Compile Data Set for Download or QSAR

Found 21 hits with Last Name = 'baizman' and Initial = 'er'   

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
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229939 (CHEMBL423481) Show SMILES [H][C@@](C)(CCCc1ccccc1)Oc1cc(O)c2c(N[C@@H](C)[C@]3([H])CC[C@@H](O)C[C@@]23[H])c1 Show InChI InChI=1S/C25H33NO3/c1-16(7-6-10-18-8-4-3-5-9-18)29-20-14-23-25(24(28)15-20)22-13-19(27)11-12-21(22)17(2)26-23/h3-5,8-9,14-17,19,21-22,26-28H,6-7,10-13H2,1-2H3/t16-,17+,19-,21+,22-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.460	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229940 (CHEMBL286248) Show SMILES Cc1c(C(=O)c2ccc(Br)c3ccccc23)c2cccc3OCC(CN4CCOCC4)n1c23 Show InChI InChI=1S/C27H25BrN2O3/c1-17-25(27(31)21-9-10-23(28)20-6-3-2-5-19(20)21)22-7-4-8-24-26(22)30(17)18(16-33-24)15-29-11-13-32-14-12-29/h2-10,18H,11-16H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.30	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM21281 ((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...) Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r| Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	5.56	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM21281 ((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...) Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r| Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	5.60	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229943 (CHEMBL27388) Show SMILES O=C(c1cn2C(CN3CCOCC3)COc3cccc1c23)c1cccc2ccccc12 Show InChI InChI=1S/C26H24N2O3/c29-26(22-9-3-6-18-5-1-2-7-20(18)22)23-16-28-19(15-27-11-13-30-14-12-27)17-31-24-10-4-8-21(23)25(24)28/h1-10,16,19H,11-15,17H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	7.40	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229941 (CHEMBL1744071) Show SMILES Cc1c(C(=O)c2cccc3c(Br)cc(Br)cc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r| Show InChI InChI=1S/C27H24Br2N2O3/c1-16-25(27(32)20-5-2-4-19-22(20)12-17(28)13-23(19)29)21-6-3-7-24-26(21)31(16)18(15-34-24)14-30-8-10-33-11-9-30/h2-7,12-13,18H,8-11,14-15H2,1H3/t18-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229942 (CHEMBL343532) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n2[C@H](CN3CCOCC3)COc3cccc1c23 Show InChI InChI=1S/C24H26N2O4/c1-16-22(24(27)17-6-8-19(28-2)9-7-17)20-4-3-5-21-23(20)26(16)18(15-30-21)14-25-10-12-29-13-11-25/h3-9,18H,10-15H2,1-2H3/t18-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	106	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229935 (CHEMBL284678) Show SMILES Cc1c(C(=O)c2ccc3ncccc3c2)c2cccc3OCC(CN4CCOCC4)n1c23 Show InChI InChI=1S/C26H25N3O3/c1-17-24(26(30)19-7-8-22-18(14-19)4-3-9-27-22)21-5-2-6-23-25(21)29(17)20(16-32-23)15-28-10-12-31-13-11-28/h2-9,14,20H,10-13,15-16H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	133	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229934 (CHEMBL440651) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n2C(CN3CCOCC3)COc3cccc1c23 Show InChI InChI=1S/C24H26N2O4/c1-16-22(24(27)17-6-8-19(28-2)9-7-17)20-4-3-5-21-23(20)26(16)18(15-30-21)14-25-10-12-29-13-11-25/h3-9,18H,10-15H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	152	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229944 (CHEMBL25847) Show SMILES COc1ccc(cc1)C(=O)c1cn2C(CN3CCOCC3)COc3cccc1c23 Show InChI InChI=1S/C23H24N2O4/c1-27-18-7-5-16(6-8-18)23(26)20-14-25-17(13-24-9-11-28-12-10-24)15-29-21-4-2-3-19(20)22(21)25/h2-8,14,17H,9-13,15H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	249	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229937 (CHEMBL280991) Show SMILES Cc1c(C(=O)c2ccccc2F)c2cccc3OCC(CN4CCOCC4)n1c23 Show InChI InChI=1S/C23H23FN2O3/c1-15-21(23(27)17-5-2-3-7-19(17)24)18-6-4-8-20-22(18)26(15)16(14-29-20)13-25-9-11-28-12-10-25/h2-8,16H,9-14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.43E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50218278 (CHEMBL279571) Show SMILES CCCCCCCCCCCCO[C@H](COP(O)(=O)OC1OC(C(O)C(NC(=O)Nc2ccc(Cl)c(c2)C(F)(F)F)C1OC1OC(CO)C(O)C(O)C1NC(=O)c1cccc(c1)C(F)(F)F)C(N)=O)C(O)=O Show InChI InChI=1S/C43H58ClF6N4O17P/c1-2-3-4-5-6-7-8-9-10-11-17-66-28(38(61)62)21-67-72(64,65)71-40-34(29(33(58)35(70-40)36(51)59)54-41(63)52-24-15-16-26(44)25(19-24)43(48,49)50)69-39-30(32(57)31(56)27(20-55)68-39)53-37(60)22-13-12-14-23(18-22)42(45,46)47/h12-16,18-19,27-35,39-40,55-58H,2-11,17,20-21H2,1H3,(H2,51,59)(H,53,60)(H,61,62)(H,64,65)(H2,52,54,63)/t27?,28-,29?,30?,31?,32?,33?,34?,35?,39?,40?/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50335519 ((S)-3,6-Diamino-hexanoic acid {(3S,9S,12S,15S)-3-(...) Show SMILES CN[C@H](CC(C)C)C(=O)N[C@@H]1[C@H](O)c2ccc(Oc3cc4cc(Oc5ccc(cc5Cl)[C@@H](O)[C@@H]5NC(=O)[C@H](NC(=O)[C@@H]4NC(=O)[C@H](CC(N)=O)NC1=O)c1ccc(O)c(c1)-c1c(O)cc(O)cc1[C@H](NC5=O)C(O)=O)c3O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1)c(Cl)c2 |r| Show InChI InChI=1S/C66H75Cl2N9O24/c1-23(2)12-34(71-5)58(88)76-49-51(83)26-7-10-38(32(67)14-26)97-40-16-28-17-41(55(40)101-65-56(54(86)53(85)42(22-78)99-65)100-44-21-66(4,70)57(87)24(3)96-44)98-39-11-8-27(15-33(39)68)52(84)50-63(93)75-48(64(94)95)31-18-29(79)19-37(81)45(31)30-13-25(6-9-36(30)80)46(60(90)77-50)74-61(91)47(28)73-59(89)35(20-43(69)82)72-62(49)92/h6-11,13-19,23-24,34-35,42,44,46-54,56-57,65,71,78-81,83-87H,12,20-22,70H2,1-5H3,(H2,69,82)(H,72,92)(H,73,89)(H,74,91)(H,75,93)(H,76,88)(H,77,90)(H,94,95)/t24-,34+,35-,42+,44-,46+,47+,48-,49+,50-,51+,52+,53+,54-,56+,57+,65-,66-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50008022 ((4-Methoxy-phenyl)-(3-morpholin-4-ylmethyl-2,3-dih...) Show SMILES COc1ccc(cc1)C(=O)c1c2CCC(CN3CCOCC3)n2c2ccccc12 Show InChI InChI=1S/C24H26N2O3/c1-28-19-9-6-17(7-10-19)24(27)23-20-4-2-3-5-21(20)26-18(8-11-22(23)26)16-25-12-14-29-15-13-25/h2-7,9-10,18H,8,11-16H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	3.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50008029 ((4-Methoxy-phenyl)-[2-methyl-1-(2-morpholin-4-yl-e...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2ccccc12 Show InChI InChI=1S/C23H26N2O3/c1-17-22(23(26)18-7-9-19(27-2)10-8-18)20-5-3-4-6-21(20)25(17)12-11-24-13-15-28-16-14-24/h3-10H,11-16H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229938 (CHEMBL1592888) Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@H](CN4CCOCC4)n1c23 Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1/2 (Rattus norvegicus (Rat)-Rattus norvegicus (rat))	BDBM50229936 (CHEMBL1788279) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n2[C@@H](CN3CCOCC3)COc3cccc1c23 |r| Show InChI InChI=1S/C24H26N2O4/c1-16-22(24(27)17-6-8-19(28-2)9-7-17)20-4-3-5-21-23(20)26(16)18(15-30-21)14-25-10-12-29-13-11-25/h3-9,18H,10-15H2,1-2H3/t18-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.75E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Research Group Curated by ChEMBL					Assay Description Concentration required to displace 50% of 0.5 nM [3H](aminoalkyl)indole binding to cannabinoid receptor in rat cerebellum membranes				J Med Chem 35: 124-35 (1992) BindingDB Entry DOI: 10.7270/Q2SF2ZDZ
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50218323 (CHEMBL406969) Show SMILES CC(C)CCCC(C)CCC(C)CCC(C)(C)CCCCC(C)CCO[C@H](COP(O)(=O)OC1OC(C(N)=O)C(C)(O)C(OC(N)=O)C1OC1OC(CO)C(OC2OC(C)C(O)C(O)C2NC(C)=O)C(O)C1NC(C)=O)C(O)=O Show InChI InChI=1S/C52H95N4O22P/c1-27(2)15-14-17-28(3)18-19-30(5)20-23-51(9,10)22-13-12-16-29(4)21-24-70-35(46(64)65)26-71-79(68,69)78-49-42(43(77-50(54)66)52(11,67)44(76-49)45(53)63)75-48-37(56-33(8)59)40(62)41(34(25-57)73-48)74-47-36(55-32(7)58)39(61)38(60)31(6)72-47/h27-31,34-44,47-49,57,60-62,67H,12-26H2,1-11H3,(H2,53,63)(H2,54,66)(H,55,58)(H,56,59)(H,64,65)(H,68,69)/t28?,29?,30?,31?,34?,35-,36?,37?,38?,39?,40?,41?,42?,43?,44?,47?,48?,49?,52?/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50218322 (CHEMBL2029021) Show SMILES CC(C)CCCC(C)CCC(C)CCC(C)(C)CCCCC(C)CCO[C@H](COP(O)(=O)O[C@H]1O[C@@H](C(N)=O)[C@@](C)(O)[C@H](OC(N)=O)[C@@H]1O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H](O[C@@H]2O[C@@H](C)[C@@H](O[C@@H]3O[C@H]([C@H](O)[C@H](O)[C@@H]3O)C(N)=O)[C@H](O)[C@@H]2NC(C)=O)[C@@H](O)[C@@H]1NC(C)=O)C(O)=O Show InChI InChI=1S/C64H114N5O32P/c1-28(2)15-14-17-29(3)18-19-31(5)20-23-63(9,10)22-13-12-16-30(4)21-24-89-37(56(83)84)27-91-102(87,88)101-61-51(52(100-62(67)85)64(11,86)53(99-61)55(66)82)98-58-39(69-34(8)72)42(75)49(36(94-58)26-90-59-46(79)43(76)40(73)35(25-70)93-59)96-57-38(68-33(7)71)41(74)48(32(6)92-57)95-60-47(80)44(77)45(78)50(97-60)54(65)81/h28-32,35-53,57-61,70,73-80,86H,12-27H2,1-11H3,(H2,65,81)(H2,66,82)(H2,67,85)(H,68,71)(H,69,72)(H,83,84)(H,87,88)/t29?,30?,31?,32-,35-,36-,37+,38-,39-,40+,41+,42-,43-,44-,45+,46-,47-,48+,49+,50+,51-,52+,53-,57-,58-,59+,60+,61+,64-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>7.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50218324 (CHEMBL2029019) Show SMILES CC(C)CCCC(C)CCC(C)CCC(C)(C)CCCCC(C)CCO[C@H](COP(O)(=O)O[C@H]1O[C@@H](C(N)=O)[C@@](C)(O)[C@H](OC(N)=O)C1O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H](O[C@@H]2O[C@@H](C)[C@@H](O[C@@H]3O[C@H]([C@H](O)[C@H](O)[C@@H]3O)C(=O)NC3=C(O)CCC3=O)[C@H](O)[C@@H]2NC(C)=O)[C@@H](O)[C@@H]1NC(C)=O)C(O)=O |c:88| Show InChI InChI=1S/C69H118N5O34P/c1-30(2)15-14-17-31(3)18-19-33(5)22-25-68(9,10)24-13-12-16-32(4)23-26-96-41(61(90)91)29-98-109(94,95)108-66-56(57(107-67(71)92)69(11,93)58(106-66)59(70)88)105-63-44(73-36(8)77)47(82)54(40(101-63)28-97-64-51(86)48(83)45(80)39(27-75)100-64)103-62-43(72-35(7)76)46(81)53(34(6)99-62)102-65-52(87)49(84)50(85)55(104-65)60(89)74-42-37(78)20-21-38(42)79/h30-34,39-41,43-58,62-66,75,78,80-87,93H,12-29H2,1-11H3,(H2,70,88)(H2,71,92)(H,72,76)(H,73,77)(H,74,89)(H,90,91)(H,94,95)/t31?,32?,33?,34-,39-,40-,41+,43-,44-,45+,46+,47-,48-,49-,50+,51-,52-,53+,54+,55+,56?,57+,58-,62-,63-,64+,65+,66+,69-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>7.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50218279 (MOENOMYCIN) Show SMILES [#6]-[#6@@H]-1-[#8]-[#6@@H](-[#8]-[#6@H]-2-[#6@@H](-[#8])-[#6@H](-[#7]-[#6](-[#6])=O)-[#6@H](-[#8]-[#6@@H]-3-[#6@@H](-[#8]P([#8])(=O)[#8]-[#6]-[#6@@H](-[#8]-[#6]\[#6]=[#6](\[#6])-[#6]-[#6]\[#6]=[#6]\C([#6])([#6])[#6]-[#6]-[#6](=[#6])-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](/[#6])-[#6])-[#6](-[#8])=O)-[#8]-[#6@@H](-[#6](-[#7])=O)[C@@]([#6])([#8])[#6@@H]-3-[#8]-[#6](-[#7])=O)-[#8]-[#6@H]-2-[#6]-[#8]-[#6@@H]-2-[#8]-[#6@@H](-[#6]-[#8])-[#6@@H](-[#8])-[#6@H](-[#8])-[#6@@H]-2-[#8])-[#6@@H](-[#7]-[#6](-[#6])=O)-[#6@@H](-[#8])-[#6@@H]-1-[#8]-[#6@@H]-1-[#8]-[#6@H](-[#6@H](-[#8])-[#6@H](-[#8])-[#6@@H]-1-[#8])-[#6](=O)-[#7]-[#6]-1=[#6](-[#8])-[#6]-[#6]-[#6]-1=O |c:107| Show InChI InChI=1S/C69H108N5O34P/c1-30(2)15-14-17-31(3)18-19-33(5)22-25-68(9,10)24-13-12-16-32(4)23-26-96-41(61(90)91)29-98-109(94,95)108-66-56(57(107-67(71)92)69(11,93)58(106-66)59(70)88)105-63-44(73-36(8)77)47(82)54(40(101-63)28-97-64-51(86)48(83)45(80)39(27-75)100-64)103-62-43(72-35(7)76)46(81)53(34(6)99-62)102-65-52(87)49(84)50(85)55(104-65)60(89)74-42-37(78)20-21-38(42)79/h13,15,18,23-24,34,39-41,43-58,62-66,75,78,80-87,93H,5,12,14,16-17,19-22,25-29H2,1-4,6-11H3,(H2,70,88)(H2,71,92)(H,72,76)(H,73,77)(H,74,89)(H,90,91)(H,94,95)/b24-13+,31-18+,32-23-/t34-,39-,40-,41+,43-,44-,45+,46+,47-,48-,49-,50+,51-,52-,53+,54+,55+,56-,57+,58-,62-,63-,64+,65+,66+,69-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>7.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Advanced Medicine, Inc. Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptidoglycan synthesis in Enterococcus faecalis using [14C]lysine radioligand				Bioorg Med Chem Lett 10: 2251-4 (2000) BindingDB Entry DOI: 10.7270/Q2D79DM6
					More data for this Ligand-Target Pair