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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H32N4O4
Molecular Weight 476.5674
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BMS-561392

SMILES

CC(C)C[C@@H](N1CC[C@](N)(C1=O)C2=CC=C(OCC3=CC(C)=NC4=CC=CC=C34)C=C2)C(=O)NO

InChI

InChIKey=QVNZBDLTUKCPGJ-SHQCIBLASA-N
InChI=1S/C27H32N4O4/c1-17(2)14-24(25(32)30-34)31-13-12-27(28,26(31)33)20-8-10-21(11-9-20)35-16-19-15-18(3)29-23-7-5-4-6-22(19)23/h4-11,15,17,24,34H,12-14,16,28H2,1-3H3,(H,30,32)/t24-,27-/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of DPC 333 [(2R)-2-{(3R)-3-amino-3-[4-(2-methylquinolin-4-ylmethoxy)phenyl]-2-oxopyrrolidin-1-yl}-N-hydroxy-4-methylpentanamide], a human tumor necrosis factor alpha-converting enzyme inhibitor, on the disposition of methotrexate: a transporter-based drug-drug interaction case study.
2007 Jun
Role of P-glycoprotein and the intestine in the excretion of DPC 333 [(2R)-2-{(3R)-3-amino-3-[4-(2-methylquinolin-4-ylmethoxy)phenyl]-2-oxopyrrolidin-1-yl}-N-hydroxy-4-methylpentanamide] in rodents.
2008 Jun
Current perspective of TACE inhibitors: a review.
2009 Jan 15
Name Type Language
BMS-561392
Common Name English
DPC-333
Code English
BMS561392
Code English
(2R)-2-((3R)-3-AMINO-3-(4-((2-METHYL-4-QUINOLINYL)METHOXY)PHENYL)-2-OXO-1-PYRROLIDINYL)-N-HYDROXY-4-METHYLPENTANAMIDE
Systematic Name English
Code System Code Type Description
CAS
611227-74-8
Created by admin on Sat Dec 16 09:06:24 GMT 2023 , Edited by admin on Sat Dec 16 09:06:24 GMT 2023
PRIMARY
PUBCHEM
9847838
Created by admin on Sat Dec 16 09:06:24 GMT 2023 , Edited by admin on Sat Dec 16 09:06:24 GMT 2023
PRIMARY
EVMPD
SUB33630
Created by admin on Sat Dec 16 09:06:24 GMT 2023 , Edited by admin on Sat Dec 16 09:06:24 GMT 2023
PRIMARY
SMS_ID
100000127545
Created by admin on Sat Dec 16 09:06:24 GMT 2023 , Edited by admin on Sat Dec 16 09:06:24 GMT 2023
PRIMARY
FDA UNII
2X066A8676
Created by admin on Sat Dec 16 09:06:24 GMT 2023 , Edited by admin on Sat Dec 16 09:06:24 GMT 2023
PRIMARY