thalianol (BioDeep_00000013088)
Secondary id: BioDeep_00001871086
代谢物信息卡片
化学式: C30H50O (426.386145)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(lipidomics) 11.76%
分子结构信息
SMILES: C1[C@@]2(C)[C@@]([H])(CCC3[C@@](C)([C@H](C)CC/C=C(\C)/CC/C=C(\C)/C)CCC2=3)C(C)(C)[C@@H](O)C1
InChI: InChI=1S/C30H50O/c1-21(2)11-9-12-22(3)13-10-14-23(4)29(7)19-17-25-24(29)15-16-26-28(5,6)27(31)18-20-30(25,26)8/h11,13,23,26-27,31H,9-10,12,14-20H2,1-8H3/b22-13+/t23-,26+,27+,29-,30-/m1/s1
数据库引用编号
11 个数据库交叉引用编号
- ChEBI: CHEBI:52317
- ChEBI: CHEBI:181945
- KEGG: C19832
- PubChem: 25229600
- PubChem: 56928123
- PubChem: 74409384
- Metlin: METLIN53808
- LipidMAPS: LMPR0106240002
- MetaCyc: CPD-10263
- PMhub: MS000027473
- PubChem: 135626299
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
17 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
NAD(P)H + O2 + thalianol ⟶ H2O + NAD(P)+ + a thalian-diol
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(15)
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
- thalianol and derivatives biosynthesis:
(3S)-2,3-epoxy-2,3-dihydrosqualene ⟶ thalianol
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。
文献列表
- Hainan Zhao, Mingyu Yang, Jade Bishop, Yuhan Teng, Yingxue Cao, Brandon D Beall, Shuanglin Li, Tongxin Liu, Qingxi Fang, Chao Fang, Haoyang Xin, Hans-Wilhelm Nützmann, Anne Osbourn, Fanli Meng, Jiming Jiang. Identification and functional validation of super-enhancers in Arabidopsis thaliana.
Proceedings of the National Academy of Sciences of the United States of America.
2022 11; 119(48):e2215328119. doi:
10.1073/pnas.2215328119
. [PMID: 36409894] - Dandan Li, Xiaoyang Bi, Jingjing Ma, Xiaohong Zhang, Keni Jiang, Xuezhen Zhu, Jiguang Huang, Lijuan Zhou. Natural herbicidal alkaloid berberine regulates the expression of thalianol and marneral gene clusters in Arabidopsis thaliana.
Pest management science.
2022 Jul; 78(7):2896-2908. doi:
10.1002/ps.6914
. [PMID: 35415871] - Zhenhua Liu, Jitender Cheema, Marielle Vigouroux, Lionel Hill, James Reed, Pirita Paajanen, Levi Yant, Anne Osbourn. Formation and diversification of a paradigm biosynthetic gene cluster in plants.
Nature communications.
2020 10; 11(1):5354. doi:
10.1038/s41467-020-19153-6
. [PMID: 33097700] - Nan Yu, Hans-Wilhelm Nützmann, James T MacDonald, Ben Moore, Ben Field, Souha Berriri, Martin Trick, Susan J Rosser, S Vinod Kumar, Paul S Freemont, Anne Osbourn. Delineation of metabolic gene clusters in plant genomes by chromatin signatures.
Nucleic acids research.
2016 Mar; 44(5):2255-65. doi:
10.1093/nar/gkw100
. [PMID: 26895889] - Ben Field, Anna-Sophie Fiston-Lavier, Ariane Kemen, Katrin Geisler, Hadi Quesneville, Anne E Osbourn. Formation of plant metabolic gene clusters within dynamic chromosomal regions.
Proceedings of the National Academy of Sciences of the United States of America.
2011 Sep; 108(38):16116-21. doi:
10.1073/pnas.1109273108
. [PMID: 21876149] - Ben Field, Anne E Osbourn. Metabolic diversification--independent assembly of operon-like gene clusters in different plants.
Science (New York, N.Y.).
2008 Apr; 320(5875):543-7. doi:
10.1126/science.1154990
. [PMID: 18356490] - . .
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. doi:
. [PMID: 15125655]