BindingDB PrimarySearch

Found 2615 with Last Name = 'pannecouque' and Initial = 'c'

Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

Ki: 0.00100nMAssay Description:Inhibition of HIV1 protease using RE(Edans)SGIFLETSK(Dabcyl)R as substrate by fluorescence methodMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)

Ki: 0.00800nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair

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3D Structure (crystal)

Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)

Ki: 0.0100nMAssay Description:Inhibition of HIV1 protease using RE(Edans)SGIFLETSK(Dabcyl)R as substrate by fluorescence methodMore data for this Ligand-Target Pair

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3D Structure (crystal)

Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 1.70nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 1.70nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 1.70nMAssay Description:Inhibition of HIV1 protease using Pr SF-2-WTQ7K-Pr as substrate after 24 hrs by LC/MS-MS analysisMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163750(CHEMBL3797292)

Ki: 4nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163750(CHEMBL3797292)

Ki: 4nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50200943(CHEMBL269769 | cyclopentyl (2S,3S)-3-[4-([4-(5-chl...)

Ki: 8nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair

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Sodium- and chloride-dependent GABA transporter 1(Rattus norvegicus)
Shandong University

Curated by ChEMBL

BDBM50505281(CHEMBL2315948)

Ki: 8.10nMAssay Description:Inhibition of NO711 binding to mouse GAT1 receptor expressed in HEK293 cell membranes incubated for 1 hr by LC-ESI-MS/MS analysisMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163750(CHEMBL3797292)

Ki: 9.70nMAssay Description:Inhibition of HIV1 protease G48V mutantMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 10nMAssay Description:Inhibition of HIV1 protease V82F mutantMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM2483((4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluor...)

Ki: 10nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163750(CHEMBL3797292)

Ki: 13nMAssay Description:Inhibition of HIV1 protease V82F mutantMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163752(CHEMBL3799500)

Ki: 16nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 22nMAssay Description:Inhibition of HIV1 protease G48V mutantMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163737(CHEMBL3799941)

Ki: 27nMAssay Description:Inhibition of HIV1 protease V82A mutantMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
Shandong University

Curated by ChEMBL

BDBM50163750(CHEMBL3797292)

Ki: 30nMAssay Description:Inhibition of HIV1 protease V82A mutantMore data for this Ligand-Target Pair

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Sodium- and chloride-dependent GABA transporter 1(Rattus norvegicus)
Shandong University

Curated by ChEMBL

BDBM50505274(CHEMBL2315639)

Ki: 117nMAssay Description:Inhibition of NO711 binding to mouse GAT1 receptor expressed in HEK293 cell membranes incubated for 1 hr by LC-ESI-MS/MS analysisMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484340(CHEMBL1835512)

Ki: 160nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484329(CHEMBL1835505)

Ki: 210nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490649(CHEMBL2337184)

Ki: 260nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490643(CHEMBL2337196)

Ki: 310nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490644(CHEMBL2337195)

Ki: 310nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484339(CHEMBL1835509)

Ki: 360nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484334(CHEMBL1835504)

Ki: 450nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484342(CHEMBL1835511)

Ki: 470nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484330(CHEMBL1835507)

Ki: 520nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490669(CHEMBL2337192)

Ki: 550nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484328(CHEMBL1835503)

Ki: 650nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490662(CHEMBL2337194)

Ki: 670nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484343(CHEMBL1835510)

Ki: 820nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490648(CHEMBL2337186)

Ki: 1.00E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490646(CHEMBL2337190)

Ki: 1.00E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490668(CHEMBL2337189)

Ki: 1.00E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484332(CHEMBL1835514)

Ki: 1.10E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484331(CHEMBL1835508)

Ki: 1.70E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484337(CHEMBL1835501)

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484324(CHEMBL1835515)

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484338(CHEMBL1835506)

Ki: 2.00E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484325(CHEMBL1835499)

Ki: 2.10E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484327(CHEMBL1835502)

Ki: 2.60E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484336(CHEMBL1835498)

Ki: 2.70E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484326(CHEMBL1835500)

Ki: 3.10E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50063002(CHEMBL3398101)

Ki: 4.50E+3nMAssay Description:Inhibition of HIV1 recombinant wild type reverse transcriptase p66/p51 pre-incubated with compound before enzyme addition using poly(rA) template and...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50484341(CHEMBL1835497)

Ki: 6.30E+3nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...More data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490660(CHEMBL2337187)

Ki: 6.50E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490642(CHEMBL2337197)

Ki: 6.60E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM50490665(CHEMBL2337181)

Ki: 6.60E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Reverse transcriptase(Human immunodeficiency virus 1)
Volgograd State Medical University

Curated by ChEMBL

BDBM1434(11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3...)

Ki: 7.20E+3nMAssay Description:Non-competitive inhibition of wild type HIV1 reverse transcriptase p66/p51 after 30 mins by liquid scintillation countingMore data for this Ligand-Target Pair

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Displayed 1 to 50 (of 2615 total ) | Next | Last >>

Filter my 2615 hits

Targets 32▿
- Reverse transcriptase 1510
- Reverse transcriptase/RNaseH 610
- Reverse transcriptase protein 97
- Integrase 79
- Protease 39
- Structural capsid protein 36
- Cytochrome P450 3A4 32
- Cytochrome P450 2D6 28
- Cytochrome P450 2C9 27
- Cytochrome P450 2C19 27
- Potassium voltage-gated channel subfamily H member 2 26
- Cytochrome P450 1A2 25
- Gag-Pol polyprotein [1148-1435] 20
- T-cell surface glycoprotein CD4 19
- Gag-Pol polyprotein [588-1027]/[588-1147] 9
- Envelope glycoprotein gp160 6
- Gag-Pol polyprotein 3
- Histone deacetylase 2
- Histone deacetylase 8 2
- Nuclear receptor corepressor 1 2
- Histone deacetylase 6 2
- Histone deacetylase 4 2
- Sodium- and chloride-dependent GABA transporter 1 2
- Histone deacetylase 1 2
- C-X-C chemokine receptor type 4 1
- Tyrosine-protein kinase JAK3 1
- Tyrosine-protein kinase JAK2 1
- Non-receptor tyrosine-protein kinase TYK2 1
- C-C chemokine receptor type 5 1
- Histone deacetylase 3 1
- Tyrosine-protein kinase JAK1 1
- cAMP-specific 3',5'-cyclic phosphodiesterase 4B 1
- ...
Publications 50▿
- J Med Chem 54: 1587-98 (2011) 128
- Bioorg Med Chem 25: 3861-3870 (2017) 122
- Eur J Med Chem 202: (2020) 118
- Eur J Med Chem 214: (2021) 95
- ACS Med Chem Lett 9: 370-375 (2018) 83
- Eur J Med Chem 226: (2021) 77
- Bioorg Med Chem 26: 661-674 (2018) 77
- Bioorg Med Chem 25: 2491-2497 (2017) 70
- Eur J Med Chem 240: (2022) 69
- J Med Chem 63: 4837-4848 (2020) 64
- Eur J Med Chem 238: (2022) 60
- J Med Chem 64: 5067-5081 (2021) 60
- J Med Chem 42: 1401-14 (1999) 54
- Bioorg Med Chem 18: 1702-10 (2010) 54
- J Med Chem 62: 9375-9414 (2019) 48
- J Med Chem 65: 8478-8492 (2022) 47
- J Med Chem 64: 13658-13675 (2021) 47
- J Med Chem 65: 2122-2138 (2022) 47
- J Med Chem 64: 10297-10311 (2021) 43
- J Med Chem 62: 1484-1501 (2019) 42
- Bioorg Med Chem 26: 2051-2060 (2018) 41
- J Med Chem 62: 2083-2098 (2019) 40
- Bioorg Med Chem Lett 14: 3173-6 (2004) 38
- J Med Chem 50: 4854-67 (2007) 37
- Bioorg Med Chem 22: 1459-67 (2014) 34
- Bioorg Med Chem 23: 1069-81 (2015) 32
- Bioorg Med Chem 21: 1150-8 (2013) 31
- J Med Chem 59: 2849-78 (2016) 29
- J Med Chem 65: 2458-2470 (2022) 26
- Eur J Med Chem 213: (2021) 26
- Bioorg Med Chem 16: 7429-35 (2008) 25
- J Med Chem 64: 13604-13621 (2021) 24
- Eur J Med Chem 155: 714-724 (2018) 24
- Bioorg Med Chem 27: 3836-3845 (2019) 24
- ACS Med Chem Lett 9: 334-338 (2018) 24
- Eur J Med Chem 145: 726-734 (2018) 24
- Eur J Med Chem 87: 52-62 (2014) 24
- Eur J Med Chem 121: 352-363 (2016) 23
- Bioorg Med Chem 17: 5962-7 (2009) 23
- Eur J Med Chem 240: (2022) 22
- Eur J Med Chem 225: (2021) 22
- Bioorg Med Chem 23: 6587-93 (2015) 22
- Eur J Med Chem 102: 215-22 (2015) 21
- Bioorg Med Chem 19: 5794-802 (2011) 21
- J Med Chem 48: 6140-55 (2005) 20
- Eur J Med Chem 93: 330-7 (2015) 20
- Chem Biol Drug Des 83: 154-66 (2014) 20
- J Med Chem 44: 703-14 (2001) 19
- Eur J Med Chem 65: 134-43 (2013) 18
- J Med Chem 63: 1298-1312 (2020) 17
Institutions 11▿
- Shandong University 765
- Universit£ 335
- Fudan University 298
- Sichuan University 178
- Yanbian University College Of Pharmacy 146
- Sapienza University Of Rome 128
- Wuhan Institute Of Technology 92
- Volgograd State Medical University 84
- Purdue University 76
- National Cancer Institute-Bethesda 54
- Nirma University 20
Affinity: 0.0010 to 5.2E+7 nM▿
- Ki 88
- IC50 2014
- Kd 37
- EC50 476
- Affinity ≤ nM
Xtal structures: 34
Docked structures: 3
Catalog Cmpds: 75