Compile Data Set for Download or QSAR

Found 92 hits Enz. Inhib. hit(s) with Target = 'Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide'   

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
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.22E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571495 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13)c1ccccc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.41E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.46E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.51E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.59E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571474 ((rac)-4-chloro-(15-rac)-cyclopropyl-3-ethyl-7-{3-[...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.63E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571469 ((+)-4-chloro-3-ethyl-2-methyl-7-{3-[(naphthalen-1-...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C(F)(F)F Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.63E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572222 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)N(C)CCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2057K58
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571470 ((−)-4-chloro-3-ethyl-2-methyl-7-{3-[(naphtha...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C(F)(F)F Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.78E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571476 ((−)-4-chloro-15-cyclopropyl-3-ethyl-7-{3-[(6...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.83E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571463 ((rac)-4-Chloro-3-ethyl-2-methyl-7-{3-[(naphthalen-...) Show SMILES CCc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C(F)(F)F Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.86E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.88E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2057K58
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572219 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES CN1CCCCCn2c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2057K58
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM572219 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES CN1CCCCCn2c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2057K58
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.93E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.96E+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-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571437 ((rac)-2,3,15-trimethyl-7-[3-(naphthalen-1-yloxy)pr...) Show SMILES CC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3cccc(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571437 ((rac)-2,3,15-trimethyl-7-[3-(naphthalen-1-yloxy)pr...) Show SMILES CC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3cccc(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571437 ((rac)-2,3,15-trimethyl-7-[3-(naphthalen-1-yloxy)pr...) Show SMILES CC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3cccc(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571440 ((rac)-2,3-dimethyl-15-[2-(morpholin-4-yl)ethyl]-7-...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3cccc-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571443 ((rac)-4-fluoro-2,3-dimethyl-15-[2-(morpholin-4-yl)...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571443 ((rac)-4-fluoro-2,3-dimethyl-15-[2-(morpholin-4-yl)...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571446 ((rac)-3-ethyl-4-fluoro-2-methyl-15-[2-(morpholin-4...) Show SMILES CCc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571446 ((rac)-3-ethyl-4-fluoro-2-methyl-15-[2-(morpholin-4...) Show SMILES CCc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571449 ((rac)-4-chloro-2,3-dimethyl-15-[2-(morpholin-4-yl)...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571449 ((rac)-4-chloro-2,3-dimethyl-15-[2-(morpholin-4-yl)...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571449 ((rac)-4-chloro-2,3-dimethyl-15-[2-(morpholin-4-yl)...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571452 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571452 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571452 ((rac)-4-chloro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571455 ((rac)-4-fluoro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571455 ((rac)-4-fluoro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571455 ((rac)-4-fluoro-7-{3-[(6-fluoronaphthalen-1-yl)oxy]...) Show SMILES Cc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(F)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571458 ((rac)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1...) Show SMILES CCc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571459 ((+)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthalen-1-y...) Show SMILES CCc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571460 ((−)-4-chloro-3-ethyl-7-{3-[(6-fluoronaphthal...) Show SMILES CCc1c-2c(nn1C)C(CCN1CCOCC1)OCCCCn1c(C(O)=O)c(CCCOc3cccc4cc(F)ccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571461 ((rac)-4-chloro-15-ethyl-2,3-dimethyl-7-{3-[(naphth...) Show SMILES CCC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571462 ((rac)-4-chloro-15-(2-hydroxyethyl)-2,3-dimethyl-7-...) Show SMILES Cc1c-2c(nn1C)C(CCO)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571466 ((−)-4-chloro-15-ethyl-2,3-dimethyl-7-{3-[(na...) Show SMILES CCC1OCCCCn2c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c(-c4c(C)n(C)nc14)c23 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571467 ((+)-4-chloro-15-(2-hydroxyethyl)-2,3-dimethyl-7-{3...) Show SMILES Cc1c-2c(nn1C)C(CCO)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571468 ((−)-4-chloro-15-(2-hydroxyethyl)-2,3-dimethy...) Show SMILES Cc1c-2c(nn1C)C(CCO)OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/Bad BH3 Peptide (Homo sapiens (Human))	BDBM571471 ((+)-4-chloro-15-cyclopropyl-2,3-dimethyl-7-{3-[(na...) Show SMILES Cc1c-2c(nn1C)C(OCCCCn1c(C(O)=O)c(CCCOc3cccc4ccccc34)c3ccc(Cl)c-2c13)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair
Apoptosis regulator Bcl-2 [1-211]/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 MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 The dose-dependent inhibition by the compounds described in this invention of the interaction between BCL-2 and the BH3 domain of Bad (both human) wa...				Citation and Details BindingDB Entry DOI: 10.7270/Q2J38WT5
					More data for this Ligand-Target Pair

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