3alpha,7alpha,12alpha-Trihydroxy-5beta-cholestan-26-al (BioCAD00000004083)
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Metabolite Card
Formula: C27H46O4 (434.3396)
SMILES: [H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCCC(C)C=O
Synonyms [en]
3alpha,7alpha,12alpha-Trihydroxy-5beta-cholestan-26-al; 3,7,12-trihydroxycholestan-26-al; (3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxycholestan-26-al; 3-alpha-7-alpha-12-alpha-trihydroxy-5-beta-cholestan-26-al; 3a,7a,12a-Trihydroxy-5b-cholestan-26-al; 3 alpha,7-alpha,12 alpha-trihydroxy-5 beta-cholestan-26-al
Last reviewed on 2024-06-28.
Cite this Page
3alpha,7alpha,12alpha-Trihydroxy-5beta-cholestan-26-al. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000004083). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
3alpha,7alpha,12alpha-Trihydroxy-5beta-cholestan-26-al is an intermediate in bile acid biosynthesis. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues (PMID: 11316487, 16037564, 12576301, 11907135). 3a,7a,12a-trihydroxy-5b-cholestane-27-al is an enzymatically generated intermediate in the oxidation process of 5b-cholestane-3a,7a,12a,27-tetrol into 3a,7a,12a-trihydroxy-5b-cholestanoic acid in liver mitochondria. Mitochondrial sterol 27-hydroxylase (EC 1.14.13.60) appears to perform multiple monooxygenations in this conversion. (PMID: 8496170).
DBLinks
- CAS Registry Number: 3836-01-9
- PubChem CID: 439479
- ChEBI: 16466
- HMDB: HMDB0003533
- LipidMaps: LMST04030164
- KEGG: C01301
- BioCyc: 3-ALPHA7-ALPHA12-ALPHA-TRIHYDROX
- NCBI MeSH: 3,7,12-trihydroxycholestan-26-al
- Wikipedia:
Other DBLinks
- CAS Registry Number: 114883-29-3
- CAS Registry Number: 128241-03-2
- CAS Registry Number: 129464-60-4
- CAS Registry Number: 3836-01-9
- PubChem: 439479
- ChEBI: ChEBI:16466
- HMDB: HMDB0003533
- LipidMaps: LMST04030164
- KEGG: C01301
- BioCyc: 3-ALPHA7-ALPHA12-ALPHA-TRIHYDROX
- NCBI MeSH: 3,7,12-trihydroxycholestan-26-al
- RefMet: RM0033575
- Metlin: METLIN_57926
- Coconut NaturalProduct: CNP0082935.1
- Coconut NaturalProduct: CNP0325880.1
- Coconut NaturalProduct: CNP0339006.1
Class / Ontology
- WishartLab ClassyFire: [Bile acids, alcohols and derivatives] Bile acids, alcohols and derivatives
- RefMet: [Cholesterols] Cholesterols
- LipidMaps: [C27 bile acids, alcohols, and derivatives [ST0403]] C27 bile acids, alcohols, and derivatives [ST0403]
- ChEBI: [CHEBI:16466] 3alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-al
- Coconut NaturalProduct: [Cholestane steroids] Cholestane steroids
- Coconut NaturalProduct: [Monacolins and Monacolin derivatives] Monacolins and Monacolin derivatives
| ID | EC Number | Name |
|---|---|---|
| KEGG:R03506 | 3alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-al:NAD+ 26-oxidoreductase | |
| KEGG:R03507 | 1.14.15.15 | C05446 + C00007 + 2 C00080 + 2 C00662<=>C01301 + 2 C00001 + 2 C00667 |
| KEGG:R08759 | 1.14.15.15 | C05446<=>C01301 |
| KEGG:R08761 | 1.14.15.15 | C01301 + C00007 + 2 C00080 + 2 C00662<=>C04722 + C00001 + 2 C00667 |
| BioCyc:CHOLESTANETETRAOL-26-DEHYDROGENASE-RXN | 5-BETA-CHOLESTANE-3-ALPHA7-TETRAOL + OXYGEN-MOLECULE + 2 Reduced-adrenal-ferredoxins + 2 PROTON --> 3-ALPHA7-ALPHA12-ALPHA-TRIHYDROX + 2 WATER + 2 Oxidized-adrenal-ferredoxins | |
| BioCyc:1.2.1.40-RXN | 3α,7α,12α-trihydroxycholestan-26-al 26-hydroxylase |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-556833 | Metabolism of lipids |
| Reactome:R-BTA-194068 | Bile acid and bile salt metabolism |
| Reactome:R-CFA-1430728 | Metabolism |
| Reactome:R-CFA-556833 | Metabolism of lipids |
| Reactome:R-CFA-194068 | Bile acid and bile salt metabolism |
| Reactome:R-DRE-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-HSA-194068 | Bile acid and bile salt metabolism |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-8957322 | Metabolism of steroids |
| Reactome:R-RNO-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-SSC-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-BTA-8957322 | Metabolism of steroids |
| Reactome:R-CFA-8957322 | Metabolism of steroids |
| Reactome:R-DRE-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-MMU-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-RNO-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-SSC-1430728 | Metabolism |