Compile Data Set for Download or QSAR

Found 254 hits Enz. Inhib. hit(s) with Target = 'Bcl-2-like protein 1 [1-212]'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577683 (US11478451, Example 087 | US11478451, Example 088 ...) Show SMILES Cc1c-2c(COCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577720 ((rac)-4-Chloro-3-ethyl-12,12-difluoro-7-{3-[(6-flu...) Show SMILES CCc1c-2c(CN(C)CC(F)(F)CCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577692 (US11478451, Example 096 | US11478451, Example 097 ...) Show SMILES CCc1c-2c(COCCC(F)(F)Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572210 ((9aS,11 aR)-3-chloro-4,5-dimethyl-15-{3-[(naphthal...) Show SMILES Cc1c-2c(COCC3CCC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571489 ((+)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1-y...) Show SMILES CCc1c-2c(nn1C)C(CC(C)(C)O)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572210 ((9aS,11 aR)-3-chloro-4,5-dimethyl-15-{3-[(naphthal...) Show SMILES Cc1c-2c(COCC3CCC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577692 (US11478451, Example 096 | US11478451, Example 097 ...) Show SMILES CCc1c-2c(COCCC(F)(F)Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572180 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1nn(C)c2COCCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c(-c12)c34 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577683 (US11478451, Example 087 | US11478451, Example 088 ...) Show SMILES Cc1c-2c(COCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571480 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CCO)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572202 ((rac)-4-chloro-12,12-difluoro-2,3-dimethyl-7-{3-[(...) Show SMILES CCc1c-2c(COCC(F)(F)CCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577664 ((rac)-4-chloro-11,11-difluoro-2,3-dimethyl-7-[3-(1...) Show SMILES Cc1c-2c(COCCC(F)(F)Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572210 ((9aS,11 aR)-3-chloro-4,5-dimethyl-15-{3-[(naphthal...) Show SMILES Cc1c-2c(COCC3CCC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577689 (US11478451, Example 093) Show SMILES Cc1c-2c(COCCC(F)(F)Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571527 ((rac)-(rac-15)-benzyl-4-chloro-3-ethyl-7-{3-[(6-fl...) Show SMILES CCc1c-2c(nn1C)C(Cc1ccccc1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.32E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571510 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CCC(C)(C)O)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.33E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571472 ((−)-4-chloro-15-cyclopropyl-2,3-dimethyl-7-{...) Show SMILES Cc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577686 (US11478451, Example 090 | US11478451, Example 091 ...) Show SMILES Cc1c-2c(COCC(F)(F)CCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577698 ((rac)-3-chloro-4-ethyl-14-{3-[(6-fluoronaphthalen-...) Show SMILES CCc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572205 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(CN(CC(F)(F)F)CCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571465 ((+)-4-chloro-15-ethyl-2,3-dimethyl-7-{3-[(naphthal...) Show SMILES CCC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571490 ((−)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthal...) Show SMILES CCc1c-2c(nn1C)C(CC(C)(C)O)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571488 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CC(C)(C)O)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571478 ((+)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1-y...) Show SMILES CCc1c-2c(nn1C)C(CCOC)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572210 ((9aS,11 aR)-3-chloro-4,5-dimethyl-15-{3-[(naphthal...) Show SMILES Cc1c-2c(COCC3CCC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572166 ((rac)-4-chloro-3-ethyl-2-methyl-7-[3-(naphthalen-1...) Show SMILES CCc1c-2c(COCCCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577701 ((rac)-3-chloro-4-ethyl-14-{3-[(6-fluoronaphthalen-...) Show SMILES CCc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571477 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CCOC)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577664 ((rac)-4-chloro-11,11-difluoro-2,3-dimethyl-7-[3-(1...) Show SMILES Cc1c-2c(COCCC(F)(F)Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571496 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CCC1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572205 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(CN(CC(F)(F)F)CCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577706 ((+)-4′-chloro-3′-ethyl-7′-{3-[(6...) Show SMILES CCc1c-2c(COCC3(CC3)CCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572149 (US11447504, Example 2 | US11447504, Example 3 | US...) Show SMILES Cc1nn(C)c2COCCCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c(-c12)c34 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577705 ((−)-4′-chloro-3′-ethyl-7′-...) Show SMILES CCc1c-2c(COCC3(CC3)CCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577700 ((−)-3-chloro-4-ethyl-14-{3-[(6-fluoronaphtha...) Show SMILES CCc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572212 ((9aS,10aR or 9aR, 10aS)-3-chloro-4,5-dimethyl-14-{...) Show SMILES Cc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572183 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(COCCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571473 ((rac)-4-chloro-(15-rac)-(2-methoxyethyl)-2,3-dimet...) Show SMILES COCCC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.71E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571479 ((−)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthal...) Show SMILES CCc1c-2c(nn1C)C(CCOC)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.72E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572180 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1nn(C)c2COCCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c(-c12)c34 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577683 (US11478451, Example 087 | US11478451, Example 088 ...) Show SMILES Cc1c-2c(COCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572212 ((9aS,10aR or 9aR, 10aS)-3-chloro-4,5-dimethyl-14-{...) Show SMILES Cc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571475 ((+)-4-chloro-15-cyclopropyl-3-ethyl-7-{3-[(6-fluor...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.81E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM577659 ((rac)-4-chloro-14-(2,2-difluoroethyl)-3-ethyl-7-{3...) Show SMILES CCc1c-2c(CN(CC(F)F)CCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572212 ((9aS,10aR or 9aR, 10aS)-3-chloro-4,5-dimethyl-14-{...) Show SMILES Cc1c-2c(COCC3CC3Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572205 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(CN(CC(F)(F)F)CCCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NG4TXW
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571464 ((rac)-4-Chloro-15-cyclopropyl-2,3-dimethyl-7-{3-[(...) Show SMILES Cc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.98E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-XL and the BH3 domain of Bad (both human) w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212] (Homo sapiens (Human))	BDBM544459 ((rac)-(11Z)-4-fluoro-2,3-dimethyl-7-[3-(naphthalen...) Show SMILES Cc1c-2c(COC\C=C/Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(F)c-2c34)nn1C |c:7| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description BCL-XL Assay: In the assay 11 different concentrations of each compound (0.1 nM, 0.33 nM, 1.1 nM, 3.8 nM, 13 nM, 44 nM, 0.15 μM, 0.51 μM, 1...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WW7MWD
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212] (Homo sapiens (Human))	BDBM544460 ((rac)-4-fluoro-2,3-dimethyl-7-[3-(naphthalen-1-ylo...) Show SMILES Cc1c-2c(COCCCCn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(F)c-2c34)nn1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description BCL-XL Assay: In the assay 11 different concentrations of each compound (0.1 nM, 0.33 nM, 1.1 nM, 3.8 nM, 13 nM, 44 nM, 0.15 μM, 0.51 μM, 1...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WW7MWD
					More data for this Ligand-Target Pair
Bcl-2-like protein 1 [1-212] (Homo sapiens (Human))	BDBM544464 ((rac)-(11Z)-3-ethyl-4-fluoro-2-methyl-7-[3-(naphth...) Show SMILES CCc1c-2c(COC\C=C/Cn3c(C(O)=O)c(CCCOc4cccc5ccccc45)c4ccc(F)c-2c34)nn1C |c:8| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description BCL-XL Assay: In the assay 11 different concentrations of each compound (0.1 nM, 0.33 nM, 1.1 nM, 3.8 nM, 13 nM, 44 nM, 0.15 μM, 0.51 μM, 1...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WW7MWD
					More data for this Ligand-Target Pair

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