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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14N2O4S
Molecular Weight 306.337
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEDIASULFONE

SMILES

NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(NCC(O)=O)C=C2

InChI

InChIKey=FKKUMFTYSTZUJG-UHFFFAOYSA-N
InChI=1S/C14H14N2O4S/c15-10-1-5-12(6-2-10)21(19,20)13-7-3-11(4-8-13)16-9-14(17)18/h1-8,16H,9,15H2,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C14H14N2O4S
Molecular Weight 306.337
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

PubMed

PubMed

TitleDatePubMed
Evaluation of the sulfones and streptomycin in experimental tuberculosis.
1949 Dec 14
Folate-synthesizing enzyme system as target for development of inhibitors and inhibitor combinations against Candida albicans-synthesis and biological activity of new 2,4-diaminopyrimidines and 4'-substituted 4-aminodiphenyl sulfones.
2004 Jan 1
Column and thin-layer chromatographic methods for the simultaneous determination of acediasulfone in the presence of cinchocaine, and cefuroxime in the presence of its hydrolytic degradation products.
2007 Mar-Apr
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:15:27 UTC 2023
Edited
by admin
on Fri Dec 15 16:15:27 UTC 2023
Record UNII
30YP2YHH8W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACEDIASULFONE
MI   WHO-DD  
Common Name English
N-P-SULFANILYLPHENYLGLYCINE
Common Name English
ACEDIASULFONE [MI]
Common Name English
ACEDIASULPHONE
Common Name English
Acediasulfone [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C849
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
Code System Code Type Description
WIKIPEDIA
ACEDIASULFONE
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
DRUG BANK
DB08926
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
NCI_THESAURUS
C77129
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
EVMPD
SUB00242MIG
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
FDA UNII
30YP2YHH8W
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
MERCK INDEX
m1294
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY Merck Index
CAS
80-03-5
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
SMS_ID
100000078805
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
PUBCHEM
66451
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-243-7
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
DRUG CENTRAL
44
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
MESH
C521214
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
EPA CompTox
DTXSID00229991
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY