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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H16N2O4
Molecular Weight 252.2664
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of (NORTH)-METHANOCARBATHYMIDINE

SMILES

CC1=CN([C@H]2C[C@H](O)[C@]3(CO)C[C@H]23)C(=O)NC1=O

InChI

InChIKey=NOWRLNPOENZFHP-ARHDFHRDSA-N
InChI=1S/C12H16N2O4/c1-6-4-14(11(18)13-10(6)17)8-2-9(16)12(5-15)3-7(8)12/h4,7-9,15-16H,2-3,5H2,1H3,(H,13,17,18)/t7-,8+,9+,12+/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H16N2O4
Molecular Weight 252.2664
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:17:05 GMT 2023
Edited
by admin
on Sat Dec 16 10:17:05 GMT 2023
Record UNII
LTM5S02010
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(NORTH)-METHANOCARBATHYMIDINE
Common Name English
NORTH-METHANOCARBATHYMIDINE
Common Name English
2,4(1H,3H)-PYRIMIDINEDIONE, 1-((1S,2S,4S,5R)-4-HYDROXY-5-(HYDROXYMETHYL)BICYCLO(3.1.0)HEX-2-YL)-5-METHYL-
Systematic Name English
2,4(1H,3H)-PYRIMIDINEDIONE, 1-(4-HYDROXY-5-(HYDROXYMETHYL)BICYCLO(3.1.0)HEX-2-YL)-5-METHYL-, (1S-(1.ALPHA.,2.ALPHA.,4.BETA.,5.ALPHA.))-
Systematic Name English
1-((1S,2S,4S,5R)-4-HYDROXY-5-(HYDROXYMETHYL)BICYCLO(3.1.0)HEX-2-YL)-5-METHYL-2,4(1H,3H)-PYRIMIDINEDIONE
Systematic Name English
N-MCT
Common Name English
N-METHANOCARBATHYMIDINE
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 426014
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
Code System Code Type Description
PUBCHEM
445212
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
CAS
156126-12-4
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
WIKIPEDIA
North-methanocarbathymidine
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
CHEBI
46026
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
FDA UNII
LTM5S02010
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID301028076
Created by admin on Sat Dec 16 10:17:05 GMT 2023 , Edited by admin on Sat Dec 16 10:17:05 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY