Compile Data Set for Download or QSAR

Found 10 hits with Last Name = 'franjesevic' and Initial = 'a'   

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
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254293 (CHEMBL4070283) Show SMILES Cl.COc1cc(CN(C)C)ccc1O Show InChI InChI=1S/C10H15NO2/c1-11(2)7-8-4-5-9(12)10(6-8)13-3/h4-6,12H,7H2,1-3H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MMDB PC cid PC sid UniChem Similars	Article PubMed	8.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Mixed type inhibition of Electric eel AChE assessed as inhibition constant using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254289 (CHEMBL4091215) Show SMILES Cl.COc1cc(CN2CCCC2)ccc1O Show InChI InChI=1S/C12H17NO2/c1-15-12-8-10(4-5-11(12)14)9-13-6-2-3-7-13/h4-5,8,14H,2-3,6-7,9H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	9.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Mixed type inhibition of Electric eel AChE assessed as inhibition constant using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254288 (CHEMBL4074057) Show SMILES Cl.COc1cc(CN2CCCCC2)ccc1O Show InChI InChI=1S/C13H19NO2/c1-16-13-9-11(5-6-12(13)15)10-14-7-3-2-4-8-14/h5-6,9,15H,2-4,7-8,10H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	1.06E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Mixed type inhibition of Electric eel AChE assessed as inhibition constant using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254287 (CHEMBL4094588) Show SMILES Cl.COc1cc(CN2CCOCC2)ccc1O Show InChI InChI=1S/C12H17NO3/c1-15-12-8-10(2-3-11(12)14)9-13-4-6-16-7-5-13/h2-3,8,14H,4-7,9H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	1.57E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Mixed type inhibition of Electric eel AChE assessed as inhibition constant using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254288 (CHEMBL4074057) Show SMILES Cl.COc1cc(CN2CCCCC2)ccc1O Show InChI InChI=1S/C13H19NO2/c1-16-13-9-11(5-6-12(13)15)10-14-7-3-2-4-8-14/h5-6,9,15H,2-4,7-8,10H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.27E+5	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Inhibition of Electric eel AChE using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254289 (CHEMBL4091215) Show SMILES Cl.COc1cc(CN2CCCC2)ccc1O Show InChI InChI=1S/C12H17NO2/c1-15-12-8-10(4-5-11(12)14)9-13-6-2-3-7-13/h4-5,8,14H,2-3,6-7,9H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	4.03E+5	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Inhibition of Electric eel AChE using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254293 (CHEMBL4070283) Show SMILES Cl.COc1cc(CN(C)C)ccc1O Show InChI InChI=1S/C10H15NO2/c1-11(2)7-8-4-5-9(12)10(6-8)13-3/h4-6,12H,7H2,1-3H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.19E+5	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Inhibition of Electric eel AChE using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50254287 (CHEMBL4094588) Show SMILES Cl.COc1cc(CN2CCOCC2)ccc1O Show InChI InChI=1S/C12H17NO3/c1-15-12-8-10(2-3-11(12)14)9-13-4-6-16-7-5-13/h2-3,8,14H,4-7,9H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.83E+6	n/a	n/a	n/a	n/a	n/a	n/a
Department of Chemistry and Biochemistry, The Ohio State University, Marion Campus, 1465 Mt. Vernon Avenue, Marion, Ohio 43302, United States. Curated by ChEMBL					Assay Description Inhibition of Electric eel AChE using acetylthiocholine as substrate after 7 min by Ellman's method				ACS Med Chem Lett 8: 622-627 (2017) Article DOI: 10.1021/acsmedchemlett.7b00037 BindingDB Entry DOI: 10.7270/Q20V8G76
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50465496 (CHEMBL4287206) Show SMILES Oc1cccnc1CN1CCCC1 Show InChI InChI=1S/C10H14N2O/c13-10-4-3-5-11-9(10)8-12-6-1-2-7-12/h3-5,13H,1-2,6-8H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	1.02E+6	n/a	n/a	n/a	n/a
The Ohio State University-Marion Curated by ChEMBL					Assay Description Resurrection of isopropyl phosphate-aged electric eel AChE assessed as enzyme reactivation using acetylthiocholine as substrate at pH 9 after 1 day b...				J Med Chem 61: 7034-7042 (2018) Article DOI: 10.1021/acs.jmedchem.7b01620 BindingDB Entry DOI: 10.7270/Q23B62TV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50465496 (CHEMBL4287206) Show SMILES Oc1cccnc1CN1CCCC1 Show InChI InChI=1S/C10H14N2O/c13-10-4-3-5-11-9(10)8-12-6-1-2-7-12/h3-5,13H,1-2,6-8H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	1.21E+6	n/a	n/a	n/a	n/a
The Ohio State University-Marion Curated by ChEMBL					Assay Description Resurrection of methylphosphonate-aged electric eel AChE assessed as enzyme reactivation using acetylthiocholine as substrate at pH 9 after 1 day by ...				J Med Chem 61: 7034-7042 (2018) Article DOI: 10.1021/acs.jmedchem.7b01620 BindingDB Entry DOI: 10.7270/Q23B62TV
					More data for this Ligand-Target Pair