Compile Data Set for Download or QSAR

Found 13 hits with Last Name = 'rostom' and Initial = 'aa'   

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
Neutrophil elastase (Homo sapiens (Human))	BDBM50089098 (CHEMBL266704 | Cys-Phe-Leu-Glu-Ala-Ile-Pro-Met-Asp...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@H]1C(=O)N[C@H](CCC(O)=O)C(O)=O Show InChI InChI=1S/C68H107N13O19S2/c1-10-38(5)54(77-56(87)40(7)70-58(89)43(23-25-52(83)84)71-60(91)46(34-37(3)4)75-61(92)47(35-41-18-13-12-14-19-41)74-57(88)42(69)27-32-101-8)66(97)80-30-16-21-50(80)63(94)72-44(28-33-102-9)59(90)76-48(36-82)62(93)78-55(39(6)11-2)67(98)81-31-17-22-51(81)65(96)79-29-15-20-49(79)64(95)73-45(68(99)100)24-26-53(85)86/h12-14,18-19,37-40,42-51,54-55,82H,10-11,15-17,20-36,69H2,1-9H3,(H,70,89)(H,71,91)(H,72,94)(H,73,95)(H,74,88)(H,75,92)(H,76,90)(H,77,87)(H,78,93)(H,83,84)(H,85,86)(H,99,100)/t38-,39-,40-,42-,43-,44+,45-,46-,47-,48+,49+,50+,51-,54-,55+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Human neutrophil elastase using the reporter substrate MeO-AAPV-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Neutrophil elastase (Homo sapiens (Human))	BDBM50089095 (CHEMBL216418 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser...) Show SMILES CC[C@@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@@H]1CCCN1C(=O)[C@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)[C@H](C)CC)C(O)=O Show InChI InChI=1S/C53H86N10O14S2/c1-10-30(5)42(52(75)63-23-15-18-40(63)51(74)57-36(22-25-79-9)47(70)60-39(28-64)50(73)62-43(53(76)77)31(6)11-2)61-44(67)32(7)55-46(69)35(19-20-41(65)66)56-48(71)37(26-29(3)4)59-49(72)38(27-33-16-13-12-14-17-33)58-45(68)34(54)21-24-78-8/h12-14,16-17,29-32,34-40,42-43,64H,10-11,15,18-28,54H2,1-9H3,(H,55,69)(H,56,71)(H,57,74)(H,58,68)(H,59,72)(H,60,70)(H,61,67)(H,62,73)(H,65,66)(H,76,77)/t30-,31-,32-,34-,35-,36+,37-,38-,39+,40+,42-,43+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Human neutrophil elastase using the reporter substrate MeO-AAPV-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsin-like elastase family member 2A (Sus scrofa)	BDBM50089095 (CHEMBL216418 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser...) Show SMILES CC[C@@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@@H]1CCCN1C(=O)[C@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)[C@H](C)CC)C(O)=O Show InChI InChI=1S/C53H86N10O14S2/c1-10-30(5)42(52(75)63-23-15-18-40(63)51(74)57-36(22-25-79-9)47(70)60-39(28-64)50(73)62-43(53(76)77)31(6)11-2)61-44(67)32(7)55-46(69)35(19-20-41(65)66)56-48(71)37(26-29(3)4)59-49(72)38(27-33-16-13-12-14-17-33)58-45(68)34(54)21-24-78-8/h12-14,16-17,29-32,34-40,42-43,64H,10-11,15,18-28,54H2,1-9H3,(H,55,69)(H,56,71)(H,57,74)(H,58,68)(H,59,72)(H,60,70)(H,61,67)(H,62,73)(H,65,66)(H,76,77)/t30-,31-,32-,34-,35-,36+,37-,38-,39+,40+,42-,43+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Peptide was tested for inhibition constant for competitive inhibition using Suc-AAPA-pNa and Pancreatic elastase				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsinogen A (Bos taurus (bovine))	BDBM50089095 (CHEMBL216418 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser...) Show SMILES CC[C@@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@@H]1CCCN1C(=O)[C@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)[C@H](C)CC)C(O)=O Show InChI InChI=1S/C53H86N10O14S2/c1-10-30(5)42(52(75)63-23-15-18-40(63)51(74)57-36(22-25-79-9)47(70)60-39(28-64)50(73)62-43(53(76)77)31(6)11-2)61-44(67)32(7)55-46(69)35(19-20-41(65)66)56-48(71)37(26-29(3)4)59-49(72)38(27-33-16-13-12-14-17-33)58-45(68)34(54)21-24-78-8/h12-14,16-17,29-32,34-40,42-43,64H,10-11,15,18-28,54H2,1-9H3,(H,55,69)(H,56,71)(H,57,74)(H,58,68)(H,59,72)(H,60,70)(H,61,67)(H,62,73)(H,65,66)(H,76,77)/t30-,31-,32-,34-,35-,36+,37-,38-,39+,40+,42-,43+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Chymotrypsinogen using the reporter substrate Suc-AAPA-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsin-like elastase family member 2A (Sus scrofa)	BDBM50089098 (CHEMBL266704 | Cys-Phe-Leu-Glu-Ala-Ile-Pro-Met-Asp...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@H]1C(=O)N[C@H](CCC(O)=O)C(O)=O Show InChI InChI=1S/C68H107N13O19S2/c1-10-38(5)54(77-56(87)40(7)70-58(89)43(23-25-52(83)84)71-60(91)46(34-37(3)4)75-61(92)47(35-41-18-13-12-14-19-41)74-57(88)42(69)27-32-101-8)66(97)80-30-16-21-50(80)63(94)72-44(28-33-102-9)59(90)76-48(36-82)62(93)78-55(39(6)11-2)67(98)81-31-17-22-51(81)65(96)79-29-15-20-49(79)64(95)73-45(68(99)100)24-26-53(85)86/h12-14,18-19,37-40,42-51,54-55,82H,10-11,15-17,20-36,69H2,1-9H3,(H,70,89)(H,71,91)(H,72,94)(H,73,95)(H,74,88)(H,75,92)(H,76,90)(H,77,87)(H,78,93)(H,83,84)(H,85,86)(H,99,100)/t38-,39-,40-,42-,43-,44+,45-,46-,47-,48+,49+,50+,51-,54-,55+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Peptide was tested for inhibition constant for competitive inhibition using Suc-AAPA-pNa and Pancreatic elastase				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Neutrophil elastase (Homo sapiens (Human))	BDBM50089094 (CHEMBL414810 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C47H75N9O13S2/c1-8-27(4)38(46(67)56-20-12-15-36(56)45(66)51-32(19-22-71-7)42(63)54-35(25-57)47(68)69)55-39(60)28(5)49-41(62)31(16-17-37(58)59)50-43(64)33(23-26(2)3)53-44(65)34(24-29-13-10-9-11-14-29)52-40(61)30(48)18-21-70-6/h9-11,13-14,26-28,30-36,38,57H,8,12,15-25,48H2,1-7H3,(H,49,62)(H,50,64)(H,51,66)(H,52,61)(H,53,65)(H,54,63)(H,55,60)(H,58,59)(H,68,69)/t27-,28-,30-,31-,32+,33-,34-,35+,36+,38-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Human neutrophil elastase using the reporter substrate MeO-AAPV-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsinogen A (Bos taurus (bovine))	BDBM50089098 (CHEMBL266704 | Cys-Phe-Leu-Glu-Ala-Ile-Pro-Met-Asp...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@H]1C(=O)N[C@H](CCC(O)=O)C(O)=O Show InChI InChI=1S/C68H107N13O19S2/c1-10-38(5)54(77-56(87)40(7)70-58(89)43(23-25-52(83)84)71-60(91)46(34-37(3)4)75-61(92)47(35-41-18-13-12-14-19-41)74-57(88)42(69)27-32-101-8)66(97)80-30-16-21-50(80)63(94)72-44(28-33-102-9)59(90)76-48(36-82)62(93)78-55(39(6)11-2)67(98)81-31-17-22-51(81)65(96)79-29-15-20-49(79)64(95)73-45(68(99)100)24-26-53(85)86/h12-14,18-19,37-40,42-51,54-55,82H,10-11,15-17,20-36,69H2,1-9H3,(H,70,89)(H,71,91)(H,72,94)(H,73,95)(H,74,88)(H,75,92)(H,76,90)(H,77,87)(H,78,93)(H,83,84)(H,85,86)(H,99,100)/t38-,39-,40-,42-,43-,44+,45-,46-,47-,48+,49+,50+,51-,54-,55+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Chymotrypsinogen using the reporter substrate Suc-AAPA-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Neutrophil elastase (Homo sapiens (Human))	BDBM50089096 (CHEMBL278549 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met | e...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(O)=O Show InChI InChI=1S/C44H70N8O11S2/c1-8-26(4)36(43(61)52-20-12-15-34(52)42(60)48-31(44(62)63)19-22-65-7)51-37(55)27(5)46-39(57)30(16-17-35(53)54)47-40(58)32(23-25(2)3)50-41(59)33(24-28-13-10-9-11-14-28)49-38(56)29(45)18-21-64-6/h9-11,13-14,25-27,29-34,36H,8,12,15-24,45H2,1-7H3,(H,46,57)(H,47,58)(H,48,60)(H,49,56)(H,50,59)(H,51,55)(H,53,54)(H,62,63)/t26-,27-,29-,30-,31+,32-,33-,34+,36-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Human neutrophil elastase using the reporter substrate MeO-AAPV-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50089097 (CHEMBL21028 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Lys) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@H](CCCCN)C(O)=O Show InChI InChI=1S/C45H73N9O11S/c1-7-27(4)37(44(63)54-22-13-17-35(54)43(62)50-32(45(64)65)16-11-12-21-46)53-38(57)28(5)48-40(59)31(18-19-36(55)56)49-41(60)33(24-26(2)3)52-42(61)34(25-29-14-9-8-10-15-29)51-39(58)30(47)20-23-66-6/h8-10,14-15,26-28,30-35,37H,7,11-13,16-25,46-47H2,1-6H3,(H,48,59)(H,49,60)(H,50,62)(H,51,58)(H,52,61)(H,53,57)(H,55,56)(H,64,65)/t27-,28-,30-,31-,32-,33-,34-,35+,37-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against trypsin using the reporter substrate Ac-R-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsin-like elastase family member 2A (Sus scrofa)	BDBM50089099 ((S)-2-{(S)-2-[(S)-2-((S)-2-Amino-4-methylsulfanyl-...) Show SMILES CSCC[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O Show InChI InChI=1S/C23H36N4O5S/c1-14(2)12-18(21(29)25-15(3)23(31)32)27-22(30)19(13-16-8-6-5-7-9-16)26-20(28)17(24)10-11-33-4/h5-9,14-15,17-19H,10-13,24H2,1-4H3,(H,25,29)(H,26,28)(H,27,30)(H,31,32)/t15-,17-,18-,19-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.10E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Peptide was tested for inhibition constant for competitive inhibition using Suc-AAPA-pNa and Pancreatic elastase				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsinogen A (Bos taurus (bovine))	BDBM50089096 (CHEMBL278549 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met | e...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(O)=O Show InChI InChI=1S/C44H70N8O11S2/c1-8-26(4)36(43(61)52-20-12-15-34(52)42(60)48-31(44(62)63)19-22-65-7)51-37(55)27(5)46-39(57)30(16-17-35(53)54)47-40(58)32(23-25(2)3)50-41(59)33(24-28-13-10-9-11-14-28)49-38(56)29(45)18-21-64-6/h9-11,13-14,25-27,29-34,36H,8,12,15-24,45H2,1-7H3,(H,46,57)(H,47,58)(H,48,60)(H,49,56)(H,50,59)(H,51,55)(H,53,54)(H,62,63)/t26-,27-,29-,30-,31+,32-,33-,34+,36-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Chymotrypsinogen using the reporter substrate Suc-AAPA-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsinogen A (Bos taurus (bovine))	BDBM50089094 (CHEMBL414810 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C47H75N9O13S2/c1-8-27(4)38(46(67)56-20-12-15-36(56)45(66)51-32(19-22-71-7)42(63)54-35(25-57)47(68)69)55-39(60)28(5)49-41(62)31(16-17-37(58)59)50-43(64)33(23-26(2)3)53-44(65)34(24-29-13-10-9-11-14-29)52-40(61)30(48)18-21-70-6/h9-11,13-14,26-28,30-36,38,57H,8,12,15-25,48H2,1-7H3,(H,49,62)(H,50,64)(H,51,66)(H,52,61)(H,53,65)(H,54,63)(H,55,60)(H,58,59)(H,68,69)/t27-,28-,30-,31-,32+,33-,34-,35+,36+,38-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.10E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Competitive inhibition constant of the compound was tested against Chymotrypsinogen using the reporter substrate Suc-AAPA-pNa				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair
Chymotrypsin-like elastase family member 2A (Sus scrofa)	BDBM50089094 (CHEMBL414810 | Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C47H75N9O13S2/c1-8-27(4)38(46(67)56-20-12-15-36(56)45(66)51-32(19-22-71-7)42(63)54-35(25-57)47(68)69)55-39(60)28(5)49-41(62)31(16-17-37(58)59)50-43(64)33(23-26(2)3)53-44(65)34(24-29-13-10-9-11-14-29)52-40(61)30(48)18-21-70-6/h9-11,13-14,26-28,30-36,38,57H,8,12,15-25,48H2,1-7H3,(H,49,62)(H,50,64)(H,51,66)(H,52,61)(H,53,65)(H,54,63)(H,55,60)(H,58,59)(H,68,69)/t27-,28-,30-,31-,32+,33-,34-,35+,36+,38-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.80E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Oxford Centre for Molecular Sciences Curated by ChEMBL					Assay Description Peptide was tested for inhibition constant for competitive inhibition using Suc-AAPA-pNa and Pancreatic elastase				Bioorg Med Chem Lett 10: 1219-21 (2000) BindingDB Entry DOI: 10.7270/Q2FQ9VTD
					More data for this Ligand-Target Pair