Compile Data Set for Download or QSAR

Found 4 hits with Last Name = 'payrot' and Initial = 'n'   

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
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50484283 (CHEMBL1830070) Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ncnc2n(-[#6]-[#6]-[#8]-[#6]P([#16-])(=O)[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)cnc12 Show InChI InChI=1S/C8H14N5O9P3S.4Na/c9-7-6-8(11-3-10-7)13(4-12-6)1-2-20-5-23(14,26)21-25(18,19)22-24(15,16)17;;;;/h3-4H,1-2,5H2,(H,14,26)(H,18,19)(H2,9,10,11)(H2,15,16,17);;;;/q;4*+1/p-4	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£s Aix-Marseille I et II Curated by ChEMBL					Assay Description Inhibition of wild-type HIV1 subtype B reverse transcriptase assessed as incorporation of [3H]dTTP				Eur J Med Chem 46: 4281-8 (2011) Article DOI: 10.1016/j.ejmech.2011.06.034 BindingDB Entry DOI: 10.7270/Q2MW2M0C
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50484282 (CHEMBL1830071) Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ncnc2n(-[#6]-[#6]-[#8]-[#6]P([#8-])(=O)[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)cnc12 Show InChI InChI=1S/C8H14N5O10P3/c9-7-6-8(11-3-10-7)13(4-12-6)1-2-21-5-24(14,15)22-26(19,20)23-25(16,17)18/h3-4H,1-2,5H2,(H,14,15)(H,19,20)(H2,9,10,11)(H2,16,17,18)/p-4	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£s Aix-Marseille I et II Curated by ChEMBL					Assay Description Inhibition of wild-type HIV1 subtype B reverse transcriptase assessed as incorporation of [3H]dTTP				Eur J Med Chem 46: 4281-8 (2011) Article DOI: 10.1016/j.ejmech.2011.06.034 BindingDB Entry DOI: 10.7270/Q2MW2M0C
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50484281 (CHEMBL1830073) Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[#6]-[#6@H](-[#6]-n1cnc2c(-[#7])ncnc12)-[#8]-[#6]P([#8-])(=O)[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O |r| Show InChI InChI=1S/C9H16N5O10P3.4Na/c1-6(2-14-4-13-7-8(10)11-3-12-9(7)14)22-5-25(15,16)23-27(20,21)24-26(17,18)19;;;;/h3-4,6H,2,5H2,1H3,(H,15,16)(H,20,21)(H2,10,11,12)(H2,17,18,19);;;;/q;4*+1/p-4/t6-;;;;/m1..../s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.13E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£s Aix-Marseille I et II Curated by ChEMBL					Assay Description Inhibition of wild-type HIV1 subtype B reverse transcriptase assessed as incorporation of [3H]dTTP				Eur J Med Chem 46: 4281-8 (2011) Article DOI: 10.1016/j.ejmech.2011.06.034 BindingDB Entry DOI: 10.7270/Q2MW2M0C
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50484284 (CHEMBL1830072) Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[#6]-[#6@H](-[#6]-n1cnc2c(-[#7])ncnc12)-[#8]-[#6]P([#16-])(=O)[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O |r| Show InChI InChI=1S/C9H16N5O9P3S.4Na/c1-6(2-14-4-13-7-8(10)11-3-12-9(7)14)21-5-24(15,27)22-26(19,20)23-25(16,17)18;;;;/h3-4,6H,2,5H2,1H3,(H,15,27)(H,19,20)(H2,10,11,12)(H2,16,17,18);;;;/q;4*+1/p-4/t6-,24?;;;;/m1..../s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£s Aix-Marseille I et II Curated by ChEMBL					Assay Description Inhibition of wild-type HIV1 subtype B reverse transcriptase assessed as incorporation of [3H]dTTP				Eur J Med Chem 46: 4281-8 (2011) Article DOI: 10.1016/j.ejmech.2011.06.034 BindingDB Entry DOI: 10.7270/Q2MW2M0C
					More data for this Ligand-Target Pair