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Epirubicin hydrochloride, 98%, a semisynthetic L-arabino derivative of doxorubicin, and an antineoplastic agent by inhibiting Topoisomerase|194237|56390-09-1

Epirubicin hydrochloride, 98%, a semisynthetic L-arabino derivative of doxorubicin, and an antineoplastic agent by inhibiting Topoisomerase

Cat. No JK194237_100_MG
J&K Chemical

Product Information

Product Name
Epirubicin hydrochloride, 98%, a semisynthetic L-arabino derivative of doxorubicin, and an antineoplastic agent by inhibiting Topoisomerase
Brand Name
J&K
Product Number
194237
CAS
56390-09-1
Molecular Formula
C27H29NO11·HCl
Molecular Weight
579.98
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • 4′-Epidoxorubicin hydrochloride
  • Epidoxorubicin hydrochloride
PubChem CID
65348
IUPAC Name
(7S,9S)-7-(2R,4S,5R,6S)-4-amino-5-hydroxy-6-methyloxan-2-yloxy-6,9,11-trihydroxy-9-(2-hydroxyacetyl)-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione;hydrochloride
InChI Key
MWWSFMDVAYGXBV-FGBSZODSSA-N
SMILES
CC@H1C@@H(C@H(CC@@H(O1)OC@H2CC@@(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)CO)O)N)O.Cl

Properties

Melting Point
185
Boiling Point
810.3
Flash Point
443.8
n20D
1.7100
Optical Activity
+274 (C=0.01, Methanol)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H340
H351
H361
Precautionary Statement
P264
P270
P330
P501
P203
P280
P318
P405
P301+P317
Storage Condition
Freezer -20℃

References Data Source From Pubchem

Combined Low-Dose Cetuximab and Green Tea Epigallocatechin-3-Gallate Treatment Induces Lung Cancer Cell Death
Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2025-11
DOI: 10.1007/s11094-025-03462-5

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells
Publication Name: Biochemical and Biophysical Research Communications
Publication Date: 2023-10-30
DOI: 10.1016/j.bbrc.2023.08.050

Biocompatibility of Nanomaterials Reinforced Polymer-Based Nanocomposites
Publication Name: Handbook of Biodegradable Materials
Publication Date: 2023
DOI: 10.1007/978-3-031-09710-2_17

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2
Publication Name: The Journal of biological chemistry
Publication Date: 2022-08
DOI: 10.1016/j.jbc.2022.102228

Indispensable role of microbes in anticancer drugs and discovery trends
Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2022-07-11
DOI: 10.1007/s00253-022-12046-2

Epirubicin hydrochloride, 98%, a semisynthetic L-arabino derivative of doxorubicin, and an antineoplastic agent by inhibiting Topoisomerase

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