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Details

Stereochemistry ABSOLUTE
Molecular Formula C47H51NO15
Molecular Weight 869.9055
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BMS-188797

SMILES

[H][C@]12[C@H](OC(=O)C3=CC=CC=C3)[C@]4(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)C5=CC=CC=C5)C6=CC=CC=C6)C(C)=C([C@@H](OC(C)=O)C(=O)[C@]1(C)[C@@H](O)C[C@H]7OC[C@@]27OC(=O)OC)C4(C)C

InChI

InChIKey=GMJWGJSDPOAZTP-MIDYMNAOSA-N
InChI=1S/C47H51NO15/c1-25-30(61-42(55)35(51)34(27-16-10-7-11-17-27)48-40(53)28-18-12-8-13-19-28)23-47(57)39(62-41(54)29-20-14-9-15-21-29)37-45(5,38(52)36(60-26(2)49)33(25)44(47,3)4)31(50)22-32-46(37,24-59-32)63-43(56)58-6/h7-21,30-32,34-37,39,50-51,57H,22-24H2,1-6H3,(H,48,53)/t30-,31-,32+,34-,35+,36+,37-,39-,45+,46-,47+/m0/s1

HIDE SMILES / InChI

Molecular Formula C47H51NO15
Molecular Weight 869.9055
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 11
E/Z Centers 0
Optical Activity UNSPECIFIED

Bristol-Myers Squibb developed BMS-188797 for the potential treatment of solid tumors. BMS-188797 causes G2/M cell cycle arrest and exhibits potent antiproliferative activity against human tumor cell. BMS-188797 in combination with cisplatin successfully has passed phase I clinical and has been recommended for further phase II trials. However, further development has been halted.

Approval Year

PubMed

PubMed

TitleDatePubMed
Preclinical antitumor activity of two novel taxanes.
2001
The novel taxane analogs, BMS-184476 and BMS-188797, potentiate the effects of radiation therapy in vitro and in vivo against human lung cancer cells.
2001 Oct 1
A phase I and pharmacokinetic study of novel taxane BMS-188797 and cisplatin in patients with advanced solid tumours.
2006 Jan 16
Patents

Sample Use Guides

a fixed dose of carboplatin was combined with a dose escalation schedule of BMS-188797 ( 100, 125, 150, and 175 mg/m2 ), both administered once every 3 weeks, in patients with advanced solid malignancies.
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:51 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:51 GMT 2023
Record UNII
0HG7S0S581
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BMS-188797
Common Name English
4-Desacetylpaclitaxel 4-methyl carbonate [WHO-DD]
Common Name English
4-DESACETYLPACLITAXEL 4-METHYL CARBONATE
WHO-DD  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1490
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
NCI_THESAURUS C67437
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
Code System Code Type Description
DRUG BANK
DB12619
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY
NCI_THESAURUS
C1859
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID50169318
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY
CAS
172481-83-3
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY
PUBCHEM
6918494
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY
FDA UNII
0HG7S0S581
Created by admin on Fri Dec 15 15:43:51 GMT 2023 , Edited by admin on Fri Dec 15 15:43:51 GMT 2023
PRIMARY