antifungal investigations of six Lippia species (Verbenaceae) from Brazil.
Food chemistry.
2012 Dec; 135(3):2086-94. doi:
10.1016/j.foodchem.2012.06.077
. [PMID: 22953960] - Cristiano Soleo Funari, Thais Gaban Passalacqua, Daniel Rinaldo, Assunta Napolitano, Michela Festa, Anna Capasso, Sonia Piacente, Cosimo Pizza, Maria Claudia Marx Young, Giselda Durigan, Dulce Helena Siqueira Silva. Interconverting flavanone glucosides and other phenolic compounds in Lippia salviaefolia Cham. ethanol extracts.
Phytochemistry.
2011 Nov; 72(16):2052-61. doi:
10.1016/j.phytochem.2011.07.004
. [PMID: 21871644] - M B Mapunya, A A Hussein, B Rodriguez, N Lall. Tyrosinase activity of Greyia flanaganii (Bolus) constituents.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2011 Aug; 18(11):1006-12. doi:
10.1016/j.phymed.2011.03.013
. [PMID: 21680165] - A Quílez, B Berenguer, G Gilardoni, C Souccar, S de Mendonça, L F S Oliveira, M J Martín-Calero, G Vidari. Anti-secretory, anti-inflammatory and anti-Helicobacter pylori activities of several fractions isolated from Piper carpunya Ruiz & Pav.
Journal of ethnopharmacology.
2010 Apr; 128(3):583-9. doi:
10.1016/j.jep.2010.01.060
. [PMID: 20152892] - Guang-Min Yao, Yu Ding, Jian-Ping Zuo, Hong-Bing Wang, Yu-Bo Wang, Bing-Yang Ding, Pauline Chiu, Guo-Wei Qin. Dihydrochalcones from the leaves of Pieris japonica.
Journal of natural products.
2005 Mar; 68(3):392-6. doi:
10.1021/np049698a
. [PMID: 15787442] - A S Joshi, X C Li, A C Nimrod, H N elSohly, L A Walker, A M Clark. Dihydrochalcones from Piper longicaudatum.
Planta medica.
2001 Mar; 67(2):186-8. doi:
10.1055/s-2001-11517
. [PMID: 11301876] - C Lans, T Harper, K Georges, E Bridgewater. Medicinal and ethnoveterinary remedies of hunters in Trinidad.
BMC complementary and alternative medicine.
2001; 1(?):10. doi:
10.1186/1472-6882-1-10
. [PMID: 11737880] - J Orjala, A D Wright, H Behrends, G Folkers, O Sticher, H Rüegger, T Rali. Cytotoxic and antibacterial dihydrochalcones from Piper aduncum.
Journal of natural products.
1994 Jan; 57(1):18-26. doi:
10.1021/np50103a003
. [PMID: 8158163]