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Found 303 with Last Name = 'saxena' and Initial = 's'
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50427257(CHEMBL2325118)
Affinity DataKi:  5.00E+3nMAssay Description:Competitive inhibition of Mycobacterium tuberculosis CysK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50427257(CHEMBL2325118)
Affinity DataKi:  5.00E+3nMAssay Description:Competitive inhibition of Mycobacterium tuberculosis CysK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM14774(3-(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl...)
Affinity DataIC50:  0.200nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439141(CHEMBL2418481)
Affinity DataIC50:  19nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558593(CHEMBL4747406)
Affinity DataIC50:  25nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439146(CHEMBL2418529)
Affinity DataIC50:  26nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558594(CHEMBL4744412)
Affinity DataIC50:  31nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439147(CHEMBL2418524)
Affinity DataIC50:  34nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439140(CHEMBL2418487)
Affinity DataIC50:  37nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558595(CHEMBL4764245)
Affinity DataIC50:  40nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558598(CHEMBL4756900)
Affinity DataIC50:  44nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDNA gyrase subunit B(Mycobacterium smegmatis)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50226181((3R,4S,5R,6R)-5-hydroxy-6-(4-hydroxy-3-(4-hydroxy-...)
Affinity DataIC50:  46nMAssay Description:Inhibition of Mycobacterium smegmatis 155 6His-tagged DNA gyrase B catalytic domain ATPase activity expressed in Escherichia coli BL21 (DE3) pLysS ce...More data for this Ligand-Target Pair
TargetDNA gyrase subunit B(Mycobacterium smegmatis)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50423645(Albamycin | Cathomycin | NOVOBIOCIN)
Affinity DataIC50:  46nMT: 2°CAssay Description:Inhibition of Mycobacterium smegmatis DNA GyrB domain assessed as inhibition of inorganic phosphate release after 100 mins at room temperature by ATP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558600(CHEMBL4744894)
Affinity DataIC50:  48nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558599(CHEMBL4799096)
Affinity DataIC50:  50nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439143(CHEMBL2418504)
Affinity DataIC50:  54nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439142(CHEMBL2418505)
Affinity DataIC50:  56nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439144(CHEMBL2418502)
Affinity DataIC50:  60nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439152(CHEMBL2418568)
Affinity DataIC50:  63nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558596(CHEMBL4791975)
Affinity DataIC50:  64nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439139(CHEMBL2418489)
Affinity DataIC50:  70nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50248919((S)-N-(2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsu...)
Affinity DataIC50:  74nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439150(CHEMBL2418545)
Affinity DataIC50:  95nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439151(CHEMBL2418569)
Affinity DataIC50:  101nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439138(CHEMBL2418558)
Affinity DataIC50:  103nMAssay Description:Inhibition of Mycobacterium tuberculosis CysK1More data for this Ligand-Target Pair
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439149(CHEMBL2418548)
Affinity DataIC50:  110nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Homo sapiens (Human))
Orchid Pharma

Curated by ChEMBL
LigandPNGBDBM50558597(CHEMBL4787884)
Affinity DataIC50:  127nMAssay Description:Inhibition of human PDE4B using [3H]cAMP as substrate incubated for 5 mins followed by substrate addition and measured after 10 mins by scintillation...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439148(CHEMBL2418551)
Affinity DataIC50:  141nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO-acetylserine sulfhydrylase(Mycobacterium tuberculosis)
Karolinska Institutet

Curated by ChEMBL
LigandPNGBDBM50439145(CHEMBL2418514)
Affinity DataIC50:  160nMAssay Description:Inhibition of Mycobacterium tuberculosis N-terminal His-6-tagged recombinant CysK1 expressed in Escherichia coli BL21 (DE3) after 20 mins by spectrop...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA gyrase subunit B(Mycobacterium smegmatis)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM282((3R,4S,5R,6R)-5-hydroxy-6-[(2-hydroxy-3-{[4-hydrox...)
Affinity DataIC50:  180nMAssay Description:Inhibition of Mycobacterium smegmatis GyrB ATPase activity expressed in Escherichia coli BL21 (DE3) pLysS cells after 100 mins by inorganic phosphate...More data for this Ligand-Target Pair
TargetEnoyl-acyl-carrier protein reductase(Plasmodium falciparum)
Csir-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50135169((-)-Catechin gallate | (2S,3R)-2-(3,4-dihydroxyphe...)
Affinity DataIC50:  300nMAssay Description:Inhibition of Plasmodium falciparum FabIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147729(CHEMBL3765483)
Affinity DataIC50:  520nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147691(CHEMBL3764865)
Affinity DataIC50:  530nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147716(CHEMBL3763241)
Affinity DataIC50:  580nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147695(CHEMBL3765314)
Affinity DataIC50:  640nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147715(CHEMBL3764614)
Affinity DataIC50:  670nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147724(CHEMBL3764280)
Affinity DataIC50:  690nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147725(CHEMBL3765736)
Affinity DataIC50:  740nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147732(CHEMBL3764694)
Affinity DataIC50:  840nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA gyrase subunit B(Mycobacterium smegmatis)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50066107(CHEMBL3402951)
Affinity DataIC50:  860nMT: 2°CAssay Description:Inhibition of Mycobacterium smegmatis DNA GyrB domain assessed as inhibition of inorganic phosphate release after 100 mins at room temperature by ATP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA gyrase subunit B(Mycobacterium smegmatis)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50067153(CHEMBL3403274)
Affinity DataIC50:  950nMAssay Description:Inhibition of Mycobacterium smegmatis GyrB ATPase activity expressed in Escherichia coli BL21 (DE3) pLysS cells after 100 mins by inorganic phosphate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEnoyl-acyl-carrier protein reductase(Plasmodium falciparum)
Csir-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM7457(2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of Plasmodium falciparum FabIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147719(CHEMBL3763769)
Affinity DataIC50:  1.02E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147733(CHEMBL3763165)
Affinity DataIC50:  1.02E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147730(CHEMBL3765612)
Affinity DataIC50:  1.03E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147727(CHEMBL3765386)
Affinity DataIC50:  1.06E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147693(CHEMBL3763613)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProbable L-lysine-epsilon aminotransferase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology & Science-Pilani

Curated by ChEMBL
LigandPNGBDBM50450930(CHEMBL4210409)
Affinity DataIC50:  1.15E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis LAT using L-lysine as substrate by spectroscopic methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147712(CHEMBL3764292)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPantothenate synthetase(Mycobacterium tuberculosis (strain ATCC 25618 / H3...)
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50147696(CHEMBL3763438)
Affinity DataIC50:  1.23E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis pantothenate synthetase using pantoic acid as substrate and beta-alanine as reactant assessed as NAD+ format...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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