General
Preferred name
ETOPOSIDE
Synonyms
VP-16 ()
VP-16-213 ()
Etoposide (VP-16) ()
VP-16213,Vepesid,VP-16 ()
Etoposide?(VP-16) ()
Toposar ()
Sintopozid ()
Etoposide resolution mixture ()
Etoposido ()
NSC-141540 ()
VePesid ()
Etoposidum ()
Etoposide-d3 ()
P&D ID
PD003202
CAS
33419-42-0
121471-01-0
Tags
available
drug
nuisance
Approved by
PMDA
FDA
First approval
1983
Drug indication
acute lymphoblastic leukemia
Solid tumour/cancer
Drug Status
approved
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
A DNA topoisomerase II inhibitor which is a synthetic derivative of podophyllotoxin, found in the American Mayapple (Podophyllum peltatum).
(GtoPdb)
DESCRIPTION
Etoposide (VP-16; VP-16-213) is an anti-cancer chemotherapy agent. Etoposide inhibits topoisomerase II, thus stopping DNA replication. Etoposide induces cell cycle arrest, apoptosis and autophagy[1].
PRICE
29
DESCRIPTION
Etoposide (VP-16-213) is a topoisomerase II inhibitor that inhibits DNA synthesis by forming a complex with topoisomerase II and DNA (IC50=60.3 ??M). Etoposide has antitumor activity and induces apoptosis and autophagy.
DESCRIPTION
inhibitor of topoisomerase II
(Informer Set)
DESCRIPTION
Protein kinase inhibitor
(Tocris Bioactive Compound Library)
DESCRIPTION
Topoisomerase II inhibitor
(Tocriscreen Plus)
DESCRIPTION
Etoposide is a podophyllotoxin derivative used to treat testicular and small cell lung tumors.
(Enamine Bioactive Compounds)
DESCRIPTION
Etoposide (VP-16-213) is a topoisomerase II inhibitor that inhibits DNA synthesis by forming a complex with topoisomerase II and DNA (IC50=60.3 μM). Etoposide has antitumor activity and induces apoptosis and autophagy.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
691
Organisms
3
Compound Sets
35
A Collection of Useful Nuisance Compounds (CONS) for Interrogation of Bioassay Integrity
AdooQ Bioactive Compound Library
ChEMBL Approved Drugs
ChEMBL Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
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Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine Bioactive Compounds
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
Informer Set
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Nuisance compounds in cellular assays
Prestwick Chemical Library
Reference compounds for characterizing cellular injury in high-content cellular morphology assays
ReFrame library
Selleckchem Bioactive Compound Library
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Tocris Bioactive Compound Library
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Welcome Trust Cancer Drugs
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
60
Molecular Weight
588.18
Hydrogen Bond Acceptors
13
Hydrogen Bond Donors
3
Rotatable Bonds
5
Ring Count
7
Aromatic Ring Count
2
cLogP
1.34
TPSA
160.83
Fraction CSP3
0.55
Chiral centers
10.0
Largest ring
6.0
QED
0.43
Structural alerts
1
Genotoxic
Nuisance compounds
Custom attributes
(extracted from source data)
Target
TOP2A
TOP2
TOP2A, TOP2B
antibiotic
Bacterial
Mitophagy
Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,Autophagy,Mitophagy,Topoisomerase
Topo II
Compound status
FDA
Target Type
Enzymes
Pathway
DNA replication
Apoptosis
Autophagy
DNA Damage/DNA Repair
Microbiology/virology
Anti-infection
Cell Cycle/DNA Damage
Primary Target
DNA Topoisomerases
MOA
Inhibitor
Topoisomerase
Topoisomerase II inhibitor
Tubulin modulator
"Topoisomerase II inhibitor
Tubulin modulator"
Topoisomerase inhibitor
Member status
member
Indication
non-small cell lung cancer (NSCLC)
Cellular injury category
Genotoxin
Therapeutic Class
Anticancer Agents
Nuisance MOA
Genotoxic
Targets
Topoisomerase II
Source data

