sulfamidochrysoidine 🐶 Veterinary Use | 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

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
CHEBI has role CHEBI:33281 antibiotics
CHEBI has role CHEBI:36047 antibacterial drugs
CHEBI has role CHEBI:23018 EC 4.2.1.1 inhibitor
CHEBI has role CHEBI:33282 bactericides
CHEBI has role CHEBI:88188 allergenic drug

Drug Use | Suggest Off label Use Form| |View source of the data|

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

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