Esorubicin hydrochloride
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Esorubicin hydrochloride
structure -
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CAS No:
63950-06-1
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Formula:
C27H29NO10.ClH
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Chemical Name:
Esorubicin hydrochloride
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Synonyms:
5,12-Naphthacenedione,10-[[(2S,4R,6S)-4-aminotetrahydro-6-methyl-2H-pyran-2-yl]oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-,hydrochloride (1:1),(8S,10S)-;5,12-Naphthacenedione,10-[(4-aminotetrahydro-6-methyl-2H-pyran-2-yl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-,hydrochloride,[2S-[2α(8R*,10R*),4β,6β]]-;5,12-Naphthacenedione,10-[[(2S,4R,6S)-4-aminotetrahydro-6-methyl-2H-pyran-2-yl]oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-,hydrochloride,(8S,10S)-;4′-Deoxydoxorubicin hydrochloride;Esorubicin hydrochloride;Escorubicin hydrochloride;NSC 267469;IMI 58
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CAS No:
Description
Esorubicin Hydrochloride is a hydrochloride salt of esorubicin, a derivative of the anthracycline antineoplastic antibiotic doxorubicin, with potential antineoplastic activity. Esorubicin intercalates into DNA and inhibits topoisomerase II, thereby inhibiting DNA replication and ultimately, interfering with RNA and protein synthesis. This agent exhibits less cardiotoxicity than the parent antibiotic doxorubicin, but may cause more severe myelosupression compared to other compounds within the anthracycline class.
Esorubicin hydrochloride Basic Attributes
563.98100
563.1558238 g/mol
264-575-1
2UB1JJT82D
DTXSID90213783
C74943
Drug Information
Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. (See all compounds classified as Antibiotics, Antineoplastic.)
4'-deoxyadriamycin
Computed Properties
Molecular Weight:564.0
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:5
Exact Mass:563.1558238
Monoisotopic Mass:563.1558238
Topological Polar Surface Area:186
Heavy Atom Count:39
Complexity:945
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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