Compile Data Set for Download or QSAR
Report error Found 127 with Last Name = 'toth' and Initial = 'mv'
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011680(Qua-Asn-Phe-HEA(S)-Pro-Ile-Phe-OMe | CHEMBL3351098)
Affinity DataIC50: 2.30nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011684(Cbz-Asn-Phe-HEA(S)-Pro-Ile-Phe-OMe | CHEMBL3350878)
Affinity DataIC50: 4nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010495(Acetyl-Ser-Leu-Asn-Phe-[CH(OH)CH2N]Pro-Ile-Val-OMe...)
Affinity DataIC50: 9nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011682(BDBM50407039 | Ac-Ser-Leu-Asn-Phe-HEA(S)-Pro-O-ter...)
Affinity DataIC50: 14nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011687(Ac-Ser-Leu-Asn-Phe-HEA(R)-Pro-O-terbutyl | CHEMBL3...)
Affinity DataIC50: 14nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011688(Boc-Asn-Phe-HEA(R)-Pro-Ile-Val-OMe | CHEMBL3349554)
Affinity DataIC50: 16nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50005687(1-[3-(2-Benzyloxycarbonylamino-3-carbamoyl-propion...)
Affinity DataIC50: 51nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062142(4,6-Dimethyl-piperidin-(2Z)-ylideneamine | CHEMBL2...)
Affinity DataIC50: 60nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(CHEMBL109500 | Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)C...)
Affinity DataIC50: 65nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(CHEMBL109500 | Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)C...)
Affinity DataIC50: 65nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062142(4,6-Dimethyl-piperidin-(2Z)-ylideneamine | CHEMBL2...)
Affinity DataIC50: 80nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2Z)-ylideneamine | 4-Methyl-pi...)
Affinity DataIC50: 100nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50005687(1-[3-(2-Benzyloxycarbonylamino-3-carbamoyl-propion...)
Affinity DataIC50: 140nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104649(7-(2-Nitro-ethyl)-azepan-(2Z)-ylideneamine | CHEMB...)
Affinity DataIC50: 152nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2Z)-ylideneamine | 4-Methyl-pi...)
Affinity DataIC50: 200nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062132(6-Propyl-piperidin-(2Z)-ylideneamine | CHEMBL6760)
Affinity DataIC50: 200nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010500(CHEMBL113062 | 1-[3-(2-Benzyloxycarbonylamino-3-ca...)
Affinity DataIC50: 300nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062142(4,6-Dimethyl-piperidin-(2Z)-ylideneamine | CHEMBL2...)
Affinity DataIC50: 300nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104649(7-(2-Nitro-ethyl)-azepan-(2Z)-ylideneamine | CHEMB...)
Affinity DataIC50: 339nMAssay Description:Inhibitory activity against Neuronal nitric oxide synthase at 100 uM concentration was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062137(6-Methyl-piperidin-(2Z)-ylideneamine | CHEMBL26567...)
Affinity DataIC50: 400nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010500(CHEMBL113062 | 1-[3-(2-Benzyloxycarbonylamino-3-ca...)
Affinity DataIC50: 450nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062132(6-Propyl-piperidin-(2Z)-ylideneamine | CHEMBL6760)
Affinity DataIC50: 500nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062131(6-Trifluoromethyl-piperidin-(2Z)-ylideneamine | CH...)
Affinity DataIC50: 500nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062137(6-Methyl-piperidin-(2Z)-ylideneamine | CHEMBL26567...)
Affinity DataIC50: 500nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062131(6-Trifluoromethyl-piperidin-(2Z)-ylideneamine | CH...)
Affinity DataIC50: 500nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50064011(CHEMBL543514 | CHEMBL89288 | 7-Butyl-azepan-(2Z)-y...)
Affinity DataIC50: 517nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062137(6-Methyl-piperidin-(2Z)-ylideneamine | CHEMBL26567...)
Affinity DataIC50: 600nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062145(3-Methyl-piperidin-(2Z)-ylideneamine | CHEMBL26716...)
Affinity DataIC50: 700nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104654(2-(2-Amino-ethyl)-7-imino-azepane | CHEMBL92475)
Affinity DataIC50: 701nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011683(CHEMBL3349553 | Boc-Asn-Phe-HEA(S)-Pro-Ile-Val-OMe)
Affinity DataIC50: 850nMAssay Description:In vitro concentration required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50064011(CHEMBL543514 | CHEMBL89288 | 7-Butyl-azepan-(2Z)-y...)
Affinity DataIC50: 850nMAssay Description:Inhibitory activity against Neuronal nitric oxide synthase at 100 uM concentration was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104655(((E)-7-But-2-enyl)-azepan-(2Z)-ylideneamine | CHEM...)
Affinity DataIC50: 890nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062136(6-Benzyl-piperidin-(2Z)-ylideneamine | CHEMBL6875)
Affinity DataIC50: 900nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104654(2-(2-Amino-ethyl)-7-imino-azepane | CHEMBL92475)
Affinity DataIC50: 932nMAssay Description:Inhibitory activity against Neuronal nitric oxide synthase at 100 uM concentration was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104648(3-(2-Nitro-ethyl)-[1,4]oxazepan-(5Z)-ylideneamine ...)
Affinity DataIC50: 979nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2Z)-ylideneamine | 4-Methyl-pi...)
Affinity DataIC50: 1.10E+3nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049255(Piperidin-(2E)-ylideneamine | Piperidin-(2Z)-ylide...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049255(Piperidin-(2E)-ylideneamine | Piperidin-(2Z)-ylide...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062135(4-Ethyl-piperidin-(2Z)-ylideneamine | CHEMBL6813)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062131(6-Trifluoromethyl-piperidin-(2Z)-ylideneamine | CH...)
Affinity DataIC50: 2.00E+3nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049257(CHEMBL543752 | CHEMBL315857 | Azepan-(2Z)-ylidenea...)
Affinity DataIC50: 2.06E+3nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062132(6-Propyl-piperidin-(2Z)-ylideneamine | CHEMBL6760)
Affinity DataIC50: 2.20E+3nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104656(3-Butyl-[1,4]oxazepan-(5Z)-ylideneamine | CHEMBL89...)
Affinity DataIC50: 2.43E+3nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062135(4-Ethyl-piperidin-(2Z)-ylideneamine | CHEMBL6813)
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104653([1,4]Thiazepan-(5Z)-ylideneamine | [1,4]Thiazepan-...)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104649(7-(2-Nitro-ethyl)-azepan-(2Z)-ylideneamine | CHEMB...)
Affinity DataIC50: 2.77E+3nMAssay Description:Inhibition of endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062145(3-Methyl-piperidin-(2Z)-ylideneamine | CHEMBL26716...)
Affinity DataIC50: 3.00E+3nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062138(4-Trifluoromethyl-piperidin-(2Z)-ylideneamine | CH...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062138(4-Trifluoromethyl-piperidin-(2Z)-ylideneamine | CH...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50104655(((E)-7-But-2-enyl)-azepan-(2Z)-ylideneamine | CHEM...)
Affinity DataIC50: 3.39E+3nMAssay Description:Inhibitory activity against Neuronal nitric oxide synthase at 100 uM concentration was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Displayed 1 to 50 (of 127 total ) | Next | Last >>
Jump to: