Taurodeoxycholate (BioCAD00000018213)

bile blood feces urine intestine

Metabolite Card

Formula: C26H45NO6S (499.2967)
SMILES: [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)NCCS(O)(=O)=O

Synonyms [en]

Taurodeoxycholate; Taurodeoxycholic Acid; Deoxytaurocholate; Taurodeoxycholic acid sodium salt; Sodium Taurodeoxycholate; Deoxycholyltaurine

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Taurodeoxycholate. 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: BioCAD00000018213). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Taurodeoxycholic acid is a bile salt formed in the liver by conjugation of deoxycholate with taurine, usually as the sodium salt. 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). Taurodeoxycholic acid can be found in Escherichia (PMID:30736766).

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 1180-95-6
  • CAS Registry Number: 207737-97-1
  • CAS Registry Number: 516-50-7
  • CAS Registry Number: ?516-50-7
  • PubChem: 10594
  • PubChem: 137701658
  • PubChem: 2733768
  • PubChem: 3724653
  • ChEBI: ChEBI:181392
  • ChEBI: ChEBI:9410
  • HMDB: HMDB0000896
  • HMDB: HMDB00896
  • LipidMaps: LMST05040004
  • LipidMaps: LMST05040013
  • KEGG: C05463
  • NCBI MeSH: Taurodeoxycholic Acid
  • Wikipedia: Taurodeoxycholic_acid
  • RefMet: RM0135855
  • MoNA: CCMSLIB00005435485
  • MoNA: CCMSLIB00005435486
  • MoNA: CCMSLIB00005435487
  • MoNA: CCMSLIB00005435567
  • MoNA: CCMSLIB00005435568
  • MoNA: CCMSLIB00005435569
  • MoNA: CCMSLIB00005435570
  • MoNA: CCMSLIB00005435571
  • MoNA: CCMSLIB00005435572
  • MoNA: CCMSLIB00005435573
  • MoNA: EMBL_MCF_2_0_HRMS_Library000116
  • MoNA: EMBL_MCF_2_0_HRMS_Library000117
  • MoNA: EMBL_MCF_2_0_HRMS_Library000335
  • MoNA: HMDB0000896_ms_ms_1265
  • MoNA: HMDB0000896_ms_ms_1266
  • MoNA: HMDB0000896_ms_ms_1267
  • MoNA: MT000071
  • MoNA: RP006001
  • MoNA: RP006002
  • MoNA: RP006003
  • Metlin: METLIN_43195
  • Metlin: METLIN_57998
  • Coconut NaturalProduct: CNP0198517.2
  • Coconut NaturalProduct: CNP0198517.4

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R04487 3.5.1.24 taurodeoxycholate amidohydrolase
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Organism Source

Taxonomy Source

  1. Homo sapiens [ncbi taxid: 9606]
  2. Streptomyces nigra 452T [ncbi taxid: ]

Pathway Synthetic

pathway id name
PathBank:SMP0120468 Congenital Bile Acid Synthesis Defect Type III
PathBank:SMP0000318 Congenital Bile Acid Synthesis Defect Type III
PathBank:SMP0120697 Familial Hypercholanemia (FHCA)
PathBank:SMP0120463 Cerebrotendinous Xanthomatosis (CTX)
PathBank:SMP0120467 Congenital Bile Acid Synthesis Defect Type II
PathBank:SMP0120495 Zellweger Syndrome
PathBank:SMP0000035 Bile Acid Biosynthesis
PathBank:SMP0000314 Congenital Bile Acid Synthesis Defect Type II
PathBank:SMP0000315 Cerebrotendinous Xanthomatosis (CTX)
PathBank:SMP0087329 Bile Acid Biosynthesis
PathBank:SMP0120652 27-Hydroxylase Deficiency
PathBank:SMP0120688 Congenital Bile Acid Synthesis Defect Type III
PathBank:SMP0120477 Familial Hypercholanemia (FHCA)
PathBank:SMP0000317 Familial Hypercholanemia (FHCA)
PathBank:SMP0087236 Bile Acid Biosynthesis
PathBank:SMP0120683 Cerebrotendinous Xanthomatosis (CTX)
PathBank:SMP0120687 Congenital Bile Acid Synthesis Defect Type II
PathBank:SMP0120715 Zellweger Syndrome
PathBank:SMP0120871 27-Hydroxylase Deficiency
PathBank:SMP0000316 Zellweger Syndrome
View All Pathways