Compile Data Set for Download or QSAR

Found 32 hits with Last Name = 'boyd' and Initial = 'mr'   

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
Protein kinase C zeta type (Rattus norvegicus)	BDBM50478518 (CHEMBL514017) Show SMILES [H][C@]12[C@]3([H])C=C(CO)C[C@]4(O)C(=O)C(C)=C[C@@]4([H])[C@@]3(O)[C@@H](C)C[C@@]1(OC(=O)C\C=C\C=C\CCCC)C2(C)C |r,c:14,t:4| Show InChI InChI=1S/C30H42O6/c1-6-7-8-9-10-11-12-13-24(32)36-29-16-20(3)30(35)22(25(29)27(29,4)5)15-21(18-31)17-28(34)23(30)14-19(2)26(28)33/h9-12,14-15,20,22-23,25,31,34-35H,6-8,13,16-18H2,1-5H3/b10-9+,12-11+/t20-,22-,23+,25+,28+,29-,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Displacement of [3H]PDBu from rat brain membrane PKC				J Nat Prod 58: 769-72 (1995) Article DOI: 10.1021/np50119a020 BindingDB Entry DOI: 10.7270/Q2NZ8BF5
					More data for this Ligand-Target Pair
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50090045 ((2,3-Dihydroxy-4-methoxy-phenyl)-(3,4,5-trimethoxy...) Show SMILES COc1ccc(C(=O)c2cc(OC)c(OC)c(OC)c2)c(O)c1O Show InChI InChI=1S/C17H18O7/c1-21-11-6-5-10(15(19)16(11)20)14(18)9-7-12(22-2)17(24-4)13(8-9)23-3/h5-8,19-20H,1-4H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	820	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description Inhibition of tubulin polymerization				J Med Chem 43: 2731-7 (2000) BindingDB Entry DOI: 10.7270/Q2SX6CFQ
					More data for this Ligand-Target Pair
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50005480 ((-)-combretastatin | (Z)-3'-hydroxy-3,4,4',5-tetra...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)cc1O Show InChI InChI=1S/C18H20O5/c1-20-15-8-7-12(9-14(15)19)5-6-13-10-16(21-2)18(23-4)17(11-13)22-3/h5-11,19H,1-4H3/b6-5-	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description Inhibition of tubulin polymerization				J Med Chem 43: 2731-7 (2000) BindingDB Entry DOI: 10.7270/Q2SX6CFQ
					More data for this Ligand-Target Pair				3D Structure (crystal)
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50090044 ((Z)-2',3'-dihydroxy-3,4,4',5-tetramethoxystilbene ...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)c(O)c1O Show InChI InChI=1S/C18H20O6/c1-21-13-8-7-12(16(19)17(13)20)6-5-11-9-14(22-2)18(24-4)15(10-11)23-3/h5-10,19-20H,1-4H3/b6-5-	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description Inhibition of tubulin polymerization				J Med Chem 43: 2731-7 (2000) BindingDB Entry DOI: 10.7270/Q2SX6CFQ
					More data for this Ligand-Target Pair
Similar to alpha-tubulin isoform 1 (Bos taurus)	BDBM50005480 ((-)-combretastatin | (Z)-3'-hydroxy-3,4,4',5-tetra...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)cc1O Show InChI InChI=1S/C18H20O5/c1-20-15-8-7-12(9-14(15)19)5-6-13-10-16(21-2)18(23-4)17(11-13)22-3/h5-11,19H,1-4H3/b6-5-	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description The compound was tested for the concentration to inhibit 50% of tubulin polymerization.				J Med Chem 41: 1688-95 (1998) Article DOI: 10.1021/jm970644q BindingDB Entry DOI: 10.7270/Q2N300QZ
					More data for this Ligand-Target Pair
Similar to alpha-tubulin isoform 1 (Bos taurus)	BDBM50006677 (1,2,3-Trimethoxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)cc1 Show InChI InChI=1S/C18H20O4/c1-19-15-9-7-13(8-10-15)5-6-14-11-16(20-2)18(22-4)17(12-14)21-3/h5-12H,1-4H3/b6-5-	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description The compound was tested for the concentration to inhibit 50% of tubulin polymerization.				J Med Chem 41: 1688-95 (1998) Article DOI: 10.1021/jm970644q BindingDB Entry DOI: 10.7270/Q2N300QZ
					More data for this Ligand-Target Pair
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50014846 ((S)-N-(5,6,7,9-tetrahydro-1,2,3,10-tetramethoxy-9-...) Show SMILES COc1cc2CC[C@H](NC(C)=O)c3cc(=O)c(OC)ccc3-c2c(OC)c1OC |r| Show InChI InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)/t16-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	MMDB PDB Article	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50 % inhibition of tubulin polymerization by turbidimetric assay				Bioorg Med Chem Lett 3: 581-584 (1993) Article DOI: 10.1016/S0960-894X(01)81233-6 BindingDB Entry DOI: 10.7270/Q29G5N91
					More data for this Ligand-Target Pair				3D Structure (crystal)
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50064891 (5,7,3'-trihydroxy-3,6-4'-trimethoxyflavone | 5,7-D...) Show SMILES COc1ccc(cc1O)-c1oc2cc(O)c(OC)c(O)c2c(=O)c1OC Show InChI InChI=1S/C18H16O8/c1-23-11-5-4-8(6-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50 % inhibition of tubulin polymerization by turbidimetric assay				Bioorg Med Chem Lett 3: 581-584 (1993) Article DOI: 10.1016/S0960-894X(01)81233-6 BindingDB Entry DOI: 10.7270/Q29G5N91
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478521 (CHEMBL465805) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)[C@H](O)[C@@H](O)CC2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C30H48O4/c1-25(2)14-15-30(24(33)34)13-10-20-27(5)11-8-19-26(3,4)16-18(31)23(32)29(19,7)21(27)9-12-28(20,6)22(30)17-25/h10,18-19,21-23,31-32H,8-9,11-17H2,1-7H3,(H,33,34)/t18-,19-,21-,22+,23+,27-,28+,29-,30+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Similar to alpha-tubulin isoform 1 (Bos taurus)	BDBM50471653 (CHEMBL297299) Show SMILES COc1ccc(cc1OC(C)=O)C(=O)c1cc(OC)c(OC)c(OC)c1 Show InChI InChI=1S/C19H20O7/c1-11(20)26-15-8-12(6-7-14(15)22-2)18(21)13-9-16(23-3)19(25-5)17(10-13)24-4/h6-10H,1-5H3	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description The compound was tested for the concentration to inhibit 50% of tubulin polymerization.				J Med Chem 41: 1688-95 (1998) Article DOI: 10.1021/jm970644q BindingDB Entry DOI: 10.7270/Q2N300QZ
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50292441 (1beta-hydroxyaleuritolic acid 3-p-hydroxybenzoate ...) Show SMILES CC1(C)CC[C@@]2(CC=C3[C@]4(C)CC[C@H]5C(C)(C)[C@H](C[C@@H](O)[C@]5(C)[C@H]4CC[C@@]3(C)[C@H]2C1)OC(=O)c1ccc(O)cc1)C(O)=O |r,t:7| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-25-34(5)15-12-24-33(3,4)29(43-30(40)22-8-10-23(38)11-9-22)20-28(39)36(24,7)26(34)13-16-35(25,6)27(37)21-32/h8-11,14,24,26-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,26-,27+,28+,29-,34-,35+,36-,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478525 (CHEMBL465804) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)[C@H](O)C[C@H](O)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C30H48O4/c1-25(2)14-15-30(24(33)34)13-10-19-27(5)11-8-18-26(3,4)22(31)16-23(32)29(18,7)20(27)9-12-28(19,6)21(30)17-25/h10,18,20-23,31-32H,8-9,11-17H2,1-7H3,(H,33,34)/t18-,20-,21+,22-,23+,27-,28+,29-,30+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478526 (CHEMBL448121) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](OC(=O)c1ccc(O)cc1)[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C44H56O8/c1-39(2)22-23-44(38(49)50)21-18-32-41(5)19-16-31-40(3,4)35(52-37(48)27-10-14-29(46)15-11-27)30(51-36(47)26-8-12-28(45)13-9-26)24-43(31,7)33(41)17-20-42(32,6)34(44)25-39/h8-15,18,30-31,33-35,45-46H,16-17,19-25H2,1-7H3,(H,49,50)/t30-,31+,33+,34-,35+,41+,42-,43+,44-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478416 (CHEBI:65536 | CHEMBL444821) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#8]-c1c(-[#6]\[#6]=[#6](\[#6])-[#6])c(-[#8])nc2ccccc12 Show InChI InChI=1S/C19H23NO2/c1-13(2)9-10-16-18(22-12-11-14(3)4)15-7-5-6-8-17(15)20-19(16)21/h5-9,11H,10,12H2,1-4H3,(H,20,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 reverse transcriptase				J Nat Prod 59: 469-71 (1996) Article DOI: 10.1021/np960250m BindingDB Entry DOI: 10.7270/Q2XK8J9J
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478527 (Aleuritolic Acid 3-P-Hydroxybenzoate | CHEMBL45689...) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O5/c1-32(2)20-21-37(31(40)41)19-14-27-35(6)16-12-25-33(3,4)29(42-30(39)23-8-10-24(38)11-9-23)15-18-34(25,5)26(35)13-17-36(27,7)28(37)22-32/h8-11,14,25-26,28-29,38H,12-13,15-22H2,1-7H3,(H,40,41)/t25-,26+,28+,29-,34-,35+,36+,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.06E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478523 (Aleuritolic Acid 3-P-Hydroxycinnamate | CHEMBL5033...) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](OC(=O)\C=C\c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C39H54O5/c1-34(2)22-23-39(33(42)43)21-16-29-37(6)18-14-27-35(3,4)31(44-32(41)13-10-25-8-11-26(40)12-9-25)17-20-36(27,5)28(37)15-19-38(29,7)30(39)24-34/h8-13,16,27-28,30-31,40H,14-15,17-24H2,1-7H3,(H,42,43)/b13-10+/t27-,28+,30+,31-,36-,37+,38+,39+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478415 (Buchapine | CHEBI:65535) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]C1([#6](=O)-[#7]-c2ccccc2-[#6]1=O)C([#6])([#6])[#6]=[#6] Show InChI InChI=1S/C19H23NO2/c1-6-18(4,5)19(12-11-13(2)3)16(21)14-9-7-8-10-15(14)20-17(19)22/h6-11H,1,12H2,2-5H3,(H,20,22)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	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
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 reverse transcriptase				J Nat Prod 59: 469-71 (1996) Article DOI: 10.1021/np960250m BindingDB Entry DOI: 10.7270/Q2XK8J9J
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478524 (CHEMBL450856) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](O)[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(43-30(40)22-8-10-23(38)11-9-22)24(39)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25+,27+,28-,29+,34+,35-,36+,37-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478522 (CHEMBL454238) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@H](OC(=O)c1ccc(O)cc1)[C@@H](O)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(39)24(43-30(40)22-8-10-23(38)11-9-22)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25-,27-,28+,29+,34-,35+,36-,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Similar to alpha-tubulin isoform 1 (Bos taurus)	BDBM50471654 (CHEMBL44574) Show SMILES [Na;v0+].[#6]-[#8]-c1ccc(cc1-[#8]P([#8])([#8-])=O)-[#6](=O)-c1cc(-[#8]-[#6])c(-[#8]-[#6])c(-[#8]-[#6])c1 Show InChI InChI=1S/C17H19O9P/c1-22-12-6-5-10(7-13(12)26-27(19,20)21)16(18)11-8-14(23-2)17(25-4)15(9-11)24-3/h5-9H,1-4H3,(H2,19,20,21)/p-1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description The compound was tested for the concentration to inhibit 50% of tubulin polymerization.				J Med Chem 41: 1688-95 (1998) Article DOI: 10.1021/jm970644q BindingDB Entry DOI: 10.7270/Q2N300QZ
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478522 (CHEMBL454238) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@H](OC(=O)c1ccc(O)cc1)[C@@H](O)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(39)24(43-30(40)22-8-10-23(38)11-9-22)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25-,27-,28+,29+,34-,35+,36-,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50090046 (CHEMBL329267 | Phosphoric acid mono-[3-methoxy-2-p...) Show SMILES COc1ccc(C(=O)c2cc(OC)c(OC)c(OC)c2)c(OP([O-])([O-])=O)c1OP([O-])([O-])=O Show InChI InChI=1S/C17H20O13P2/c1-25-11-6-5-10(15(29-31(19,20)21)17(11)30-32(22,23)24)14(18)9-7-12(26-2)16(28-4)13(8-9)27-3/h5-8H,1-4H3,(H2,19,20,21)(H2,22,23,24)/p-4	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description Inhibition of tubulin polymerization				J Med Chem 43: 2731-7 (2000) BindingDB Entry DOI: 10.7270/Q2SX6CFQ
					More data for this Ligand-Target Pair
Tubulin alpha-1A chain (Sus scrofa (Pig))	BDBM50064259 (CHEMBL289351 | Combretastatin A4 phosphate | Di-So...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)cc1OP([O-])([O-])=O Show InChI InChI=1S/C18H21O8P/c1-22-14-8-7-12(9-15(14)26-27(19,20)21)5-6-13-10-16(23-2)18(25-4)17(11-13)24-3/h5-11H,1-4H3,(H2,19,20,21)/p-2/b6-5-	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description Inhibition of tubulin polymerization				J Med Chem 43: 2731-7 (2000) BindingDB Entry DOI: 10.7270/Q2SX6CFQ
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478528 (CHEMBL451536) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](OC(=O)c1ccc(O)cc1)[C@H](O)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(39)24(43-30(40)22-8-10-23(38)11-9-22)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25+,27+,28-,29+,34+,35-,36+,37-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by UIC assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478526 (CHEMBL448121) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](OC(=O)c1ccc(O)cc1)[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C44H56O8/c1-39(2)22-23-44(38(49)50)21-18-32-41(5)19-16-31-40(3,4)35(52-37(48)27-10-14-29(46)15-11-27)30(51-36(47)26-8-12-28(45)13-9-26)24-43(31,7)33(41)17-20-42(32,6)34(44)25-39/h8-15,18,30-31,33-35,45-46H,16-17,19-25H2,1-7H3,(H,49,50)/t30-,31+,33+,34-,35+,41+,42-,43+,44-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478523 (Aleuritolic Acid 3-P-Hydroxycinnamate | CHEMBL5033...) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](OC(=O)\C=C\c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C39H54O5/c1-34(2)22-23-39(33(42)43)21-16-29-37(6)18-14-27-35(3,4)31(44-32(41)13-10-25-8-11-26(40)12-9-25)17-20-36(27,5)28(37)15-19-38(29,7)30(39)24-34/h8-13,16,27-28,30-31,40H,14-15,17-24H2,1-7H3,(H,42,43)/b13-10+/t27-,28+,30+,31-,36-,37+,38+,39+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Similar to alpha-tubulin isoform 1 (Bos taurus)	BDBM50064259 (CHEMBL289351 | Combretastatin A4 phosphate | Di-So...) Show SMILES COc1ccc(\C=C/c2cc(OC)c(OC)c(OC)c2)cc1OP([O-])([O-])=O Show InChI InChI=1S/C18H21O8P/c1-22-14-8-7-12(9-15(14)26-27(19,20)21)5-6-13-10-16(23-2)18(25-4)17(11-13)24-3/h5-11H,1-4H3,(H2,19,20,21)/p-2/b6-5-	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>8.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Arizona State University Curated by ChEMBL					Assay Description The compound was tested for the concentration to inhibit 50% of tubulin polymerization.				J Med Chem 41: 1688-95 (1998) Article DOI: 10.1021/jm970644q BindingDB Entry DOI: 10.7270/Q2N300QZ
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478521 (CHEMBL465805) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)[C@H](O)[C@@H](O)CC2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C30H48O4/c1-25(2)14-15-30(24(33)34)13-10-20-27(5)11-8-19-26(3,4)16-18(31)23(32)29(19,7)21(27)9-12-28(20,6)22(30)17-25/h10,18-19,21-23,31-32H,8-9,11-17H2,1-7H3,(H,33,34)/t18-,19-,21-,22+,23+,27-,28+,29-,30+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50292441 (1beta-hydroxyaleuritolic acid 3-p-hydroxybenzoate ...) Show SMILES CC1(C)CC[C@@]2(CC=C3[C@]4(C)CC[C@H]5C(C)(C)[C@H](C[C@@H](O)[C@]5(C)[C@H]4CC[C@@]3(C)[C@H]2C1)OC(=O)c1ccc(O)cc1)C(O)=O |r,t:7| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-25-34(5)15-12-24-33(3,4)29(43-30(40)22-8-10-23(38)11-9-22)20-28(39)36(24,7)26(34)13-16-35(25,6)27(37)21-32/h8-11,14,24,26-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,26-,27+,28+,29-,34-,35+,36-,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478528 (CHEMBL451536) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](OC(=O)c1ccc(O)cc1)[C@H](O)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(39)24(43-30(40)22-8-10-23(38)11-9-22)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25+,27+,28-,29+,34+,35-,36+,37-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478524 (CHEMBL450856) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)C[C@@H](O)[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O6/c1-32(2)18-19-37(31(41)42)17-14-26-34(5)15-12-25-33(3,4)29(43-30(40)22-8-10-23(38)11-9-22)24(39)20-36(25,7)27(34)13-16-35(26,6)28(37)21-32/h8-11,14,24-25,27-29,38-39H,12-13,15-21H2,1-7H3,(H,41,42)/t24-,25+,27+,28-,29+,34+,35-,36+,37-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair
Reverse transcriptase (Human immunodeficiency virus 1)	BDBM50478527 (Aleuritolic Acid 3-P-Hydroxybenzoate | CHEMBL45689...) Show SMILES [H][C@@]12CC[C@@]3(C)C4=CC[C@]5(CCC(C)(C)C[C@]5([H])[C@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](OC(=O)c1ccc(O)cc1)C2(C)C)C(O)=O |r,t:6| Show InChI InChI=1S/C37H52O5/c1-32(2)20-21-37(31(40)41)19-14-27-35(6)16-12-25-33(3,4)29(42-30(39)23-8-10-24(38)11-9-23)15-18-34(25,5)26(35)13-17-36(27,7)28(37)22-32/h8-11,14,25-26,28-29,38H,12-13,15-22H2,1-7H3,(H,40,41)/t25-,26+,28+,29-,34-,35+,36+,37+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
National Cancer Institute Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant reverse transcriptase by NCI assay				J Nat Prod 58: 1039-46 (1995) Article DOI: 10.1021/np50121a008 BindingDB Entry DOI: 10.7270/Q28S4SP1
					More data for this Ligand-Target Pair