Compile Data Set for Download or QSAR

Found 12 hits with Last Name = 'guichard' and Initial = 'g'   

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
Purine nucleoside phosphorylase (Toxoplasma gondii)	BDBM50200328 ((4S,8R,9aS)-4-benzyl-8-(benzyloxy)-hexahydro-1H-py...) Show SMILES O=C1N[C@@H]2C[C@H](CN2C(=O)[C@H](Cc2ccccc2)N1)OCc1ccccc1 Show InChI InChI=1S/C21H23N3O3/c25-20-18(11-15-7-3-1-4-8-15)22-21(26)23-19-12-17(13-24(19)20)27-14-16-9-5-2-6-10-16/h1-10,17-19H,11-14H2,(H2,22,23,26)/t17-,18+,19+/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of Toxoplasma gondii purine nucleoside phosphorylase				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Tumor necrosis factor receptor superfamily member 5 (Homo sapiens (Human))	BDBM50325995 ((2S,2'S,2''S)-N,N',N''-((4S,4'S,4''S,7S,7'S,7''S)-...) Show SMILES NCCCC[C@H](N)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)NCCCCCC(=O)NCCCC[C@@H]1CNC(=O)C[C@H](CCCCNC(=O)CCCCCNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC[C@H](CCCCNC(=O)CCCCCNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC(=O)C1 |r| Show InChI InChI=1S/C117H176N24O23/c118-55-13-7-25-92(121)109(156)132-74-106(153)136-98(67-80-37-49-89(145)50-38-80)115(162)139-95(64-77-31-43-86(142)44-32-77)112(159)127-61-16-1-4-28-101(148)124-58-19-10-22-83-70-105(152)135-85(24-12-21-60-126-103(150)30-6-3-18-63-129-114(161)97(66-79-35-47-88(144)48-36-79)141-117(164)100(69-82-41-53-91(147)54-42-82)138-108(155)76-134-111(158)94(123)27-9-15-57-120)73-130-84(71-104(151)131-72-83)23-11-20-59-125-102(149)29-5-2-17-62-128-113(160)96(65-78-33-45-87(143)46-34-78)140-116(163)99(68-81-39-51-90(146)52-40-81)137-107(154)75-133-110(157)93(122)26-8-14-56-119/h31-54,83-85,92-100,130,142-147H,1-30,55-76,118-123H2,(H,124,148)(H,125,149)(H,126,150)(H,127,159)(H,128,160)(H,129,161)(H,131,151)(H,132,156)(H,133,157)(H,134,158)(H,135,152)(H,136,153)(H,137,154)(H,138,155)(H,139,162)(H,140,163)(H,141,164)/t83-,84-,85-,92-,93-,94-,95-,96-,97-,98-,99-,100-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Biologie Moléculaire et Cellulaire Curated by ChEMBL					Assay Description Inhibition of recombinant human CD40L:mouse CD8 tail binding to human CD40 by surface plasmon resonance method				Nat Chem Biol 1: 377-82 (2005) BindingDB Entry DOI: 10.7270/Q2WD40SN
					More data for this Ligand-Target Pair
Tumor necrosis factor receptor superfamily member 5 (Homo sapiens (Human))	BDBM50325994 ((2S,2'S,2''S)-N,N',N''-((4S,4'S,4''S,7S,7'S,7''S)-...) Show SMILES C[C@H]1NC(=O)[C@H](CCCCNC(=O)CCCCCNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC(=O)[C@@H](C)NC(=O)[C@H](CCCCNC(=O)CCCCCNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC(=O)[C@@H](C)NC(=O)[C@H](CCCCNC(=O)CCCCCNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC1=O |r| Show InChI InChI=1S/C123H183N27O27/c1-76-109(163)145-95(29-14-23-62-131-104(158)32-8-5-20-65-134-116(170)98(68-80-36-48-86(152)49-37-80)149-122(176)101(71-83-42-54-89(155)55-43-83)143-107(161)74-137-113(167)92(128)26-11-17-59-125)119(173)140-78(3)111(165)147-96(30-15-24-63-132-105(159)33-9-6-21-66-135-117(171)99(69-81-38-50-87(153)51-39-81)150-123(177)102(72-84-44-56-90(156)57-45-84)144-108(162)75-138-114(168)93(129)27-12-18-60-126)120(174)141-77(2)110(164)146-94(118(172)139-76)28-13-22-61-130-103(157)31-7-4-19-64-133-115(169)97(67-79-34-46-85(151)47-35-79)148-121(175)100(70-82-40-52-88(154)53-41-82)142-106(160)73-136-112(166)91(127)25-10-16-58-124/h34-57,76-78,91-102,151-156H,4-33,58-75,124-129H2,1-3H3,(H,130,157)(H,131,158)(H,132,159)(H,133,169)(H,134,170)(H,135,171)(H,136,166)(H,137,167)(H,138,168)(H,139,172)(H,140,173)(H,141,174)(H,142,160)(H,143,161)(H,144,162)(H,145,163)(H,146,164)(H,147,165)(H,148,175)(H,149,176)(H,150,177)/t76-,77-,78-,91+,92+,93+,94+,95+,96+,97+,98+,99+,100+,101+,102+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Biologie Moléculaire et Cellulaire Curated by ChEMBL					Assay Description Inhibition of recombinant human CD40L:mouse CD8 tail binding to human CD40 by surface plasmon resonance method				Nat Chem Biol 1: 377-82 (2005) BindingDB Entry DOI: 10.7270/Q2WD40SN
					More data for this Ligand-Target Pair
Tumor necrosis factor receptor superfamily member 5 (Homo sapiens (Human))	BDBM50325996 (CHEMBL1241019 | N1-((5S,11S,14S,44S,47S,53S)-1,5,5...) Show SMILES NCCCC[C@H](N)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)NCCCCCC(=O)NCCCOCC(COCCCNC(=O)CCCCCNC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@@H](N)CCCCN)(COCCCNC(=O)CCCCCNC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@@H](N)CCCCN)NC(=O)CCC(N)=O |r| Show InChI InChI=1S/C113H169N23O26/c114-51-10-7-19-87(117)104(151)127-69-101(148)130-93(66-78-31-43-84(140)44-32-78)110(157)133-90(63-75-25-37-81(137)38-26-75)107(154)124-54-13-1-4-22-97(144)121-57-16-60-160-72-113(136-100(147)50-49-96(120)143,73-161-61-17-58-122-98(145)23-5-2-14-55-125-108(155)91(64-76-27-39-82(138)40-28-76)134-111(158)94(67-79-33-45-85(141)46-34-79)131-102(149)70-128-105(152)88(118)20-8-11-52-115)74-162-62-18-59-123-99(146)24-6-3-15-56-126-109(156)92(65-77-29-41-83(139)42-30-77)135-112(159)95(68-80-35-47-86(142)48-36-80)132-103(150)71-129-106(153)89(119)21-9-12-53-116/h25-48,87-95,137-142H,1-24,49-74,114-119H2,(H2,120,143)(H,121,144)(H,122,145)(H,123,146)(H,124,154)(H,125,155)(H,126,156)(H,127,151)(H,128,152)(H,129,153)(H,130,148)(H,131,149)(H,132,150)(H,133,157)(H,134,158)(H,135,159)(H,136,147)/t87-,88-,89-,90-,91-,92-,93-,94-,95-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	9.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Biologie Moléculaire et Cellulaire Curated by ChEMBL					Assay Description Inhibition of recombinant human CD40L:mouse CD8 tail binding to human CD40 by surface plasmon resonance method				Nat Chem Biol 1: 377-82 (2005) BindingDB Entry DOI: 10.7270/Q2WD40SN
					More data for this Ligand-Target Pair
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200327 ((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...) Show SMILES CN1CN(C\C=C\C(O)=O)C(=O)N[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C16H19N3O4/c1-18-11-19(9-5-8-14(20)21)16(23)17-13(15(18)22)10-12-6-3-2-4-7-12/h2-8,13H,9-11H2,1H3,(H,17,23)(H,20,21)/b8-5+/t13-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 10 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200326 (((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...) Show SMILES CN1CN(CC(=O)OC(C)(C)C)C(=O)N(CC(=O)OC(C)(C)C)[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C24H35N3O6/c1-23(2,3)32-19(28)14-26-16-25(7)21(30)18(13-17-11-9-8-10-12-17)27(22(26)31)15-20(29)33-24(4,5)6/h8-12,18H,13-16H2,1-7H3/t18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 10 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Phospholipase A2 group V (Homo sapiens (Human))	BDBM50200326 (((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...) Show SMILES CN1CN(CC(=O)OC(C)(C)C)C(=O)N(CC(=O)OC(C)(C)C)[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C24H35N3O6/c1-23(2,3)32-19(28)14-26-16-25(7)21(30)18(13-17-11-9-8-10-12-17)27(22(26)31)15-20(29)33-24(4,5)6/h8-12,18H,13-16H2,1-7H3/t18-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 5 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200325 ((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...) Show SMILES CC(C)[C@@H]1NC(=O)N(CC(=O)OC(C)(C)C)CN(C)C1=O Show InChI InChI=1S/C14H25N3O4/c1-9(2)11-12(19)16(6)8-17(13(20)15-11)7-10(18)21-14(3,4)5/h9,11H,7-8H2,1-6H3,(H,15,20)/t11-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 10 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Phospholipase A2 group V (Homo sapiens (Human))	BDBM50200324 ((4S,7S)-4,7-dibenzyl-5-methyl-1,3,5-triazepane-2,6...) Show SMILES CN1[C@@H](Cc2ccccc2)NC(=O)N[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C19H21N3O2/c1-22-17(13-15-10-6-3-7-11-15)21-19(24)20-16(18(22)23)12-14-8-4-2-5-9-14/h2-11,16-17H,12-13H2,1H3,(H2,20,21,24)/t16-,17-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 5 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Phospholipase A2 group V (Homo sapiens (Human))	BDBM50200325 ((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...) Show SMILES CC(C)[C@@H]1NC(=O)N(CC(=O)OC(C)(C)C)CN(C)C1=O Show InChI InChI=1S/C14H25N3O4/c1-9(2)11-12(19)16(6)8-17(13(20)15-11)7-10(18)21-14(3,4)5/h9,11H,7-8H2,1-6H3,(H,15,20)/t11-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 5 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Phospholipase A2 group V (Homo sapiens (Human))	BDBM50200327 ((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...) Show SMILES CN1CN(C\C=C\C(O)=O)C(=O)N[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C16H19N3O4/c1-18-11-19(9-5-8-14(20)21)16(23)17-13(15(18)22)10-12-6-3-2-4-7-12/h2-8,13H,9-11H2,1H3,(H,17,23)(H,20,21)/b8-5+/t13-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 5 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200324 ((4S,7S)-4,7-dibenzyl-5-methyl-1,3,5-triazepane-2,6...) Show SMILES CN1[C@@H](Cc2ccccc2)NC(=O)N[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C19H21N3O2/c1-22-17(13-15-10-6-3-7-11-15)21-19(24)20-16(18(22)23)12-14-8-4-2-5-9-14/h2-11,16-17H,12-13H2,1H3,(H2,20,21,24)/t16-,17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 10 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair