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Details

Stereochemistry ACHIRAL
Molecular Formula C12H13N5O2S
Molecular Weight 291.329
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of SULFAMIDOCHRYSOIDINE

SMILES

NC1=CC(N)=C(C=C1)N=NC2=CC=C(C=C2)S(N)(=O)=O

InChI

InChIKey=ABBQGOCHXSPKHJ-WUKNDPDISA-N
InChI=1S/C12H13N5O2S/c13-8-1-6-12(11(14)7-8)17-16-9-2-4-10(5-3-9)20(15,18)19/h1-7H,13-14H2,(H2,15,18,19)/b17-16+

HIDE SMILES / InChI

Molecular Formula C12H13N5O2S
Molecular Weight 291.329
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
[Gerhard Domagk. A pathologist conquers bacterial infectious diseases].
2001 Jul
Simple and sensitive method for the determination of celecoxib in human serum by high-performance liquid chromatography with fluorescence detection.
2002 Mar 5
New generation of sterically protected C18 stationary phases containing embedded urea groups for use in high-performance liquid chromatography.
2003 Feb 14
Determination of testosterone metabolites in human hepatocytes. I. Development of an on-line sample preparation liquid chromatography technique and mass spectroscopic detection of 6beta-hydroxytestosterone.
2003 Jan 25
Emerging issues in infective endocarditis.
2004 Jun
Putting theory into practice: James Black, receptor theory and the development of the beta-blockers at ICI, 1958-1978.
2006 Jan
Determination of free ertapenem in plasma and bronchoalveolar lavage by high-performance liquid chromatography with ultraviolet detection.
2006 Jan 18
[Study on bile excretion of scutellarein].
2006 Oct
Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides.
2007 Dec 1
[Return to the future 10 years later].
2007 Jun
History revisited-Prontosil red.
2008 Aug
The determinants of the antibiotic resistance process.
2009
Phosphonocarboxylates inhibit the second geranylgeranyl addition by Rab geranylgeranyl transferase.
2009 Mar 13
Lobar pneumonia treated by Musgrave Park physicians.
2009 May
A brief history of the antibiotic era: lessons learned and challenges for the future.
2010
Ochratoxin A in roasted coffee from French supermarkets and transfer in coffee beverages: comparison of analysis methods.
2010 Aug
Redox regulation of the NPR1-TGA1 system of Arabidopsis thaliana by nitric oxide.
2010 Aug
Variation in antiherbivore defense responses in synthetic Nicotiana allopolyploids correlates with changes in uniparental patterns of gene expression.
2010 Aug
Enterorhabdus caecimuris sp. nov., a member of the family Coriobacteriaceae isolated from a mouse model of spontaneous colitis, and emended description of the genus Enterorhabdus Clavel et al. 2009.
2010 Jul
Psychological stress-induced, IDO1-dependent tryptophan catabolism: implications on immunosuppression in mice and humans.
2010 Jul 28
Rapid metabolic profiling of Nicotiana tabacum defence responses against Phytophthora nicotianae using direct infrared laser desorption ionization mass spectrometry and principal component analysis.
2010 Jun 9
Staphylococcal peptidoglycan co-localizes with Nod2 and TLR2 and activates innate immune response via both receptors in primary murine keratinocytes.
2010 Oct 7
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:14:42 GMT 2023
Edited
by admin
on Sat Dec 16 04:14:42 GMT 2023
Record UNII
Q64Q9N6Q6O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFAMIDOCHRYSOIDINE
MI   WHO-DD  
Common Name English
Sulfamidochrysoidine [WHO-DD]
Common Name English
SULFAMIDOCHRYSOIDINE [MI]
Common Name English
BENZENESULFONAMIDE, 4-(2-(2,4-DIAMINOPHENYL)DIAZENYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29739
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
Code System Code Type Description
CAS
103-12-8
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
MERCK INDEX
m10325
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Prontosil
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
EVMPD
SUB128550
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
DRUG CENTRAL
3561
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
SMS_ID
100000154362
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
CHEBI
8464
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-081-2
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
FDA UNII
Q64Q9N6Q6O
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID60145608
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
PUBCHEM
66895
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY
NCI_THESAURUS
C98270
Created by admin on Sat Dec 16 04:14:42 GMT 2023 , Edited by admin on Sat Dec 16 04:14:42 GMT 2023
PRIMARY NCIT