(3S,6aR,6bS,8aR,9R,14bR)-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-eicosahydro-picene-3,9-diol (BioDeep_00000897704)
Main id: BioDeep_00000013033
代谢物信息卡片
化学式: C30H50O2 (442.3811)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)C)O)C)C
InChI: InChI=1S/C30H50O2/c1-25(2)17-20-19-9-10-22-28(6)13-12-23(31)26(3,4)21(28)11-14-30(22,8)29(19,7)16-15-27(20,5)24(32)18-25/h9,20-24,31-32H,10-18H2,1-8H3/t20?,21?,22?,23-,24+,27+,28-,29+,30+/m0/s1
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
12 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- soybean saponin I biosynthesis:
β-amyrin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + an oxidized [NADPH-hemoprotein reductase] + sophoradiol
- soybean saponin I biosynthesis:
β-amyrin + H+ + NADPH + O2 ⟶ H2O + NADP+ + sophoradiol
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(10)
- soybean saponin I biosynthesis:
24-hydroxy-β-amyrin + H+ + NADPH + O2 ⟶ H2O + NADP+ + soyasapogenol B
- soybean saponin I biosynthesis:
24-hydroxy-β-amyrin + H+ + NADPH + O2 ⟶ H2O + NADP+ + soyasapogenol B
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
- soybean saponin I biosynthesis:
24-hydroxy-β-amyrin + H+ + NADPH + O2 ⟶ H2O + NADP+ + soyasapogenol B
- soybean saponin I biosynthesis:
24-hydroxy-β-amyrin + H+ + NADPH + O2 ⟶ H2O + NADP+ + soyasapogenol B
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
- soybean saponin I biosynthesis:
UDP-α-D-glucuronate + soyasapogenol B ⟶ H+ + UDP + soyasapogenol B-3-O-β-glucuronide
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 个相关的物种来源信息
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
- Nihong Lu, Yongrui Yang, Jun Liu, Jie Li, Bing Ouyang, Jiawei Xia, Yingrong Du. Sophoradiol inhibits the growth of drug resistant Mycobacterium tuberculosis in vitro and murine models of tuberculosis.
Microbial pathogenesis.
2020 Apr; 141(?):103971. doi:
10.1016/j.micpath.2020.103971
. [PMID: 31923558] - Jing Lu, Jia-Hong Sun, Yao Tan, Yoshihiro Kano, Dan Yuan. New triterpenoid saponins from the flowers of Pueraria thomsonii.
Journal of Asian natural products research.
2013; 15(10):1065-72. doi:
10.1080/10286020.2013.802690
. [PMID: 24168266] - Muhammad R Habib, Muhammad R Karim. Effect of anhydrosophoradiol-3-acetate of Calotropis gigantea (Linn.) flower as antitumoric agent against Ehrlich's ascites carcinoma in mice.
Pharmacological reports : PR.
2013; 65(3):761-7. doi:
10.1016/s1734-1140(13)71057-0
. [PMID: 23950602] - Yukio Fujiwara, Naoko Kiyota, Keita Motomura, Katsumi Mera, Motohiro Takeya, Tsuyoshi Ikeda, Ryoji Nagai. Some natural compounds enhance N epsilon-(carboxymethyl)lysine formation.
Annals of the New York Academy of Sciences.
2008 Apr; 1126(?):152-4. doi:
10.1196/annals.1433.015
. [PMID: 18079486] - Masaaki Shibuya, Masaki Hoshino, Yuji Katsube, Hiroaki Hayashi, Tetsuo Kushiro, Yutaka Ebizuka. Identification of beta-amyrin and sophoradiol 24-hydroxylase by expressed sequence tag mining and functional expression assay.
The FEBS journal.
2006 Mar; 273(5):948-59. doi:
10.1111/j.1742-4658.2006.05120.x
. [PMID: 16478469] - Norio Nakamura. [Inhibitory effects of some traditional medicines on proliferation of HIV-1 and its protease].
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
2004 Aug; 124(8):519-29. doi:
10.1248/yakushi.124.519
. [PMID: 15297721] - Nam-Cheol Kim, Darrick S H L Kim, A Douglas Kinghorn. New triterpenoids from the leaves of Abrus precatorius.
Natural product letters.
2002 Aug; 16(4):261-6. doi:
10.1080/10575630290020596
. [PMID: 12168762]