Compile Data Set for Download or QSAR
Found 299 with Last Name = 'hori' and Initial = 'n'
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370676(CHEMBL607907)copy SMILEScopy InChI
Affinity DataKi:  1.86E+3nMAssay Description:Inhibitory constant against human galactosyltransferase using UDP-GalMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370674(UDP-GALACTOSE)copy SMILEScopy InChI
Affinity DataKi:  4.91E+3nMAssay Description:Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase IMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370675(CHEMBL607908)copy SMILEScopy InChI
Affinity DataKi:  1.17E+4nMAssay Description:Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase IMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370678(CHEMBL611116)copy SMILEScopy InChI
Affinity DataKi:  2.06E+4nMAssay Description:Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase IMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370677(CHEMBL609634)copy SMILEScopy InChI
Affinity DataKi:  2.23E+4nMAssay Description:Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase IMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50173721(CHEMBL196432 | Uridine-5'-diphosphogalactose deriv...)copy SMILEScopy InChI
Affinity DataKi:  7.67E+4nMAssay Description:Inhibitory constant against human Beta-1,4-galactosyltransferase I using UDP-Gal (0-160 uM)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetBeta-1,4-galactosyltransferase 1(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50370679(CHEMBL611112)copy SMILEScopy InChI
Affinity DataKi:  1.49E+5nMAssay Description:Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase IMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8FPXPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264847(CHEMBL4096902)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50256209(CHEMBL4101768)copy SMILEScopy InChI
Affinity DataIC50: 0.190nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063918((2R,3S)-N*4*-Hydroxy-2-isobutyl-N*1*-((S)-1-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063912((R)-N*4*-Hydroxy-N*1*-((S)-methylcarbamoyl-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264846(CHEMBL4066531)copy SMILEScopy InChI
Affinity DataIC50: 0.210nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192809(CHEMBL3941914)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192809(CHEMBL3941914)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50256228(CHEMBL4099293)copy SMILEScopy InChI
Affinity DataIC50: 0.290nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063915((2R,3S)-N*4*-Hydroxy-2-isobutyl-3-methyl-N*1*-[(S)...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Activity against Matrix metalloproteinase-2 (MMP-2).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192811(CHEMBL3971502)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063915((2R,3S)-N*4*-Hydroxy-2-isobutyl-3-methyl-N*1*-[(S)...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Activity against Matrix metalloproteinase-1 (MMP-1).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063915((2R,3S)-N*4*-Hydroxy-2-isobutyl-3-methyl-N*1*-[(S)...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192811(CHEMBL3971502)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264858(CHEMBL4077638)copy SMILEScopy InChI
Affinity DataIC50: 0.310nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192807(CHEMBL3984947)copy SMILEScopy InChI
Affinity DataIC50: 0.360nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264859(CHEMBL4078117)copy SMILEScopy InChI
Affinity DataIC50: 0.390nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192809(CHEMBL3941914)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of hypotonicity-induced activation pretreated for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192809(CHEMBL3941914)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of hypotonicity-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063918((2R,3S)-N*4*-Hydroxy-2-isobutyl-N*1*-((S)-1-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Activity against Matrix metalloproteinase-1 (MMP-1).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264845(CHEMBL4095552)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192804(CHEMBL3933401)copy SMILEScopy InChI
Affinity DataIC50: 0.570nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetStromelysin-1(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063915((2R,3S)-N*4*-Hydroxy-2-isobutyl-3-methyl-N*1*-[(S)...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Activity against Matrix metalloproteinase-3 (MMP-3).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50256212(CHEMBL4060956)copy SMILEScopy InChI
Affinity DataIC50: 0.620nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264848(CHEMBL4062935)copy SMILEScopy InChI
Affinity DataIC50: 0.650nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetStromelysin-1(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063918((2R,3S)-N*4*-Hydroxy-2-isobutyl-N*1*-((S)-1-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.650nMAssay Description:Activity against Matrix metalloproteinase-3 (MMP-3).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264857(CHEMBL4090714)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of hypotonicity-induced activation pretreated for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264856(CHEMBL4084992)copy SMILEScopy InChI
Affinity DataIC50: 0.870nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192820(CHEMBL3950646)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063921((2R,3S)-N*1*-((S)-Cyclohexyl-methylcarbamoyl-methy...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50256230(CHEMBL4083772)copy SMILEScopy InChI
Affinity DataIC50: 0.970nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264855(CHEMBL4091558)copy SMILEScopy InChI
Affinity DataIC50: 0.990nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192808(CHEMBL3915150)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063918((2R,3S)-N*4*-Hydroxy-2-isobutyl-N*1*-((S)-1-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Activity against Matrix metalloproteinase-2 (MMP-2).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Activity against Matrix metalloproteinase-2 (MMP-2).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192779(CHEMBL3957347)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50256210(CHEMBL4080527)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of 4alphaPDD-induced activation pretreated for 5 mins ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50264844(CHEMBL4069724)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of hypotonicity-induced activation pretreated for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063910((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Activity against Matrix metalloproteinase-9 (MMP-9).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50263440(CHEMBL4083195)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Antagonist activity at recombinant human TRPV4 expressed in CHOK1 cells assessed as inhibition of hypotonicity-induced activation pretreated for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PT9PubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Activity against Matrix metalloproteinase-1 (MMP-1).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Kanebo Ltd.

Curated by ChEMBL
LigandPNGBDBM50063912((R)-N*4*-Hydroxy-N*1*-((S)-methylcarbamoyl-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Activity against Matrix metalloproteinase-2 (MMP-2).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ8ZHBPubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Shionogi& Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50192817(CHEMBL3924485)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Antagonist activity at human TRPV4 assessed as inhibition of 4alpha-PDD-induced activationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154K06PubMed
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