Cholestane (BioDeep_00000407592)

   

natural product Bile acids


代谢物信息卡片


(1S,2S,7R,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane

化学式: C27H48 (372.3756)
中文名称: 5α-胆甾烷
谱图信息: 最多检出来源 Homo sapiens(bile_acids) 97.14%

Reviewed

Last reviewed on 2024-07-19.

Cite this Page

Cholestane. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/cholestane (retrieved 2024-12-23) (BioDeep RN: BioDeep_00000407592). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4C3(CCCC4)C)C
InChI: InChI=1S/C27H48/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h19-25H,6-18H2,1-5H3

描述信息

同义名列表

8 个代谢物同义名

Cholestane; (1S,2S,7R,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane; 28,29,30-Trinorlanostane; 5alpha-Cholestane (8ci); (5alpha)-Cholestane; 5alpha-Cholestane; alpha-Cholestane; (5a)-Cholestane



数据库引用编号

26 个数据库交叉引用编号

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)

24 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
Cytoplasm 12 ANXA5, BCL2, CASP3, CLMN, CYP3A4, MTOR, NT5C2, PIK3CA, PTGS2, PTK2B, PTPN1, SGCB
Peripheral membrane protein 6 ANXA5, AP1S2, CYP1B1, MTOR, PTGS2, PTPN1
Endosome membrane 1 LDLR
Endoplasmic reticulum membrane 8 BCL2, CYP1B1, CYP3A4, CYP7A1, HMGCR, MTOR, PTGS2, PTPN1
Nucleus 4 BCL2, CASP3, MTOR, PTK2B
cytosol 10 ANXA5, AP1S2, BCL2, CASP3, MTOR, NT5C2, PIK3CA, PTK2B, PTPN1, RICTOR
dendrite 2 MTOR, PTK2B
phagocytic vesicle 1 MTOR
nucleoplasm 2 CASP3, MTOR
Cell membrane 1 LDLR
Cytoplasmic side 3 AP1S2, MTOR, PTPN1
lamellipodium 2 PIK3CA, PTK2B
Multi-pass membrane protein 1 HMGCR
Golgi apparatus membrane 1 MTOR
cell cortex 1 PTK2B
cell surface 1 LDLR
glutamatergic synapse 3 CASP3, PTK2B, PTPN1
Golgi apparatus 3 AP1S2, LDLR, RICTOR
Golgi membrane 3 AP1S2, INS, MTOR
growth cone 1 PTK2B
lysosomal membrane 2 AP1S2, MTOR
neuronal cell body 2 CASP3, PTK2B
postsynapse 1 PTPN1
sarcolemma 2 ANXA5, SGCB
Cytoplasm, cytosol 1 NT5C2
Lysosome 2 LDLR, MTOR
Presynapse 1 PTK2B
plasma membrane 5 LDLR, PIK3CA, PTK2B, SGCB, SLC10A2
Membrane 9 ANXA5, BCL2, CLMN, CYP1B1, CYP3A4, HMGCR, LDLR, MTOR, PTPN1
apical plasma membrane 1 SLC10A2
basolateral plasma membrane 1 LDLR
caveola 1 PTGS2
extracellular exosome 1 ANXA5
Lysosome membrane 1 MTOR
endoplasmic reticulum 4 BCL2, HMGCR, PTGS2, PTPN1
extracellular space 1 INS
perinuclear region of cytoplasm 2 PIK3CA, PTK2B
Schaffer collateral - CA1 synapse 1 PTK2B
intercalated disc 1 PIK3CA
mitochondrion 2 BCL2, CYP1B1
protein-containing complex 3 BCL2, PTGS2, PTPN1
intracellular membrane-bounded organelle 4 AP1S2, CYP1B1, CYP3A4, CYP7A1
Microsome membrane 5 CYP1B1, CYP3A4, CYP7A1, MTOR, PTGS2
postsynaptic density 2 CASP3, PTK2B
TORC1 complex 1 MTOR
TORC2 complex 2 MTOR, RICTOR
Single-pass type I membrane protein 1 LDLR
Secreted 1 INS
extracellular region 2 ANXA5, INS
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 3 BCL2, CYP7A1, LDLR
mitochondrial outer membrane 2 BCL2, MTOR
mitochondrial matrix 1 PTPN1
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 2 ANXA5, LDLR
low-density lipoprotein particle 1 LDLR
dendritic spine 1 PTK2B
Early endosome 3 AP1S2, LDLR, PTPN1
Membrane, clathrin-coated pit 2 AP1S2, LDLR
apical part of cell 1 LDLR
clathrin-coated pit 2 AP1S2, LDLR
Single-pass type II membrane protein 1 SGCB
Cell membrane, sarcolemma 1 SGCB
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 SGCB
focal adhesion 2 ANXA5, PTK2B
peroxisomal membrane 1 HMGCR
Nucleus, PML body 1 MTOR
PML body 1 MTOR
collagen-containing extracellular matrix 1 ANXA5
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 2 CLMN, PTGS2
Late endosome 1 LDLR
receptor complex 1 LDLR
Zymogen granule membrane 1 ANXA5
neuron projection 1 PTGS2
cytoskeleton 2 PTK2B, SGCB
mitochondrial crista 1 PTPN1
postsynaptic density, intracellular component 1 PTK2B
nuclear envelope 1 MTOR
Endomembrane system 4 AP1S2, LDLR, MTOR, PTPN1
endosome lumen 2 INS, PTPN1
sorting endosome 2 LDLR, PTPN1
microvillus 1 SLC10A2
Cytoplasmic vesicle membrane 1 AP1S2
cell body 1 PTK2B
myelin sheath 1 BCL2
Peroxisome membrane 1 HMGCR
trans-Golgi network membrane 1 AP1S2
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 INS, PTGS2
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
Single-pass type IV membrane protein 1 CLMN
vesicle membrane 1 ANXA5
clathrin-coated endocytic vesicle membrane 1 LDLR
NMDA selective glutamate receptor complex 1 PTK2B
endolysosome membrane 1 LDLR
apical dendrite 1 PTK2B
death-inducing signaling complex 1 CASP3
AP-type membrane coat adaptor complex 1 AP1S2
membrane coat 1 AP1S2
dystrophin-associated glycoprotein complex 1 SGCB
sarcoglycan complex 1 SGCB
AP-1 adaptor complex 1 AP1S2
somatodendritic compartment 1 LDLR
Cytoplasmic vesicle, phagosome 1 MTOR
meiotic nuclear membrane microtubule tethering complex 1 CLMN
PCSK9-LDLR complex 1 LDLR
endothelial microparticle 1 ANXA5
BAD-BCL-2 complex 1 BCL2
cytoplasmic side of endoplasmic reticulum membrane 1 PTPN1
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


文献列表

  • Debora Esposito, Slavko Komarnytsky, Sue Shapses, Ilya Raskin. Anabolic effect of plant brassinosteroid. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2011 Oct; 25(10):3708-19. doi: 10.1096/fj.11-181271. [PMID: 21746867]
  • Rodrigo T Iborra, Adriana Machado-Lima, Gabriela Castilho, Valeria S Nunes, Dulcinéia S P Abdalla, Edna R Nakandakare, Marisa Passarelli. Advanced glycation in macrophages induces intracellular accumulation of 7-ketocholesterol and total sterols by decreasing the expression of ABCA-1 and ABCG-1. Lipids in health and disease. 2011 Sep; 10(?):172. doi: 10.1186/1476-511x-10-172. [PMID: 21957962]
  • Debora Esposito, Thirumurugan Rathinasabapathy, Alexander Poulev, Slavko Komarnytsky, Ilya Raskin. Akt-dependent anabolic activity of natural and synthetic brassinosteroids in rat skeletal muscle cells. Journal of medicinal chemistry. 2011 Jun; 54(12):4057-66. doi: 10.1021/jm200028h. [PMID: 21491949]
  • L J Chen, Y F Lu, J T Chien, B H Chen. Formation and inhibition of cholesterol oxidation products in tea-leaf eggs during marinating. Journal of agricultural and food chemistry. 2010 Oct; 58(19):10467-74. doi: 10.1021/jf102487j. [PMID: 20828157]
  • Hongmei Liu, Tiebing Wang, Kaixun Huang. Cholestane-3beta,5alpha,6beta-triol-induced reactive oxygen species production promotes mitochondrial dysfunction in isolated mice liver mitochondria. Chemico-biological interactions. 2009 May; 179(2-3):81-7. doi: 10.1016/j.cbi.2008.12.003. [PMID: 19121293]
  • Ying Zhang, Herbert J Tobias, J Thomas Brenna. Steroid isotopic standards for gas chromatography-combustion isotope ratio mass spectrometry (GCC-IRMS). Steroids. 2009 Mar; 74(3):369-78. doi: 10.1016/j.steroids.2008.10.001. [PMID: 18992268]
  • Sandy Mosig, Knut Rennert, Petra Büttner, Siegfried Krause, Dieter Lütjohann, Muhidien Soufi, Regine Heller, Harald Funke. Monocytes of patients with familial hypercholesterolemia show alterations in cholesterol metabolism. BMC medical genomics. 2008 Nov; 1(?):60. doi: 10.1186/1755-8794-1-60. [PMID: 19040724]
  • Giorgio Gilli, Renato Rovere, Deborah Traversi, Tiziana Schilirò, Cristina Pignata. Faecal sterols determination in wastewater and surface water. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2006 Oct; 843(1):120-4. doi: 10.1016/j.jchromb.2006.05.022. [PMID: 16787764]
  • Vikas Kumar G Shah, Hugh Dunstan, Warren Taylor. An efficient diethyl ether-based soxhlet protocol to quantify faecal sterols from catchment waters. Journal of chromatography. A. 2006 Mar; 1108(1):111-5. doi: 10.1016/j.chroma.2005.12.084. [PMID: 16430911]
  • Thy T Truong, Philip J Marriott, Nichola A Porter, Rhys Leeming. Application of comprehensive two-dimensional gas chromatography to the quantification of overlapping faecal sterols. Journal of chromatography. A. 2003 Nov; 1019(1-2):197-210. doi: 10.1016/s0021-9673(03)00766-0. [PMID: 14650615]