1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole and leupeptin

1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole has been researched along with leupeptin in 1 studies

Compound Research Comparison

Studies (1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole)	Trials (1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole)	Recent Studies (post-2010) (1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole)	Studies (leupeptin)	Trials (leupeptin)	Recent Studies (post-2010) (leupeptin)
13	0	3	944	0	74

Protein Interaction Comparison

Protein	Taxonomy	leupeptin (IC50)
Plasminogen	Homo sapiens (human)	1.2
Cationic trypsin	Bos taurus (cattle)	8.1
Trypsin	Sus scrofa (pig)	0.5
Papain	Carica papaya (papaya)	0.0022
Plasminogen	Bos taurus (cattle)	3.7
Trypsin-1	Homo sapiens (human)	0.6
Trypsin-2	Homo sapiens (human)	0.6
Cathepsin B	Bos taurus (cattle)	0.31
Procathepsin L	Homo sapiens (human)	0.0045
Cathepsin B	Homo sapiens (human)	0.0282
Trypsin-3	Homo sapiens (human)	0.6
Calpain-1 catalytic subunit	Sus scrofa (pig)	0.08
Cysteine protease	Leishmania donovani	0.01
Cysteine proteinase falcipain 2a	Plasmodium falciparum (malaria parasite P. falciparum)	0.0636
Cysteine protease falcipain-3	Plasmodium falciparum (malaria parasite P. falciparum)	0.0925

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Raghav, N; Singh, M	1

Other Studies

1 other study(ies) available for 1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole and leupeptin

Article	Year
SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H. Bioorganic & medicinal chemistry, 2014, Aug-01, Volume: 22, Issue:15 Topics: Animals; Binding Sites; Catalytic Domain; Cathepsin B; Cathepsin H; Chalcones; Cyclization; Humans; Hydrazones; Kinetics; Molecular Docking Simulation; Protease Inhibitors; Protein Binding; Structure-Activity Relationship	2014

Article

Year

SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H.

Bioorganic & medicinal chemistry, 2014, Aug-01, Volume: 22, Issue:15

Topics: Animals; Binding Sites; Catalytic Domain; Cathepsin B; Cathepsin H; Chalcones; Cyclization; Humans; Hydrazones; Kinetics; Molecular Docking Simulation; Protease Inhibitors; Protein Binding; Structure-Activity Relationship

2014