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TargetBcl-2-like protein 1
LigandBDBM53267
Substrate/Competitorn/a
Meas. Tech.Counterscreen for inhibitors of MCL1: fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of BCL2-related protein, long isoform (BCLXL).
IC50 103947±n/a nM
Citation PubChem, PC Counterscreen for inhibitors of MCL1: fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of BCL2-related protein, long isoform (BCLXL). PubChem Bioassay(2009)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Bcl-2-like protein 1
Name:Bcl-2-like protein 1
Synonyms:Anti-apoptotic Bcl-2 protein | Apoptosis Regulator Bcl-xL | Apoptosis regulator Bcl-X | B2CL1_HUMAN | BCL2-like 1 isoform 1 | BCL2L | BCL2L1 | BCLX | Bcl-2-like protein 1 (Bcl-XL) | Bcl-X | Bcl-xL/Bcl-2-binding component 3 | Bcl2-L-1 | Bcl2-antagonist of cell death (BAD)
Type:Mitochondrion membrane; Single-pass membrane protein
Mol. Mass.:26039.60
Organism:Homo sapiens (Human)
Description:n/a
Residue:233
Sequence:
MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLA
DSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAY
QSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEP
WIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK
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BDBM53267
n/a
NameBDBM53267
Synonyms:4-[2-[(E)-[2,4-bis(oxidanylidene)-3-(2-oxidanylidene-2-pyrrolidin-1-yl-ethyl)-1,3-thiazolidin-5-ylidene]methyl]pyrrol-1-yl]benzoic acid | 4-[2-[(E)-[2,4-diketo-3-(2-keto-2-pyrrolidino-ethyl)thiazolidin-5-ylidene]methyl]pyrrol-1-yl]benzoic acid | 4-[2-[(E)-[2,4-dioxo-3-(2-oxo-2-pyrrolidin-1-ylethyl)-1,3-thiazolidin-5-ylidene]methyl]pyrrol-1-yl]benzoic acid | 4-[2-[(E)-[2,4-dioxo-3-[2-oxo-2-(1-pyrrolidinyl)ethyl]-5-thiazolidinylidene]methyl]-1-pyrrolyl]benzoic acid | 4-{2-[2,4-Dioxo-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)-thiazolidin-(5E)-ylidenemethyl]-pyrrol-1-yl}-benzoic acid | MLS001219090 | SMR000605630 | cid_6490291
TypeSmall organic molecule
Emp. Form.C21H19N3O5S
Mol. Mass.425.458
SMILESOC(=O)c1ccc(cc1)-n1cccc1\C=C1\SC(=O)N(CC(=O)N2CCCC2)C1=O
Structure
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