lividomycin 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
antibiotics, produced by Streptomyces strains 1589 36441-41-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • mannosyldeoxyparomomycin
  • lividomycin
  • Lividomycin A
  • Quintomycin B
  • Molecular weight: 761.78
  • Formula: C29H55N5O18
  • CLOGP: -8.26
  • LIPINSKI: 3
  • HAC: 23
  • HDO: 15
  • TPSA: 406.24
  • ALOGS: -1.06
  • ROTB: 12

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:33231 antitubercular agents
CHEBI has role CHEBI:33282 bactericides
CHEBI has role CHEBI:25212 metabolites

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 12.52 acidic
pKa2 13.34 acidic
pKa3 13.74 acidic
pKa4 13.95 acidic
pKa5 8.21 Basic
pKa6 7.75 Basic
pKa7 7.14 Basic
pKa8 6.54 Basic
pKa9 5.88 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
C0994406 UMLSCUI
CHEBI:71960 CHEBI
LIV PDB_CHEM_ID
CHEMBL389029 ChEMBL_ID
C100306 MESH_SUPPLEMENTAL_RECORD_UI
3575 INN_ID
A606AJ494W UNII
72394 PUBCHEM_CID
DB04728 DRUGBANK_ID

Pharmaceutical products:

None