beta-Amyrin palmitate (BioDeep_00000176617)
human metabolite blood metabolite natural product
代谢物信息卡片
化学式: C46H80O2 (664.6158)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C
InChI: InChI=1S/C46H80O2/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(47)48-39-27-28-44(7)37(42(39,4)5)26-29-46(9)38(44)25-24-35-36-34-41(2,3)30-31-43(36,6)32-33-45(35,46)8/h24,36-39H,10-23,25-34H2,1-9H3
描述信息
Beta-amyrin palmitate, also known as B-amyrin palmitic acid, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amyrin palmitate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Beta-amyrin palmitate can be found in black elderberry, which makes beta-amyrin palmitate a potential biomarker for the consumption of this food product.
同义名列表
9 个代谢物同义名
4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl hexadecanoate; (4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate; 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl hexadecanoate; beta-Amyrin palmitic acid; Β-amyrin palmitic acid; b-Amyrin palmitic acid; beta-amyrin palmitate; β-Amyrin palmitate; b-Amyrin palmitate
数据库引用编号
6 个数据库交叉引用编号
- PubChem: 13915598
- HMDB: HMDB0249100
- KNApSAcK: C00045240
- foodb: FDB007028
- chemspider: 26503597
- LOTUS: LTS0232124
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)
39 个相关的物种来源信息
- 3563 - Amaranthaceae: LTS0232124
- 4037 - Apiaceae: LTS0232124
- 4044 - Apium: LTS0232124
- 4045 - Apium graveolens: LTS0232124
- 4056 - Apocynaceae: LTS0232124
- 4210 - Asteraceae: LTS0232124
- 25674 - Balanophora: LTS0232124
- 29813 - Balanophora fungosa: 10.1248/CPB.57.1352
- 29813 - Balanophora fungosa: LTS0232124
- 25673 - Balanophoraceae: LTS0232124
- 130238 - Brachylaena: LTS0232124
- 1542379 - Brachylaena ramiflora: 10.1021/NP0201220
- 1542379 - Brachylaena ramiflora: LTS0232124
- 4381 - Campanulaceae: LTS0232124
- 4305 - Celastraceae: LTS0232124
- 85180 - Celastrus: LTS0232124
- 489980 - Celastrus hypoleucus: 10.1002/HLCA.200590094
- 489980 - Celastrus hypoleucus: LTS0232124
- 1804623 - Chenopodiaceae: LTS0232124
- 212298 - Elateriospermum: LTS0232124
- 212299 - Elateriospermum tapos: 10.1016/S0031-9422(00)85245-0
- 212299 - Elateriospermum tapos: LTS0232124
- 2759 - Eukaryota: LTS0232124
- 3977 - Euphorbiaceae: LTS0232124
- 151229 - Haloxylon: LTS0232124
- 454511 - Haloxylon salicornicum: 10.1016/J.BMCL.2010.05.061
- 454511 - Haloxylon salicornicum: LTS0232124
- 9606 - Homo sapiens: -
- 41589 - Inula: LTS0232124
- 4382 - Lobelia: LTS0232124
- 308559 - Lobelia inflata: 10.1002/JPS.2600810705
- 308559 - Lobelia inflata: LTS0232124
- 3398 - Magnoliopsida: LTS0232124
- 35493 - Streptophyta: LTS0232124
- 52860 - Tabernaemontana: LTS0232124
- 52861 - Tabernaemontana divaricata: 10.1016/S0031-9422(00)94818-0
- 52861 - Tabernaemontana divaricata: LTS0232124
- 58023 - Tracheophyta: LTS0232124
- 33090 - Viridiplantae: LTS0232124
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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- S Ajikumaran Nair, B Sabulal, J Radhika, R Arunkumar, A Subramoniam. Promising anti-diabetes mellitus activity in rats of β-amyrin palmitate isolated from Hemidesmus indicus roots.
European journal of pharmacology.
2014 Jul; 734(?):77-82. doi:
10.1016/j.ejphar.2014.03.050
. [PMID: 24726843] - Ranjani Maurya, Anuj Srivastava, Priyanka Shah, Mohammad Imran Siddiqi, S M Rajendran, Anju Puri, Prem P Yadav. β-Amyrin acetate and β-amyrin palmitate as antidyslipidemic agents from Wrightia tomentosa leaves.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2012 Jun; 19(8-9):682-5. doi:
10.1016/j.phymed.2012.03.013
. [PMID: 22541636] - V S Prakash Chaturvedula, Jennifer K Schilling, James S Miller, Rabodo Andriantsiferana, Vincent E Rasamison, David G I Kingston. Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest.
Journal of natural products.
2002 Aug; 65(8):1222-4. doi:
10.1021/np0201220
. [PMID: 12193040] - Q Y Zhang, X Y Wang, H P Ying, T M Cheng, Y Y Zhao. [Studies on the chemical constituents of Carduus crispus L].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2001 Dec; 26(12):837-9. doi:
. [PMID: 12776331]
- G Kweifio-Okai, D Bird, B Field, R Ambrose, A R Carroll, P Smith, R Valdes. Antiinflammatory activity of a Ghanaian antiarthritic herbal preparation: III.
Journal of ethnopharmacology.
1995 Apr; 46(1):7-15. doi:
10.1016/0378-8741(95)01222-y
. [PMID: 7475126] - G Kweifio-Okai, D Bird, P Eu, A R Carroll, R Ambrose, B Field. Effect of alpha-amyrin palmitate on adjuvant arthritis.
Drugs under experimental and clinical research.
1994; 20(1):1-5. doi:
NULL
. [PMID: 7924889] - A Subarnas, T Tadano, Y Oshima, K Kisara, Y Ohizumi. Pharmacological properties of beta-amyrin palmitate, a novel centrally acting compound, isolated from Lobelia inflata leaves.
The Journal of pharmacy and pharmacology.
1993 Jun; 45(6):545-50. doi:
10.1111/j.2042-7158.1993.tb05596.x
. [PMID: 8103103] - A Subarnas, T Tadano, N Nakahata, Y Arai, H Kinemuchi, Y Oshima, K Kisara, Y Ohizumi. A possible mechanism of antidepressant activity of beta-amyrin palmitate isolated from Lobelia inflata leaves in the forced swimming test.
Life sciences.
1993; 52(3):289-96. doi:
10.1016/0024-3205(93)90220-w
. [PMID: 8423710]