sulfamidochrysoidine Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
anti-infectives, sulfonamides 3561 103-12-8

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • sulfamidochrysoidine
  • prontosil rubrum
  • streptozon
  • parazol
  • prontosil flavum
  • prontosil red
  • red streptocide
  • streptocide
  • sulfamidochrysoidin
  • sulfonamidochrysoidine
  • Molecular weight: 291.33
  • Formula: C12H13N5O2S
  • CLOGP: 0.67
  • LIPINSKI: 0
  • HAC: 7
  • HDO: 3
  • TPSA: 136.92
  • ALOGS: -3.53
  • ROTB: 3

Drug dosage:

None

ADMET properties:

None

Approvals:

None

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

Pharmacologic Action:

SourceCodeDescription
CHEBI has role CHEBI:33281 antibiotics
CHEBI has role CHEBI:36047 antibacterial drugs
CHEBI has role CHEBI:23018 carbonate dehydratase inhibitor
CHEBI has role CHEBI:33282 antibacterials
CHEBI has role CHEBI:88188 allergenic drug

Drug Use (View source of the data)

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 9.88 acidic
pKa2 5.44 Basic
pKa3 1.55 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
Q64Q9N6Q6O UNII
C0075515 UMLSCUI
CHEBI:8464 CHEBI
66895 PUBCHEM_CID
C003359 MESH_SUPPLEMENTAL_RECORD_UI
DB00259 DRUGBANK_ID

Pharmaceutical products:

None