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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

Molecular Formula C6H9NOS
Molecular Weight 143.207
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chromatographic study of photolysis of aqueous cyanocobalamin solution in presence of vitamins B and C.
2004 Jan
Recent progress in understanding thiamin biosynthesis and its genetic regulation in Saccharomyces cerevisiae.
2006 Aug
Vitamin B1 de novo synthesis in the human malaria parasite Plasmodium falciparum depends on external provision of 4-amino-5-hydroxymethyl-2-methylpyrimidine.
2006 Jan
Biosynthesis of thiamin thiazole: determination of the regiochemistry of the S/O acyl shift by using 1,4-dideoxy-D-xylulose-5-phosphate.
2006 May 19
The genes and enzymes involved in the biosynthesis of thiamin and thiamin diphosphate in yeasts.
2008
The ADP-dependent sugar kinase family: kinetic and evolutionary aspects.
2009 Jul
Combining specificity determining and conserved residues improves functional site prediction.
2009 Jun 9
The vitamin B1 metabolism of Staphylococcus aureus is controlled at enzymatic and transcriptional levels.
2009 Nov 3
New structural insights and molecular-modelling studies of 4-methyl-5-beta-hydroxyethylthiazole kinase from Pyrococcus horikoshii OT3 (PhThiK).
2009 Oct 1
Synthesis and odor evaluation of five new sulfur-containing ester flavor compounds from 4-ethyloctanoic acid.
2010 Jul 29
Domain organization in Candida glabrata THI6, a bifunctional enzyme required for thiamin biosynthesis in eukaryotes.
2010 Nov 16
Variation of some fermentative sulfur compounds in Italian "millesime" classic sparkling wines during aging and storage on lees.
2010 Sep 8
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:56:46 GMT 2023
Edited
by admin
on Fri Dec 15 18:56:46 GMT 2023
Record UNII
3XYV4I47I8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-METHYL-5-THIAZOLEETHANOL
FHFI   MI  
Systematic Name English
HEMINEURINE
Common Name English
FEMA NO. 3204
Code 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 Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
Code System Code Type Description
DRUG BANK
DB02969
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
JECFA MONOGRAPH
964
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
MERCK INDEX
m7469
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY Merck Index
CHEBI
17957
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
PUBCHEM
1136
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
FDA UNII
3XYV4I47I8
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
CAS
137-00-8
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID3044382
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
MESH
C012572
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-272-6
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
NSC
23262
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
NSC
41831
Created by admin on Fri Dec 15 18:56:46 GMT 2023 , Edited by admin on Fri Dec 15 18:56:46 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE