Epirubicin hydrochloride
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Epirubicin hydrochloride
structure -
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CAS No:
56390-09-1
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Formula:
C27H29NO11.ClH
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Chemical Name:
Epirubicin hydrochloride
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Synonyms:
5,12-Naphthacenedione,10-[(3-amino-2,3,6-trideoxy-α-L-arabino-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-,hydrochloride (1:1),(8S,10S)-;5,12-Naphthacenedione,10-[(3-amino-2,3,6-trideoxy-α-L-arabino-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-,hydrochloride,(8S-cis)-;5,12-Naphthacenedione,10-[(3-amino-2,3,6-trideoxy-α-L-arabino-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-,hydrochloride,(8S,10S)-;4′-epi-Adriamycin hydrochloride;4′-Epidoxorubicin hydrochloride;Epirubicin hydrochloride;Farmorubicin;Pharmorubicin;Epidoxorubicin hydrochloride;Ellence
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CAS No:
Description
Epirubicin (hydrochloride) is a semisynthetic L-arabino derivative of doxorubicin, and an antineoplastic agent by inhibiting Topoisomerase.
An anthracycline which is the 4'-epi-isomer of doxorubicin. The compound exerts its antitumor effects by interference with the synthesis and function of DNA.
Characteristics
206
1.50360
red to deep red
1.61g/cm3
185 °C (decomp)
810.3°C at 760 mmHg
443.8℃
1.709
soluble in DMSO to 100mM, or in ethanol to 10mM
Desiccate at +4°C
D20 +274° (c = 0.01 in methanol)
Safety Information
NONH for all modes of transport
3
22-63-62-46-40
36/37/38-45-46
QI9295750
Xn
P201-P280-P301 + P312 + P330-P308 + P313
H302-H340-H350-H360
|Danger|H302 (99.21%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P264, P270, P281, P301+P312, P308+P313, P330, P405, and P501|Aggregated GHS information provided by 127 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Compounds that inhibit the activity of DNA TOPOISOMERASE II. Included in this category are a variety of ANTINEOPLASTIC AGENTS which target the eukaryotic form of topoisomerase II and ANTIBACTERIAL AGENTS which target the prokaryotic form of topoisomerase II. (See all compounds classified as Topoisomerase II Inhibitors.)|Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. (See all compounds classified as Antibiotics, Antineoplastic.)
Adriablastin|4' Epi Adriamycin
Computed Properties
Molecular Weight:580.0
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:5
Exact Mass:579.1507385
Monoisotopic Mass:579.1507385
Topological Polar Surface Area:206
Heavy Atom Count:40
Complexity:977
Defined Atom Stereocenter Count:2
Undefined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Extract from the above information
Registered Holders
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DZD (HEZE) PHARMACEUTICAL CO LTD
Active
United States
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Synbias Pharma.Ltd.
Active
Japan
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Gemini PharmChem Mannheim GmbH
Active
Germany
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