Urocortisol (BioDeep_00000637531)

Main id: BioDeep_00000002839

 

PANOMIX_OTCML-2023


代谢物信息卡片


3alpha,11beta,17,21-tetrahydroxy-5beta-pregnan-20-one

化学式: C21H34O5 (366.2406)
中文名称: 四氢皮质醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC12CCC(CC1CCC3C2C(CC4(C3CCC4(C(=O)CO)O)C)O)O
InChI: InChI=1S/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18-,19+,20+,21+/m1/s1

描述信息

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Tetrahydrocortisol is cortisol metabolite. The urinary Tetrahydrocortisol/Tetrahydrocortisone ratio decreases with increasing 11β-hydroxysteroid dehydrogenase (11β-HSD) activity[1][2].

同义名列表

7 个代谢物同义名

3alpha,11beta,17,21-tetrahydroxy-5beta-pregnan-20-one; Pregnan-20-one,3,11,17,21-tetrahydroxy-, (3a,5b,11b)-; 5b-Tetrahydrocortisol; Tetrahydrocortisol; Urocortisol; ST 21:1;O5; Urocortisol



数据库引用编号

12 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)

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
Cytoplasm 5 ANG, ERC1, NR3C1, NR3C2, POMC
Peripheral membrane protein 3 CYP21A2, ERC1, GBA1
Endoplasmic reticulum membrane 6 CYP21A2, GUCY2D, HSD11B1, HSD11B2, NR3C2, SRD5A2
Nucleus 3 ANG, NR3C1, NR3C2
cytosol 5 ANG, APOA1, LEP, NR3C1, NR3C2
trans-Golgi network 1 GBA1
centrosome 2 ERC1, NR3C1
nucleoplasm 2 NR3C1, NR3C2
Multi-pass membrane protein 1 SRD5A2
Golgi apparatus membrane 1 ERC1
Synapse 3 CRH, ERC1, NR3C1
cell surface 1 PLG
glutamatergic synapse 1 PLG
Golgi apparatus 1 GBA1
Golgi membrane 2 ERC1, INS
growth cone 1 ANG
lysosomal membrane 1 GBA1
neuronal cell body 2 ANG, SRD5A2
presynaptic membrane 1 ERC1
Lysosome 1 GBA1
Presynapse 1 ERC1
plasma membrane 4 APOA1, GUCY2D, PLG, REN
Membrane 6 CYP21A2, ERC1, HSD11B1, HSD11B2, NR3C1, REN
extracellular exosome 3 APOA1, GBA1, PLG
Lysosome membrane 1 GBA1
Lumenal side 1 GBA1
endoplasmic reticulum 2 GBA1, HSD11B2
extracellular space 11 ANG, APOA1, CRH, CRP, IGF1, IL6, INS, LEP, PLG, POMC, REN
lysosomal lumen 1 GBA1
Schaffer collateral - CA1 synapse 1 PLG
mitochondrion 1 NR3C1
protein-containing complex 1 NR3C1
intracellular membrane-bounded organelle 2 HSD11B1, HSD11B2
Microsome membrane 1 CYP21A2
Single-pass type I membrane protein 1 GUCY2D
Secreted 11 ANG, APOA1, CRH, CRP, IGF1, IL6, INS, LEP, PLG, POMC, REN
extracellular region 11 ANG, APOA1, CRH, CRP, IGF1, IL6, INS, LEP, PLG, POMC, REN
Single-pass membrane protein 1 CYP21A2
mitochondrial matrix 1 NR3C1
anchoring junction 1 ERC1
photoreceptor outer segment 1 GUCY2D
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 2 ERC1, NR3C1
external side of plasma membrane 1 PLG
varicosity 1 CRH
Extracellular vesicle 1 APOA1
chylomicron 1 APOA1
high-density lipoprotein particle 1 APOA1
low-density lipoprotein particle 1 APOA1
very-low-density lipoprotein particle 1 APOA1
actin cytoskeleton 1 ANG
neuronal dense core vesicle lumen 1 CRH
perikaryon 1 CRH
cytoplasmic vesicle 1 APOA1
nucleolus 1 ANG
Early endosome 1 APOA1
apical part of cell 1 REN
Single-pass type II membrane protein 1 HSD11B1
Cytoplasm, cytoskeleton 1 ERC1
Cytoplasm, cytoskeleton, spindle 1 NR3C1
spindle 1 NR3C1
basement membrane 1 ANG
collagen-containing extracellular matrix 2 APOA1, PLG
secretory granule 1 POMC
nuclear speck 1 NR3C1
nuclear outer membrane 1 GUCY2D
receptor complex 1 NR3C2
ciliary basal body 1 ERC1
chromatin 2 NR3C1, NR3C2
Chromosome 2 ANG, NR3C1
cytoskeleton 1 ERC1
Cell projection, podosome 1 ERC1
podosome 1 ERC1
Nucleus, nucleolus 1 ANG
blood microparticle 2 APOA1, PLG
Endomembrane system 1 ERC1
endosome lumen 1 INS
cell body fiber 1 SRD5A2
Nucleus, nucleoplasm 1 NR3C1
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
Presynaptic cell membrane 1 ERC1
exocytic vesicle 1 IGF1
Microsome 1 HSD11B2
secretory granule lumen 3 APOA1, INS, POMC
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 APOA1, IL6, INS
platelet alpha granule lumen 2 IGF1, PLG
endocytic vesicle 2 ANG, APOA1
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
IkappaB kinase complex 1 ERC1
cytoskeleton of presynaptic active zone 1 ERC1
photoreceptor outer segment membrane 1 GUCY2D
[Isoform Alpha]: Cytoplasm 1 NR3C1
spherical high-density lipoprotein particle 1 APOA1
photoreceptor disc membrane 1 GUCY2D
endocytic vesicle lumen 1 APOA1
angiogenin-PRI complex 1 ANG
[Isoform Beta]: Nucleus 1 NR3C1
[Isoform Alpha-B]: Nucleus 1 NR3C1
alphav-beta3 integrin-IGF-1-IGF1R complex 1 IGF1
insulin-like growth factor binding protein complex 1 IGF1
insulin-like growth factor ternary complex 1 IGF1
interleukin-6 receptor complex 1 IL6


文献列表

  • Susanna Bianzano, Matias Nordaby, Leona Plum-Mörschel, Barbara Peil, Tim Heise. Safety, tolerability, pharmacodynamics and pharmacokinetics following once-daily doses of BI 187004, an inhibitor of 11 beta-hydroxysteroid dehydrogenase-1, over 28 days in patients with type 2 diabetes mellitus and overweight or obesity. Diabetes, obesity & metabolism. 2023 Mar; 25(3):832-843. doi: 10.1111/dom.14932. [PMID: 36478142]
  • Thi Chi Mai Tran, Thi Ngoc Anh Tran, Hoang Bich Nga Le, Viet Hoa Nguyen, Minh Dien Tran, Chi Dung Vu, Ronda F Greaves. Validation of steroid ratios for random urine by mass spectrometry to detect 5α-reductase deficiency in Vietnamese children. Clinical chemistry and laboratory medicine. 2022 07; 60(8):1225-1233. doi: 10.1515/cclm-2022-0272. [PMID: 35607271]
  • Chaelin Lee, Seung Mi Lee, Dong Jun Byun, So Yeon Kim, Hugh I Kim, Do Yup Lee, Young Mi Jung, Chan-Wook Park, Joong Shin Park, Man Ho Choi. Maternal Signatures of Cortisol in First Trimester Small-for-Gestational Age. Reproductive sciences (Thousand Oaks, Calif.). 2022 05; 29(5):1498-1505. doi: 10.1007/s43032-021-00822-w. [PMID: 35001327]
  • Stéphanie Espiard, Johanna McQueen, Mark Sherlock, Oskar Ragnarsson, Ragnhildur Bergthorsdottir, Pia Burman, Per Dahlqvist, Bertil Ekman, Britt Edén Engström, Stanko Skrtic, Jeanette Wahlberg, Paul M Stewart, Gudmundur Johannsson. Improved Urinary Cortisol Metabolome in Addison Disease: A Prospective Trial of Dual-Release Hydrocortisone. The Journal of clinical endocrinology and metabolism. 2021 03; 106(3):814-825. doi: 10.1210/clinem/dgaa862. [PMID: 33236103]
  • Katarzyna Kosicka, Anna Siemiątkowska, Dąbrówka Pałka, Agata Szpera-Goździewicz, Grzegorz H Bręborowicz, Franciszek K Główka. Detailed analysis of cortisol, cortisone and their tetrahydro- and allo-tetrahydrometabolites in human urine by LC-MS/MS. Journal of pharmaceutical and biomedical analysis. 2017 Jun; 140(?):174-181. doi: 10.1016/j.jpba.2017.03.039. [PMID: 28359965]
  • Scott P Webster, Andrew McBride, Margaret Binnie, Karen Sooy, Jonathan R Seckl, Ruth Andrew, T David Pallin, Hazel J Hunt, Trevor R Perrior, Vincent S Ruffles, J William Ketelbey, Alan Boyd, Brian R Walker. Selection and early clinical evaluation of the brain-penetrant 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor UE2343 (Xanamem™). British journal of pharmacology. 2017 03; 174(5):396-408. doi: 10.1111/bph.13699. [PMID: 28012176]
  • Luca Chiesa, Sara Panseri, Radmila Pavlovic, Francesca Tiziana Cannizzo, Bartolomeo Biolatti, Sara Divari, Roberto Villa, Francesco Arioli. HPLC-ESI-MS/MS assessment of the tetrahydro-metabolites of cortisol and cortisone in bovine urine: promising markers of dexamethasone and prednisolone treatment. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2016 Jul; 33(7):1175-89. doi: 10.1080/19440049.2016.1202453. [PMID: 27310211]
  • Laura C Torchen, Jan Idkowiak, Naomi R Fogel, Donna M O'Neil, Cedric H L Shackleton, Wiebke Arlt, Andrea Dunaif. Evidence for Increased 5α-Reductase Activity During Early Childhood in Daughters of Women With Polycystic Ovary Syndrome. The Journal of clinical endocrinology and metabolism. 2016 05; 101(5):2069-75. doi: 10.1210/jc.2015-3926. [PMID: 26990942]
  • Judith Buehlmeier, Thomas Remer, Petra Frings-Meuthen, Christiane Maser-Gluth, Martina Heer. Glucocorticoid activity and metabolism with NaCl-induced low-grade metabolic acidosis and oral alkalization: results of two randomized controlled trials. Endocrine. 2016 Apr; 52(1):139-47. doi: 10.1007/s12020-015-0730-7. [PMID: 26349936]
  • Laura I Stirrat, James R O'Reilly, Sarah M Barr, Ruth Andrew, Simon C Riley, Alexander F Howie, Maria Bowman, Roger Smith, John G Lewis, Fiona C Denison, Shareen Forbes, Jonathan R Seckl, Brian R Walker, Jane E Norman, Rebecca M Reynolds. Decreased maternal hypothalamic-pituitary-adrenal axis activity in very severely obese pregnancy: Associations with birthweight and gestation at delivery. Psychoneuroendocrinology. 2016 Jan; 63(?):135-43. doi: 10.1016/j.psyneuen.2015.09.019. [PMID: 26444587]
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  • Luigi Di Luigi, Francesco Botrè, Stefania Sabatini, Massimiliano Sansone, Monica Mazzarino, Laura Guidetti, Carlo Baldari, Andrea Lenzi, Daniela Caporossi, Francesco Romanelli, Paolo Sgrò. Acute effects of physical exercise and phosphodiesterase's type 5 inhibition on serum 11β-hydroxysteroid dehydrogenases related glucocorticoids metabolites: a pilot study. Endocrine. 2014 Dec; 47(3):952-8. doi: 10.1007/s12020-014-0185-2. [PMID: 24532078]
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