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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H33ClN2O5S.ClH
Molecular Weight 461.444
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLINDAMYCIN HYDROCHLORIDE

SMILES

Cl.[H][C@@](NC(=O)[C@@H]1C[C@@H](CCC)CN1C)([C@H](C)Cl)[C@@]2([H])O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O

InChI

InChIKey=AUODDLQVRAJAJM-XJQDNNTCSA-N
InChI=1S/C18H33ClN2O5S.ClH/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
CLINDAMYCIN HYDROCHLORIDE
EP   GREEN BOOK   MART.   MI   ORANGE BOOK   USP   VANDF   WHO-DD  
Common Name English
ANTIROBE
Brand Name English
SOBELIN
Brand Name English
CLINDAMYCIN HYDROCHLORIDE [USP-RS]
Common Name English
CLINDAMYCIN HCL
Common Name English
CLINDAMYCIN HYDROCHLORIDE [GREEN BOOK]
Common Name English
NSC-756696
Code English
DALACIN C
Brand Name English
L-THREO-.ALPHA.-D-GALACTO-OCTOPYRANOSIDE, METHYL 7-CHLORO-6,7,8-TRIDEOXY-6-(((1-METHYL-4-PROPYL-2-PYRROLIDINYL)CARBONYL)AMINO)-1-THIO-,(2S-TRANS)-, MONOHYDROCHLORIDE
Common Name English
CLINDAMYCIN HYDROCHLORIDE [VANDF]
Common Name English
CLINSOL
Brand Name English
CLINTABS
Brand Name English
CLINDAMYCIN HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
CLINDAMYCIN HYDROCHLORIDE [ORANGE BOOK]
Common Name English
CLINDAMYCIN HYDROCHLORIDE [MI]
Common Name English
CLINDAMYCIN HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
CLINDAMYCIN HYDROCHLORIDE [MART.]
Common Name English
CLINDAMYCIN HYDROCHLORIDE [JAN]
Common Name English
CLINDAMYCIN (AS HYDROCHLORIDE)
Common Name English
CLINDAMYCIN HYDROCHLORIDE ANHYDROUS
Common Name English
METHYL 7-CHLORO-6,7,8-TRIDEOXY-6-(1-METHYL-TRANS-4-PROPYL-L-2-PYRROLIDINECARBOXAMIDO)-1-THIO-L-THREO-.ALPHA.-D-GALACTO-OCTOPYRANOSIDE MONOHYDROCHLORIDE
Common Name English
Clindamycin hydrochloride [WHO-DD]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 213405
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
NCI_THESAURUS C82922
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
Code System Code Type Description
CAS
21462-39-5
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
NCI_THESAURUS
C47977
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
EVMPD
SUB127118
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
PUBCHEM
16051951
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
RS_ITEM_NUM
1136002
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
FDA UNII
T20OQ1YN1W
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL1753
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
NSC
756696
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
244-398-6
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
RXCUI
81982
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY RxNorm
DAILYMED
T20OQ1YN1W
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
SMS_ID
100000090552
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
EVMPD
SUB01342MIG
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
MERCK INDEX
m3624
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY Merck Index
DRUG BANK
DBSALT001163
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
EPA CompTox
DTXSID4045428
Created by admin on Fri Dec 15 15:04:50 UTC 2023 , Edited by admin on Fri Dec 15 15:04:50 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of CLINDAMYCIN
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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