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

Stem definitionDrug idCAS RN
uridine derivatives used as antiviral agents and as antineoplastics 3042 59-14-3

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • broxuridine
  • bromodeoxyuridine
  • 5-Bromodeoxyuridine
A nucleoside that substitutes for thymidine in DNA and thus acts as an antimetabolite. It causes breaks in chromosomes and has been proposed as an antiviral and antineoplastic agent. It has been given orphan drug status for use in the treatment of primary brain tumors.
  • Molecular weight: 307.10
  • Formula: C9H11BrN2O5
  • CLOGP: -0.68
  • LIPINSKI: 0
  • HAC: 7
  • HDO: 3
  • TPSA: 99.10
  • ALOGS: -1.18
  • ROTB: 2

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
MeSH PA D000890 Anti-Infective Agents
MeSH PA D000963 Antimetabolites
MeSH PA D000964 Antimetabolites, Antineoplastic
MeSH PA D000970 Antineoplastic Agents
MeSH PA D000998 Antiviral Agents
MeSH PA D009676 Noxae
MeSH PA D011838 Radiation-Sensitizing Agents
CHEBI has role CHEBI:35221 antimetabolite
CHEBI has role CHEBI:35610 antineoplastic agents

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 7.88 acidic
pKa2 13.02 acidic
pKa3 13.7 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Thymidine kinase, cytosolic Kinase Ki 5.30 CHEMBL
Thymidylate kinase Kinase Ki 5.30 CHEMBL

External reference:

IDSource
D01763 KEGG_DRUG
C0006233 UMLSCUI
CHEBI:472552 CHEBI
CHEMBL222280 ChEMBL_ID
DB12028 DRUGBANK_ID
6035 PUBCHEM_CID
3462 INN_ID
G34N38R2N1 UNII
D001973 MESH_DESCRIPTOR_UI
U33 PDB_CHEM_ID

Pharmaceutical products:

None