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Details

Stereochemistry ABSOLUTE
Molecular Formula C45H57NO14
Molecular Weight 835.9324
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CABAZITAXEL

SMILES

[H][C@@]12C[C@H](OC)[C@@]3(C)C(=O)[C@H](OC)C4=C(C)[C@H](C[C@@](O)([C@@H](OC(=O)C5=CC=CC=C5)[C@]3([H])[C@@]1(CO2)OC(C)=O)C4(C)C)OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C6=CC=CC=C6

InChI

InChIKey=BMQGVNUXMIRLCK-OAGWZNDDSA-N
InChI=1S/C45H57NO14/c1-24-28(57-39(51)33(48)32(26-17-13-11-14-18-26)46-40(52)60-41(3,4)5)22-45(53)37(58-38(50)27-19-15-12-16-20-27)35-43(8,36(49)34(55-10)31(24)42(45,6)7)29(54-9)21-30-44(35,23-56-30)59-25(2)47/h11-20,28-30,32-35,37,48,53H,21-23H2,1-10H3,(H,46,52)/t28-,29-,30+,32-,33+,34+,35-,37-,43+,44-,45+/m0/s1

HIDE SMILES / InChI

Molecular Formula C45H57NO14
Molecular Weight 835.9324
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 11
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:47:11 UTC 2023
Edited
by admin
on Fri Dec 15 16:47:11 UTC 2023
Record UNII
51F690397J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CABAZITAXEL
EMA EPAR   INN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
TXD258
Code English
CABAZITAXEL [MI]
Common Name English
Cabazitaxel [WHO-DD]
Common Name English
NSC-761432
Code English
CABAZITAXEL ACETONATE [JAN]
Common Name English
XRP6258
Code English
CABAZITAXEL [EMA EPAR]
Common Name English
CABAZITAXEL [USAN]
Common Name English
CABAZITAXEL [VANDF]
Common Name English
CABAZITAXEL [MART.]
Common Name English
CABAZITAXEL [ORANGE BOOK]
Common Name English
1-HYDROXY-7.BETA.,10.BETA.-DIMETHOXY-9-OXO-5.BETA.,20-EPOXYTAX-11-ENE-2.ALPHA.,4,13.ALPHA.-TRIYL 4-ACETATE 2-BENZOATE 13-((2R,3S)-3-(((TERT-BUTOXY)CARBONYL)AMINO)-2-HYDROXY-3-PHENYLPROPANOATE)
Common Name English
XRP-6258
Code English
TXD-258
Code English
cabazitaxel [INN]
Common Name English
JEVTANA
Brand Name English
Classification Tree Code System Code
NDF-RT N0000175085
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
NDF-RT N0000175592
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
NCI_THESAURUS C67437
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
WHO-ATC L01CD04
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
EMA ASSESSMENT REPORTS JETVANA (AUTHORIZED: PROSTATIC, NEOPLASMS)
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
NCI_THESAURUS C1490
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
LIVERTOX NBK548533
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
WHO-VATC QL01CD04
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
Code System Code Type Description
MESH
C552428
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
USAN
XX-92
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
DRUG BANK
DB06772
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
SMS_ID
100000115694
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
CAS
183133-96-2
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
DRUG CENTRAL
4153
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
PUBCHEM
9854073
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID40171389
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
RXCUI
996051
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
CABAZITAXEL
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
MERCK INDEX
m2874
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL1201748
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
NSC
761432
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
DAILYMED
51F690397J
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
NCI_THESAURUS
C66937
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
IUPHAR
6798
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
EVMPD
SUB31282
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
CHEBI
63584
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
FDA UNII
51F690397J
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
INN
8967
Created by admin on Fri Dec 15 16:47:11 UTC 2023 , Edited by admin on Fri Dec 15 16:47:11 UTC 2023
PRIMARY
Related Record Type Details
EXCRETED UNCHANGED
URINE
TRANSPORTER -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
As cabazitaxel is mainly metabolized by CYP3A in vitro, strong CYP3A inducers or inhibitors are expected to affect the pharmacokinetics of cabazitaxel.
MAJOR
SOLVATE->ANHYDROUS
SALT/SOLVATE -> PARENT
METABOLIC ENZYME -> SUBSTRATE
MINOR
SALT/SOLVATE -> PARENT
METABOLIC ENZYME -> SUBSTRATE
As cabazitaxel is mainly metabolized by CYP3A in vitro, strong CYP3A inducers or inhibitors are expected to affect the pharmacokinetics of cabazitaxel.
MAJOR
BINDER->LIGAND
BINDING
SOLVATE->ANHYDROUS
EXCRETED UNCHANGED
FECAL
Related Record Type Details
METABOLITE ACTIVE -> PARENT
by the CYP3A4/5 isoenzyme
METABOLITE ACTIVE -> PARENT
by the CYP3A4/5 isoenzyme
METABOLITE -> PARENT
METABOLITE ACTIVE -> PARENT
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
Tmax PHARMACOKINETIC intravenous infusion

blood-to-plasma ratio PHARMACOKINETIC