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Details

Stereochemistry ACHIRAL
Molecular Formula C12H14N4O4S
Molecular Weight 310.329
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFADIMETHOXINE

SMILES

COC1=CC(NS(=O)(=O)C2=CC=C(N)C=C2)=NC(OC)=N1

InChI

InChIKey=ZZORFUFYDOWNEF-UHFFFAOYSA-N
InChI=1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)

HIDE SMILES / InChI
Molecular Formula C12H14N4O4S
Molecular Weight 310.329
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:36 UTC 2023
Edited
by admin
on Fri Dec 15 15:02:36 UTC 2023
Record UNII
30CPC5LDEX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFADIMETHOXINE
GREEN BOOK   INN   JAN   MART.   MI   USP   USP-RS   WHO-DD  
INN  
Official Name English
SULFADIMETHOXINE [MI]
Common Name English
N(SUP 1)-(2,6-DIMETHOXY-4-PYRIMIDINYL)SULFANILAMIDE
Systematic Name English
SULFADIMETHOXINE [MART.]
Common Name English
SULFADIMETHOXINE [USP-RS]
Common Name English
NSC-683544
Code English
SULFADIMETHOXINE [JAN]
Common Name English
sulfadimethoxine [INN]
Common Name English
SULPHADIMETHOXINE
Common Name English
SULFADIMETHOXINE [GREEN BOOK]
Common Name English
SULFADIMETHOXINE [USP IMPURITY]
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-(2,6-DIMETHOXY-4-PYRIMIDINYL)-
Systematic Name English
SULFADIMETHOXINE [USP MONOGRAPH]
Common Name English
Sulfadimethoxine [WHO-DD]
Common Name English
NSC-757860
Code English
Classification Tree Code System Code
CFR 21 CFR 520.2220
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
WHO-VATC QJ01EQ59
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 556.640
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220B
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
WHO-VATC QP51AG02
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
WHO-VATC QJ01EW09
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220C
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
WHO-VATC QJ01EQ09
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
WHO-ATC J01ED01
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220D
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220A
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 522.2220
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220E
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
CFR 21 CFR 520.2220F
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
Code System Code Type Description
SMS_ID
100000083246
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
CHEBI
32161
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
RXCUI
10172
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
204-523-7
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
ChEMBL
CHEMBL62193
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
NSC
757860
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
RS_ITEM_NUM
1626001
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
INN
840
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
EPA CompTox
DTXSID1023607
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
WIKIPEDIA
SULFADIMETHOXINE
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
DAILYMED
30CPC5LDEX
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
EVMPD
SUB10698MIG
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
DRUG BANK
DB06150
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
FDA UNII
30CPC5LDEX
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
NSC
683544
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
CAS
122-11-2
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
DRUG CENTRAL
2501
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
MESH
D013412
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
MERCK INDEX
m10307
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C76975
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
PUBCHEM
5323
Created by admin on Fri Dec 15 15:02:36 UTC 2023 , Edited by admin on Fri Dec 15 15:02:36 UTC 2023
PRIMARY
Related Record Type Details
Structure of SULFADIMETHOXINE SODIUM
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of SULFANILAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 2,6-DIMETHOXY-4-AMINOPYRIMIDINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of SULFANILIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of N-ACETYLSULFANILIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of SULFADIMETHOXINE N4-ACETATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 2-HYDROXYSULFAMONOMETHOXINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of SULFADIMETHOXINE
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