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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2O2
Molecular Weight 126.1133
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THYMINE

SMILES

CC1=CNC(=O)NC1=O

InChI

InChIKey=RWQNBRDOKXIBIV-UHFFFAOYSA-N
InChI=1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9)

HIDE SMILES / InChI
Molecular Formula C5H6N2O2
Molecular Weight 126.1133
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2010
465
PubMed

PubMed

TitleDatePubMed
Protection by ultraviolet A and B sunscreens against in situ dipyrimidine photolesions in human epidermis is comparable to protection against sunburn.
2000 Jul
Mechanisms and implications of the age-associated decrease in DNA repair capacity.
2000 Jul
Adenine-induced selective apoptosis toward HIV chronically infected cells in vitro.
2000 Jul 14
Ionization mechanism of oligonucleotides in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2001
Phylogeny, function, and evolution of the cupins, a structurally conserved, functionally diverse superfamily of proteins.
2001 Apr
Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder.
2001 Apr 15
15-mer DNA duplexes containing an abasic site are thermodynamically more stable with adjacent purines than with pyrimidines.
2001 Apr 3
Metastable decay of negatively charged oligodeoxynucleotides analyzed with ultraviolet matrix-assisted laser desorption/ionization post-source decay and deuterium exchange.
2001 Feb
5-Formyluracil and its nucleoside derivatives confer toxicity and mutagenicity to mammalian cells by interfering with normal RNA and DNA metabolism.
2001 Feb 3
Mutagenic effects of 5-formyluracil on a plasmid vector during replication in Escherichia coli.
2001 Jan
The transport of a reversible proton pump antagonist, 5, 6-dimethyl-2-(4-Fluorophenylamino)-4-(1-methyl-1,2,3, 4-tetrahydroisoquinoline-2-yl) pyrimidine hydrochloride (YH1885), across caco-2 cell monolayers.
2001 Jan
Interferon gamma-dependent induction of thymidine phosphorylase/platelet-derived endothelial growth factor through gamma-activated sequence-like element in human macrophages.
2001 Jan 15
Conformation and dynamics of abasic sites in DNA investigated by time-resolved fluorescence of 2-aminopurine.
2001 Jan 30
Synthesis of 1-(2-deoxy-beta-D-ribofuranosyl)-2,4-difluoro-5-substituted-benzenes: "thymine replacement" analogs of thymidine for evaluation as anticancer and antiviral agents.
2001 Jan-Feb
Solution structure of an A-tract DNA bend.
2001 Mar 9
Fragmentation mechanisms of oligodeoxynucleotides: effects of replacing phosphates with methylphosphonates and thymines with other bases in T-rich sequences.
2001 May
Recognition and kinetics for excision of a base lesion within clustered DNA damage by the Escherichia coli proteins Fpg and Nth.
2001 May 15
Insight into the catalytic mechanism of DNA polymerase beta: structures of intermediate complexes.
2001 May 8
Patents

Patents

05955610
1
06084082
1
06156894
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:00:18 GMT 2023
Edited
by admin
on Fri Dec 15 15:00:18 GMT 2023
Record UNII
QR26YLT7LT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THYMINE
INCI   MI   WHO-DD  
INCI  
Official Name English
5-METHYL URACIL
Systematic Name English
ZIDOVUDINE RELATED COMPOUND C
USP-RS  
Common Name English
THYMINE [USP IMPURITY]
Common Name English
Thymine [WHO-DD]
Common Name English
STAVUINE IMPURITY A [WHO-IP]
Common Name English
THYMINE [INCI]
Common Name English
ZIDOVUDINE RELATED COMPOUND C [USP-RS]
Common Name English
THYMIN
Systematic Name English
ZIDOVUDINE IMPURITY C [WHO-IP]
Common Name English
ZIDOVUDINE IMPURITY C [EP IMPURITY]
Common Name English
ZIDOVUDINE RELATED COMPOUND C [USP IMPURITY]
Common Name English
NSC-168663
Code English
5-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE (THYMINE)
Common Name English
NSC-14705
Code English
THYMINE [MI]
Common Name English
5-METHYL-1,2,3,4-TETRAHYDROPYRIMIDINE-2,4-DIONE
Systematic Name English
Classification Tree Code System Code
LOINC 48157-2
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
LOINC 75153-7
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
LOINC 75121-4
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
NCI_THESAURUS C789
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
Code System Code Type Description
FDA UNII
QR26YLT7LT
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
MERCK INDEX
m10823
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY Merck Index
PUBCHEM
1135
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
CAS
65-71-4
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
NSC
168663
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
MESH
D013941
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-616-1
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
SMS_ID
100000091723
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
DRUG BANK
DB03462
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
NCI_THESAURUS
C881
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
RS_ITEM_NUM
1724532
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
DAILYMED
QR26YLT7LT
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
CHEBI
17821
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID4052342
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
WIKIPEDIA
THYMINE
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
RXCUI
1368871
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY RxNorm
NSC
14705
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
EVMPD
SUB27112
Created by admin on Fri Dec 15 15:00:18 GMT 2023 , Edited by admin on Fri Dec 15 15:00:18 GMT 2023
PRIMARY
Related Record Type Details
Structure of STAVUDINE
PARENT -> METABOLITE
Structure of BAIBA, (R)-
METABOLITE -> PARENT
BAIBA induces energy expenditure in adipocytes and distal fat tissues, and β-oxidation of hepatic fatty acids in part via activation of peroxisome proliferators-activated receptor α (PPARα) [33]. Notably, in humans, plasma BAIBA concentrations increase with exercise and are inversely associated with metabolic risk factors.
Related Record Type Details
Structure of STAVUDINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of STAVUDINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of ZIDOVUDINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of STAVUDINE
PARENT -> IMPURITY
Amount Not Specified
INTERNATIONAL PHARMACOPEIA
Structure of STAVUDINE
PARENT -> IMPURITY
Calculation of percentage contents: – correction factor: multiply the peak area of impurity A by 0.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of THYMINE
ACTIVE MOIETY
NIH
NCATS
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ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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