BindingDB PrimarySearch

Found 752 of ic50 data for polymerid = 7501

Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50485288(CHEMBL2046980)

IC50: 0.00150nMAssay Description:Inhibition of HIV1 3B protease activity in human H9 cells using Abz-Thr-Ile-Nle-Phe(p-NO2)-Gln-Arg-NH2 as substrate after 40 mins by spectrophotometr...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482331(CHEMBL1170704)

IC50: 0.00700nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50280116(CHEMBL4177355)

IC50: 0.0120nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli using Val-Ser-Gln-Asn-(beta-naphtyl)Ala-Pro-Ile-Val as substrate preincubated for 30 mins f...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

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

IC50: 0.0130nMAssay Description:Inhibition of GAR transformylase from Lactobacillus caseiMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482336(CHEMBL1170709)

IC50: 0.0130nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482332(CHEMBL1170706)

IC50: 0.0160nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50127975((R)-3-[(2S,4R)-2-Hydroxy-4-((3S,4S)-3-hydroxy-chro...)

IC50: 0.0300nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482337(CHEMBL1170703)

IC50: 0.0300nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM13934(Atazanavir | BMS 232632 | CGP 73547 | CHEMBL1163 |...)

IC50: 0.0400nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli using Val-Ser-Gln-Asn-(beta-naphtyl)Ala-Pro-Ile-Val as substrate preincubated for 30 mins f...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM13934(Atazanavir | BMS 232632 | CGP 73547 | CHEMBL1163 |...)

IC50: 0.0400nMAssay Description:Inhibition of wild-type HIV1 protease expressed in Escherichia coli assessed as reduction in product formation preincubated for 30 mins followed by a...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497089(CHEMBL3263091)

IC50: 0.0500nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

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

IC50: 0.0600nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli using Arg-Glu (EDANS)-Ser-GlnAsn-Tyr-Pro-Ile-Val-Gln-Lys(DABCYL)-Arg as substrate preincuba...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

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

IC50: 0.0610nMT: 2°CAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli incubated for 20 to 30 mins at room temperature using (Arg-Glu(EDANS)-Ser-Gln-Asn-Tyr-Pro-I...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478722(CHEMBL452953 | KNI-1933)

IC50: 0.0830nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478719(CHEMBL509400 | KNI-1965)

IC50: 0.0860nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478712(CHEMBL485911 | KNI-1969)

IC50: 0.0900nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478713(CHEMBL510136 | KNI-1961)

IC50: 0.0900nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477640(CHEMBL247616)

IC50: 0.100nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482333(CHEMBL1170707)

IC50: 0.100nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477633(CHEMBL398053)

IC50: 0.100nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497086(CHEMBL3263090)

IC50: 0.100nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482334(CHEMBL1170708)

IC50: 0.100nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477636(CHEMBL395214)

IC50: 0.110nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497088(CHEMBL3263089)

IC50: 0.110nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478715(CHEMBL452873 | KNI-1910)

IC50: 0.110nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497090(CHEMBL3263092)

IC50: 0.120nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477638(CHEMBL397403)

IC50: 0.140nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477635(CHEMBL247615)

IC50: 0.170nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50485183(CHEMBL2034991)

IC50: 0.170nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478721(CHEMBL230484 | KNI-1931)

IC50: 0.180nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50477634(CHEMBL395207)

IC50: 0.200nMAssay Description:Inhibition of wild type HIV1 NL4-3 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478714(CHEMBL462726 | KNI-1909)

IC50: 0.220nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478718(CHEMBL455816 | KNI-1932)

IC50: 0.260nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478720(CHEMBL508278 | KNI-1960)

IC50: 0.270nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM13934(Atazanavir | BMS 232632 | CGP 73547 | CHEMBL1163 |...)

IC50: 0.300nMAssay Description:Inhibition of HIV1 protease activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481036(CHEMBL568589)

IC50: 0.302nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481029(CHEMBL569671)

IC50: 0.302nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481028(CHEMBL566620)

IC50: 0.302nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481018(CHEMBL568883)

IC50: 0.302nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481014(CHEMBL568951)

IC50: 0.339nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50270566(CHEMBL4129828)

IC50: 0.350nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli using Arg-Glu (EDANS)-Ser-GlnAsn-Tyr-Pro-Ile-Val-Gln-Lys(DABCYL)-Arg as substrate preincuba...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497087(CHEMBL3263094)

IC50: 0.360nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50478716(CHEMBL449836 | KNI-1878)

IC50: 0.390nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481023(CHEMBL566849)

IC50: 0.398nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50481020(CHEMBL565964)

IC50: 0.398nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibition of enzyme activityMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50482338(CHEMBL1170705)

IC50: 0.400nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50067593(CHEBI:44032 | Crixivan | Indinavir | L-735524 | MK...)

IC50: 0.400nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50213021(CHEBI:63621 | Fortovase | Invirase | Ro-31-8959 | ...)

IC50: 0.400nMAssay Description:Inhibition of recombinant wild type HIV1 protease assessed as hydrolysis of fluorogenic substrateMore data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

BDBM50497085(CHEMBL3263093)

IC50: 0.430nMAssay Description:Inhibition of purified HIV-1 protease using [Arg-Glu(EDANS)-Ser-Gin-Asn-Tyr-Ile-Val-Gin-Lys(dabcyl)-Arg) as fluorogenic substrate by fluorescence ass...More data for this Ligand-Target Pair

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Protease(Human immunodeficiency virus 1 (HIV-1))
University Of Trieste

Curated by ChEMBL

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

IC50: 0.460nMAssay Description:Inhibition of HIV1 protease expressed in Escherichia coli using Arg-Glu (EDANS)-Ser-Gln-Asn-Tyr-Pro-Ile-Val-Gln-Lys(DABCYL)-Arg as substrate preincub...More data for this Ligand-Target Pair

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3D Structure (crystal)

Displayed 1 to 50 (of 752 total ) | Next | Last >>

Filter my 752 hits

Targets 1▿
- Protease 752
Publications 50▿
- J Nat Prod 82: 2886-2896 (2019) 122
- Bioorg Med Chem Lett 25: 1880-3 (2015) 50
- Eur J Med Chem 137: 30-44 (2017) 49
- Bioorg Med Chem Lett 24: 2465-8 (2014) 37
- Bioorg Med Chem Lett 29: 1541-1545 (2019) 34
- Eur J Med Chem 44: 4344-52 (2009) 31
- Eur J Med Chem 185: (2020) 25
- Eur J Med Chem 74: 278-301 (2014) 25
- Bioorg Med Chem Lett 29: 357-361 (2019) 22
- ACS Med Chem Lett 7: 702-7 (2016) 21
- Bioorg Med Chem 17: 3003-10 (2009) 20
- J Med Chem 55: 3900-10 (2012) 16
- J Med Chem 59: 2849-78 (2016) 15
- Bioorg Med Chem 17: 967-76 (2009) 14
- Eur J Med Chem 53: 13-21 (2012) 13
- J Med Chem 62: 3553-3574 (2019) 13
- J Med Chem 53: 1451-7 (2010) 12
- J Med Chem 51: 2992-3004 (2008) 11
- Bioorg Med Chem 21: 1964-71 (2013) 11
- J Nat Prod 63: 238-42 (2000) 11
- Bioorg Med Chem Lett 17: 5432-6 (2007) 11
- J Med Chem 55: 10130-5 (2012) 10
- Bioorg Med Chem Lett 19: 6023-6 (2009) 10
- Bioorg Med Chem Lett 21: 2274-7 (2011) 10
- Bioorg Med Chem 17: 3671-9 (2009) 9
- J Nat Prod 71: 1022-6 (2008) 9
- Bioorg Med Chem 17: 5238-46 (2009) 8
- J Med Chem 62: 9375-9414 (2019) 8
- Bioorg Med Chem Lett 20: 4065-8 (2010) 8
- J Nat Prod 56: 755-61 (1993) 7
- J Nat Prod 55: 1170-7 (1992) 6
- Bioorg Med Chem Lett 17: 5614-9 (2007) 6
- Eur J Med Chem 84: 444-53 (2014) 6
- Bioorg Med Chem Lett 18: 5406-10 (2008) 6
- Bioorg Med Chem Lett 22: 2948-50 (2012) 6
- ACS Med Chem Lett 2: 461-5 (2011) 5
- J Nat Prod 72: 2019-23 (2009) 5
- Bioorg Med Chem 21: 7430-4 (2013) 4
- ACS Med Chem Lett 8: 1292-1297 (2017) 4
- US Patent US9085571 (2015) 3
- Eur J Med Chem 101: 409-18 (2015) 2
- Bioorg Med Chem 15: 7576-80 (2007) 2
- J Nat Prod 62: 1510-3 (1999) 2
- Eur J Med Chem 45: 4096-103 (2010) 2
- J Nat Prod 66: 729-31 (2003) 2
- J Med Chem 58: 5088-95 (2015) 2
- ACS Med Chem Lett 5: 968-72 (2014) 1
- Bioorg Med Chem 18: 2037-48 (2010) 1
- Eur J Med Chem 43: 1412-22 (2008) 1
- J Med Chem 63: 2751-2788 (2020) 1
- ...
Institutions 31▿
- TBA 135
- Chinese Academy Of Medical Science And Peking Union Medical College 130
- Shandong University 60
- Chinese Academy Of Medical Sciences And Peking Union Medical College 50
- Merck Research Laboratories 47
- University Of Toyama 34
- Universidade Federal De Lavras 31
- Universit£ 27
- Universidad De Granada 25
- University Of Kwazulu-Natal 23
- University Of Trieste 17
- Purdue University 17
- University Of Minnesota 13
- Rhodes University 11
- Toyama Medical And Pharmaceutical University 11
- Kyoto Pharmaceutical University 11
- New York University 10
- Academy Of Sciences Of The Czech Republic 10
- Osaka University Of Pharmaceutical Sciences 8
- Smithkline Beecham Pharmaceuticals 6
- University Of Florence 6
- University Of Southampton 5
- Wayne State University 4
- Merck 4
- Purdue Research Foundation 3
- Nankai University 2
- Teikyo University 2
- Beijing Medical University 2
- Beijing Institute Of Biotechnology 2
- Georgia State University 2
- Universidade Federal De Minas Gerais 1
- ...
Affinity: 0.0015 to 2.0E+6 nM▿
- Ki 3
- IC50 752
- Affinity ≤ nM
Xtal structures: 20
Docked structures: 0
Catalog Cmpds: 39