General
Preferred name
daunorubicin
Synonyms
DAUNORUBICIN HYDROCHLORIDE ()
RP 13057 ()
Rubidomycin ()
Daunorubicin HCl ()
Daunomycin HCl ()
RP-13057 Hydrochloride ()
Rubidomycin hydrochloride ()
Daunorubicin (HCl) ()
RP13057 ()
RP 13057 Hydrochloride ()
RP13057 Hydrochloride ()
Cerubidine ()
Daunorubicin (Hydrochloride) ()
Daunomycin (Hydrochloride) ()
RP 13057 (Hydrochloride) ()
Rubidomycin (Hydrochloride) ()
Daunomycin HCl, Rubidomycin HCl ()
Daunorubicin (RP 13057) HCl ()
DAUNORUBICIN CITRATE ()
FI-6339 HYDROCHLORIDE ()
NSC-82151 ()
NDC 0082-4155 ()
FI 6339 HYDROCHLORIDE ()
NDC-0082-4155 ()
Daunorubicin (as hydrochloride) ()
RP 13057 [AS THE BASE) ()
RP-13057 HYDROCHLORIDE ()
FI 6339 [AS THE BASE] ()
RP 13057 HYDROCHLORIDE ()
Daunorubicine ()
NSC-83142 ()
FI 6339 ()
Daunomycin ()
RP-13057 ()
Daunorubicina ()
FI-6339 ()
Valrubicin impurity, daunorubicin ()
Epirubicin hydrochloride impurity, daunorubicin- ()
Daunoxome ()
Daunorubicin component of vyxeos ()
Daunorubicin liposomal ()
Daunorubicin citrate liposome ()
Daunorubicin-13C-d3 ()
P&D ID
PD009842
CAS
20830-81-3
23541-50-6
11016-72-1
1407-15-4
11006-54-5
Tags
available
nuisance
natural product
drug
Approved by
PMDA
FDA
First approval
1979
1996
Drug indication
Kaposi sarcoma
Acute myeloid leukemia
Neoplasm
Solid tumour/cancer
Acute myeloid leukaemia
Sarcoma
Drug Status
approved
Max Phase
4.0
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 Daunorubicin (Daunomycin) hydrochloride is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin hydrochloride inhibits DNA and RNA synthesis. Daunorubicin hydrochloride is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin hydrochloride is also an anthracycline antibiotic. Daunorubicin hydrochloride can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor[1][2][4][5].
PRICE 53
DESCRIPTION Daunorubicin is an anthracycline class chemotherapeutic for cancer treatment. It has also been shown to potentiate the activity of antibacterial agents of last resort, against multi-drug resistant (MDR) Gram-negative bacteria .
Daunorubicin is on the World Health Organisation's List of Essential Medicines. (GtoPdb)
DESCRIPTION Daunorubicin hydrochloride (Rubidomycin hydrochloride), an anthracycline aminoglycoside antineoplastic, inhibits DNA replication and repair and RNA and protein synthesis. (TargetMol Bioactive Compound Library)
Cell lines
74
Organisms
5
Compound Sets
25
AdooQ Bioactive Compound Library
A10194
Cayman Chemical Bioactives
14159
29101
ChEMBL Approved Drugs
CHEMBL1563
CHEMBL178
CHEMBL1200475
ChEMBL Drugs
CHEMBL1563
CHEMBL178
CHEMBL1200475
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugBank
DB00694
DrugBank Approved Drugs
DB00694
DrugCentral
786
DrugCentral Approved Drugs
786
DrugMAP
DMQUSBT
DrugMAP Approved Drugs
DMQUSBT
EU-OPENSCREEN Bioactive Compound Library
EOS101591
Guide to Pharmacology
7063
LSP-MoA library (Laboratory of Systems Pharmacology)
CHEMBL1563
CHEMBL178
MedChem Express Bioactive Compound Library
HY-13062
NCATS Inxight Approved Drugs
ZS7284E0ZP
NPC Screening Collection
Nuisance compounds in cellular assays
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
daunorubicin-hcl-daunomycin-hcl
TargetMol Bioactive Compound Library
T1511
The Spectrum Collection
ZINC Tool Compounds
ZINC000003917708
External IDs
112
Properties
(calculated by RDKit )
Molecular Weight
527.18
Hydrogen Bond Acceptors
11
Hydrogen Bond Donors
5
Rotatable Bonds
4
Ring Count
5
Aromatic Ring Count
2
cLogP
1.03
TPSA
185.84
Fraction CSP3
0.44
Chiral centers
6.0
Largest ring
6.0
QED
0.31
Structural alerts
3
quinone_A(370)
[!#6&!#1]=[#6]1[#6]=,:[#6][#6](=[!#6&!#1])[#6]=,:[#6]1
PAINS Family A
Intercalation
Nuisance compounds
Optical interference
Fluorescence
Nuisance compounds
Related compounds
Custom attributes
(extracted from source data)
Target
Topoisomerase
ADC Cytotoxin
DNA/RNA Synthesis
Autophagy
TOP2A, TOP2B
ADC Payload
antibiotic
Bacterial
ADC Cytotoxin,Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,COVID-19,DNA/RNA Synthesis,Topoisomerase
DNA synthesis
Pathway
Cell Cycle/DNA Damage
Antibody-drug Conjugate/ADC Related
Apoptosis
Cell Cycle/Checkpoint
DNA Damage/DNA Repair
Microbiology/virology
Anti-infection
Indication
acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL)
MOA
RNA synthesis inhibitor, topoisomerase inhibitor
Therapeutic Class
Anticancer Agents
Source data