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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H29NO11.ClH
Molecular Weight 579.98
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOXORUBICIN HYDROCHLORIDE

SMILES

Cl.[H][C@@]1(C[C@H](N)[C@H](O)[C@H](C)O1)O[C@H]2C[C@@](O)(CC3=C(O)C4=C(C(=O)C5=C(OC)C=CC=C5C4=O)C(O)=C23)C(=O)CO

InChI

InChIKey=MWWSFMDVAYGXBV-RUELKSSGSA-N
InChI=1S/C27H29NO11.ClH/c1-10-22(31)13(28)6-17(38-10)39-15-8-27(36,16(30)9-29)7-12-19(15)26(35)21-20(24(12)33)23(32)11-4-3-5-14(37-2)18(11)25(21)34;/h3-5,10,13,15,17,22,29,31,33,35-36H,6-9,28H2,1-2H3;1H/t10-,13-,15-,17-,22+,27-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C27H29NO11
Molecular Weight 543.5193
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:19:48 UTC 2023
Edited
by admin
on Fri Dec 15 15:19:48 UTC 2023
Record UNII
82F2G7BL4E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DOXORUBICIN HYDROCHLORIDE
EMA EPAR   EP   MART.   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
Common Name English
IMX-110 COMPONENT DOXORUBICIN HYDROCHLORIDE
Common Name English
(8S,10S)-10-((3-AMINO-2,3,6-TRIDEOXY-.ALPHA.-L-LYXO-HEXOPYRANOSYL)OXY)-8-GLYCOLOYL-7,8,9,10-TETRAHYDRO-6,8,11-TRIHYDROXY-1-METHOXY-5,12-NAPHTHACENEDIONE HYDROCHLORIDE
Common Name English
ADRIAMYCIN, HYDROCHLORIDE
Common Name English
DOXORUBICIN HYDROCHLORIDE [ORANGE BOOK]
Common Name English
DOXORUBICIN HYDROCHLORIDE [USP-RS]
Common Name English
Doxorubicin hydrochloride [WHO-DD]
Common Name English
DOXORUBICIN HYDROCHLORIDE [EMA EPAR]
Common Name English
CAELYX
Brand Name English
DOXORUBICIN HYDROCHLORIDE LIPOSOME [VANDF]
Common Name English
DOXORUBICINI HYDROCHLORIDUM [WHO-IP LATIN]
Common Name English
DOXORUBICIN HYDROCHLORIDE [MART.]
Common Name English
DOXIL
Brand Name English
DOXORUBICIN HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
DOXORUBICIN HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
HYDROXYDAUNOMYCIN HYDROCHLORIDE
Common Name English
DOXORUBICIN HCL
Common Name English
DOXORUBICIN HYDROCHLORIDE [VANDF]
Common Name English
DOXORUBICIN HYDROCHLORIDE [WHO-IP]
Common Name English
ADRIAMYCIN
Brand Name English
DOXORUBICIN HYDROCHLORIDE LIPOSOME
VANDF  
Common Name English
ADRIABLASTINA CS
Common Name English
ADRIAMYCIN [IARC]
Common Name English
RUBEX
Brand Name English
5,12-NAPHTHACENEDIONE, 10-((3-AMINO-2,3,6-TRIDEOXY-.ALPHA.-L-LYXO-HEXOPYRANOSYL)OXY)-7,8,9,10-TETRAHYDRO-6,8,11-TRIHYDROXY-8-(HYDROXYLACETYL)-1-METHOXY-, HYDROCHLORIDE (8S-CIS)-
Common Name English
Liposomal doxorubicin hydrochloride [WHO-DD]
Common Name English
DOXORUBICIN LIPOSOMAL COMPLEX OF THE HYDROCHLORIDE [MI]
Common Name English
DOXORUBICIN HYDROCHLORIDE [JAN]
Common Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/10/833
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
NCI_THESAURUS C67502
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
EMA ASSESSMENT REPORTS CAELYX (AUTHORIZED: MULTIPLE MYELOMA)
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
EMA ASSESSMENT REPORTS CAELYX (AUTHORIZED: OVARIAN NEOPLASMS)
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
EMA ASSESSMENT REPORTS MYOCET (AUTHORIZED: BREAST NEOLPLASMA)
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
FDA ORPHAN DRUG 229006
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
FDA ORPHAN DRUG 191704
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
FDA ORPHAN DRUG 210705
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
FDA ORPHAN DRUG 628318
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
FDA ORPHAN DRUG 311910
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
246-818-3
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
FDA UNII
82F2G7BL4E
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
CHEBI
28748
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
MERCK INDEX
m4757
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY Merck Index
RXCUI
142433
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
DOXORUBICIN HYDROCHLORIDE
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY Description: A red-orange, crystalline powder. Solubility: Soluble in water and methanol R; practically insoluble in ether R. Category: Cytotoxic drug. Storage: Doxorubicin hydrochloride should be kept in a tightly closed container. Additional information: Doxorubicin hydrochloride is hygroscopic; it is poisonous: CAUTION: Doxorubicin hydrochloride must behandled with care, avoiding contact with the skin and inhalation of airborne particles. Definition. Doxorubicin hydrochloride contains not less than 97.0% and not more than 102.0% of C27H29NO11,HCl, calculatedwith reference to the anhydrous substance.
EVMPD
SUB06391MIG
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
RS_ITEM_NUM
1225703
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
DAILYMED
82F2G7BL4E
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
CAS
25316-40-9
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
PUBCHEM
443939
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
ChEMBL
CHEMBL53463
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
NCI_THESAURUS
C1326
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
RXCUI
466523
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
ALTERNATIVE
EVMPD
SUB01827MIG
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
EVMPD
SUB126795
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
ALTERNATIVE
DRUG BANK
DBSALT000060
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID3030636
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
SMS_ID
100000089971
Created by admin on Fri Dec 15 15:19:48 UTC 2023 , Edited by admin on Fri Dec 15 15:19:48 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
USP
IMPURITY -> PARENT
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY