General
Preferred name
vinblastine
Synonyms
VINBLASTINE SULFATE ()
NSC49842 ()
Vinblastine (sulfate) ()
Vincaleukoblastine sulfate salt ()
NSC-47842 ()
Velban ()
[3H]-Vinblastine ()
Vinblastine sulphate ()
Velbe ()
29060LE ()
VLB monosulfate ()
Vincaleukoblastine sulfate ()
29060-LE ()
Alkaban-aq ()
Vinblast,lederle ()
NSC-49842 ()
Vinblastini sulfas ()
P&D ID
PD013748
CAS
865-21-4
18556-44-0
132142-72-4
143-67-9
Tags
natural product
drug
available
Approved by
FDA
First approval
1965
Drug Status
approved
Drug indication
Antineoplastic
Solid tumour/cancer
Max Phase
Phase 4
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION A pan tubulin inhibitor that is a chemical analogue of (from Catharanthus roseus, also known as Vinca rosea). There is some ambiguity surrounding the exact stereochemistry of vinblastine. The chirality shown here corresponds to the PubChem CID provided on the Summary tab. However, bioactivity data for the compound is also listed against CID 241903, and some of the external resource links refer to this chiral specification or others. Marketed formulations contain vinblastine sulfate (PubChem CID 5388983). (GtoPdb)
Cell lines
610
Organisms
4
Compound Sets
25
Cayman Chemical Bioactives
CeMM library of unique drugs (CLOUD)
ChEMBL Approved Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Reference compounds for characterizing cellular injury in high-content cellular morphology assays
ReFrame library
External IDs
57
Properties
(calculated by RDKit )
Molecular Weight
810.42
Hydrogen Bond Acceptors
12
Hydrogen Bond Donors
3
Rotatable Bonds
7
Ring Count
9
Aromatic Ring Count
3
cLogP
3.99
TPSA
154.1
Fraction CSP3
0.59
Chiral centers
10.0
Largest ring
9.0
QED
0.18
Structural alerts
1
Tubulin modulation
Nuisance compounds in cellular assays
Custom attributes
(extracted from source data)
MOA
tubulin polymerization inhibitor
AChR inhibitor
Tubulin modulator
Microtubule assembly inhibitor
microtubule inhibitor, tubulin polymerization inhibitor
Target
Tubulin
nAChR
JUN, TUBA1A, TUBB, TUBD1, TUBE1, TUBG1
Microtubule/Tubulin
Pathway
Neuroscience
Autophagy
Cell Cycle/DNA Damage
cytoskeleton
Member status
virtual
Disease Area
hematologic malignancy, infectious disease, oncology
Indication
Hodgkin's lymphoma, true histiocytic lymphoma (THL), mycosis, small lymphocytic lymphoma (SLL), testicular carcinoma, Kaposi sarcoma
Cellular injury category
Cytoskeletal
Therapeutic Class
Anticancer Agents
Source data