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Details

Stereochemistry ACHIRAL
Molecular Formula C6H9NOS
Molecular Weight 143.207
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-METHYL-5-THIAZOLEETHANOL

SMILES

CC1=C(CCO)SC=N1

InChI

InChIKey=BKAWJIRCKVUVED-UHFFFAOYSA-N
InChI=1S/C6H9NOS/c1-5-6(2-3-8)9-4-7-5/h4,8H,2-3H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Domain organization in Candida glabrata THI6, a bifunctional enzyme required for thiamin biosynthesis in eukaryotes.
2010-11-16
Variation of some fermentative sulfur compounds in Italian "millesime" classic sparkling wines during aging and storage on lees.
2010-09-08
Synthesis and odor evaluation of five new sulfur-containing ester flavor compounds from 4-ethyloctanoic acid.
2010-07-29
The vitamin B1 metabolism of Staphylococcus aureus is controlled at enzymatic and transcriptional levels.
2009-11-03
New structural insights and molecular-modelling studies of 4-methyl-5-beta-hydroxyethylthiazole kinase from Pyrococcus horikoshii OT3 (PhThiK).
2009-10-01
The ADP-dependent sugar kinase family: kinetic and evolutionary aspects.
2009-07
Combining specificity determining and conserved residues improves functional site prediction.
2009-06-09
The genes and enzymes involved in the biosynthesis of thiamin and thiamin diphosphate in yeasts.
2008
Non-empirical study of the phosphorylation reaction catalyzed by 4-methyl-5-beta-hydroxyethylthiazole kinase: relevance of the theory of intermolecular interactions.
2007-07
Thiazole synthase from Escherichia coli: an investigation of the substrates and purified proteins required for activity in vitro.
2007-06-15
Effect of pH on the Maillard reaction of [13C5]xylose, cysteine, and thiamin.
2007-02-21
Structure of the thiazole biosynthetic enzyme THI1 from Arabidopsis thaliana.
2006-10-13
Recent progress in understanding thiamin biosynthesis and its genetic regulation in Saccharomyces cerevisiae.
2006-08
Biosynthesis of thiamin thiazole: determination of the regiochemistry of the S/O acyl shift by using 1,4-dideoxy-D-xylulose-5-phosphate.
2006-05-19
Vitamin B1 de novo synthesis in the human malaria parasite Plasmodium falciparum depends on external provision of 4-amino-5-hydroxymethyl-2-methylpyrimidine.
2006-01
Chromatographic study of photolysis of aqueous cyanocobalamin solution in presence of vitamins B and C.
2004-01
Patents

Patents

Name Type Language
4-METHYL-5-THIAZOLEETHANOL
FHFI   MI  
Systematic Name English
FEMA NO. 3204
Preferred Name English
HEMINEURINE
Common Name English
NSC-41831
Code English
THIAMINE THIOZOLE
Common Name English
4-METHYL-5-THIAZOLYLETHANOL
Systematic Name English
NSC-23262
Code English
4-METHYL-5-(2-HYDROXYETHYL)THIAZOLE
Systematic Name English
2-(4-METHYL-1,3-THIAZOL-5-YL)ETHANOL
Systematic Name English
2-(4-METHYLTHIAZOLE-5-YL)ETHANOL
Systematic Name English
4-METHYL-5-THIAZOLE ETHANOL [FCC]
Common Name English
5-THIAZOLEETHANOL, 4-METHYL-
Systematic Name English
4-METHYL-5-(.BETA.-HYDROXYETHYL)THIAZOLE
Systematic Name English
5-(2-HYDROXYETHYL)-4-METHYLTHIAZOLE
Systematic Name English
5-(HYDROXYETHYL)-4-METHYLTHIAZOLE
Systematic Name English
4-METHYL-5-THIAZOLEETHANOL [FHFI]
Common Name English
5-(.BETA.-HYDROXYETHYL)-4-METHYLTHIAZOLE
Systematic Name English
4-METHYL-5-THIAZOLEETHANOL [MI]
Common Name English
2-(4-METHYL-5-THIAZOLYL)ETHANOL
Systematic Name English
4-METHYL-5-THIAZOLE ETHANOL
FCC  
Common Name English
SULFUROL
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 4-METHYL-5-THIAZOLEETHANOL
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
Code System Code Type Description
DRUG BANK
DB02969
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
JECFA MONOGRAPH
964
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
MERCK INDEX
m7469
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY Merck Index
CHEBI
17957
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
PUBCHEM
1136
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
FDA UNII
3XYV4I47I8
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
CAS
137-00-8
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID3044382
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
MESH
C012572
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-272-6
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
NSC
23262
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY
NSC
41831
Created by admin on Mon Mar 31 19:27:15 GMT 2025 , Edited by admin on Mon Mar 31 19:27:15 GMT 2025
PRIMARY