U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C11H12N4O2S
Molecular Weight 264.304
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFAPERIN

SMILES

CC1=CN=C(NS(=O)(=O)C2=CC=C(N)C=C2)N=C1

InChI

InChIKey=DZQVFHSCSRACSX-UHFFFAOYSA-N
InChI=1S/C11H12N4O2S/c1-8-6-13-11(14-7-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)

HIDE SMILES / InChI

Originator

Curator's Comment: reference retrieved from http://www.drugfuture.com/chemdata/Sulfaperine.html

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
SULFAPERINE

Approved Use

Unknown

Launch Date

1958
PubMed

PubMed

TitleDatePubMed
Synthesis of (+)-8-deoxyvernolepin and its 11,13-dihydroderivative. A novel reaction initiated by sulfene elimination leads to the 2-Oxa-cis-decalin skeleton.
2002 Aug 9
Preparation of alpha-sulfenyl enones by thermal fragmentation of beta-sulfenyl enol triflates.
2002 Mar 21
Amination and [2,3]-sigmatropic rearrangement of propargylic sulfides using a ketomalonate-derived oxaziridine: synthesis of N-allenylsulfenimides.
2003 Sep 21
Direct organocatalytic asymmetric alpha-sulfenylation of activated C-H bonds in lactones, lactams, and beta-dicarbonyl compounds.
2005 Sep 19
Catalytic enantio- and diastereoselective formation of beta-sultones: ring-strained precursors for enantioenriched beta-hydroxysulfonyl derivatives.
2007
Proteins protect lipid membranes from oxidation by thiyl radicals.
2007 Mar 15
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
2007 Nov 14
Comparison of benzene, nitrobenzene, and dinitrobenzene 2-arylsulfenylpyrroles.
2007 Sep 14
Regioselective hydroxysulfenylation of alpha,beta-unsaturated imines: enhanced stability of an intermediate radical.
2008
Synthesis of 4'-substituted cordycepins via benzenesulfenylation at the 4'-position as a key step.
2009
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
SULFAPERIN
INN   MART.   WHO-DD  
INN  
Official Name English
BT-325
Code English
Sulfaperin [WHO-DD]
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-(5-METHYL-2-PYRIMIDINYL)-
Systematic Name English
SULFAPERINE [MI]
Common Name English
SULFANILAMIDE, N1-(5-METHYL-2-PYRIMIDINYL)-
Systematic Name English
sulfaperin [INN]
Common Name English
4-AMINO-N-(5-METHYL-2-PYRIMIDINYL)BENZENESULFONAMIDE
Systematic Name English
SULFAPERIN [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC J01ED06
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
NCI_THESAURUS C29739
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
Code System Code Type Description
DRUG BANK
DB13320
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
PRIMARY
SMS_ID
100000083275
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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PUBCHEM
68933
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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FDA UNII
W5E840UV9P
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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ChEMBL
CHEMBL2105499
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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EVMPD
SUB10720MIG
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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DRUG CENTRAL
2522
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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INN
1399
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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EPA CompTox
DTXSID2057782
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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NCI_THESAURUS
C72854
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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ECHA (EC/EINECS)
209-976-4
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
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MERCK INDEX
m10335
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
PRIMARY Merck Index
CAS
599-88-2
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
PRIMARY
WIKIPEDIA
SULFAPERIN
Created by admin on Sat Dec 16 16:20:19 GMT 2023 , Edited by admin on Sat Dec 16 16:20:19 GMT 2023
PRIMARY