Amprenavir

Amprenavir

SCHEMBL7287657

CC(C)CN(CC(O)C(Cc1ccccc1)NC(=O)OC1CCOC1)S(=O)(=O)c1ccc(N)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

The experimentally established mechanism targets of Amprenavir. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MLNR O43193 1/20 1.00
ABCB11 O95342 1/20 1.00
LMNA P02545 1/20 1.00
CTSD P07339 1/20 1.00
CYP3A4 P08684 1/20 1.00
CYP3A5 P20815 1/20 1.00
CNR1 P21554 1/20 1.00
TBXAS1 P24557 1/20 1.00
ADRA1A P35348 1/20 1.00
ABCB1 P08183 1/20 0.72
KCNE1 P15382 1/20 0.72
KCNQ1 P51787 1/20 0.72
KCNH2 Q12809 1/20 0.72
SCN5A Q14524 1/20 0.72
KCND3 Q9UK17 1/20 0.72

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Amprenavir SCHEMBL11914014 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL1388821 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL20099148 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL5551513 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL3174937 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL34151 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL2671137 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL10276771 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL20451345 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4
Amprenavir SCHEMBL12647024 1.00 MLNR (1.00) MLNRABCB11LMNACTSDCYP3A4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0977570-A1 QUINOXALINE IN TRIPLE COMBINATION WITH PROTEASE INHIBITORS AND REVERSE TRANSCRIPTASE INHIBITORS AS MEDICINES FOR TREATING AIDS BAYER AG (DE) 2000-02-09 EP claimed
WO-1998032442-A1 QUINOXALINE IN TRIPLE COMBINATION WITH PROTEASE INHIBITORS AND REVERSE TRANSCRIPTASE INHIBITORS AS MEDICINES FOR TREATING AIDS BAYER AKTIENGESELLSCHAFT (DE) 1998-07-30 WO claimed
EP-0728481-A2 Use of quinoxaline and protease inhibitors in a composition for the treatment of AIDS and/or HIV infections BAYER AG (DE) 1996-08-28 EP claimed
US-9107956-B2 Oligomer-protease inhibitor conjugates NEKTAR THERAPEUTICS (US) 2015-08-18 US disclosed
EP-2830629-A1 COMPOSITIONS AND METHODS FOR REACTIVATING LATENT IMMUNODEFICIENCY VIRUS Icahn School of Medicine Mount Sinai (US) 2015-02-04 EP disclosed
US-20140045770-A1 OLIGOMER-PROTEASE INHIBITOR CONJUGATES NEKTAR THERAPEUTICS (US) 2014-02-13 US disclosed
WO-2013148197-A1 COMPOSITIONS AND METHODS FOR REACTIVATING LATENT IMMUNODEFICIENCY VIRUS THE J. DAVID GLADSTONE INSTITUTES (US) 2013-10-03 WO disclosed
US-20120108501-A1 Protease Inhibitors NEKTAR THERAPEUTICS (US) 2012-05-03 US disclosed
US-20110269677-A1 Oligomer-Protease Inhibitor Conjugates NEKTAR THERAPEUTICS (US) 2011-11-03 US disclosed
US-20100124543-A1 SULPHONAMIDE DERIVATIVES AS PRODRUGS OF ASPARTYL PROTEASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2010-05-20 US disclosed
US-20100124543-A1 SULPHONAMIDE DERIVATIVES AS PRODRUGS OF ASPARTYL PROTEASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2010-05-20 US disclosed
US-7592368-B2 Sulphonamide derivatives as prodrugs of aspartyl protease inhibitors VERTEX PHARMACEUTICALS INCORPORATED (US) 2009-09-22 US disclosed
US-7592368-B2 Sulphonamide derivatives as prodrugs of aspartyl protease inhibitors VERTEX PHARMACEUTICALS INCORPORATED (US) 2009-09-22 US disclosed
US-20070009593-A1 Methods of treating cancer Indianan University Advanced Research 2007-01-11 US disclosed
US-20070009593-A1 Methods of treating cancer Indianan University Advanced Research 2007-01-11 US disclosed
EP-0977570-A1 QUINOXALINE IN TRIPLE COMBINATION WITH PROTEASE INHIBITORS AND REVERSE TRANSCRIPTASE INHIBITORS AS MEDICINES FOR TREATING AIDS BAYER AG (DE) 2000-02-09 EP disclosed
WO-1998032442-A1 QUINOXALINE IN TRIPLE COMBINATION WITH PROTEASE INHIBITORS AND REVERSE TRANSCRIPTASE INHIBITORS AS MEDICINES FOR TREATING AIDS BAYER AKTIENGESELLSCHAFT (DE) 1998-07-30 WO disclosed
EP-0728481-A2 Use of quinoxaline and protease inhibitors in a composition for the treatment of AIDS and/or HIV infections BAYER AG (DE) 1996-08-28 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070009593-A1 Methods of treating cancer CAPN2, CAPN9, CAPN1 MLNR 3440/4885ABCB11 3462/4885LMNA 1278/4885
US-20100124543-A1 SULPHONAMIDE DERIVATIVES AS PRODRUGS OF ASPARTYL PROTEASE INHIBITORS PRSS1, TMPRSS15, SI MLNR 2865/4885ABCB11 549/4885LMNA 3813/4885
US-20120108501-A1 Protease Inhibitors DNPEP, ADAM17, PREP MLNR 692/4885ABCB11 658/4885LMNA 2367/4885
US-20140045770-A1 OLIGOMER-PROTEASE INHIBITOR CONJUGATES DNPEP, ADAM17, SERPINB1 MLNR 302/4885ABCB11 373/4885LMNA 4161/4885
US-20110269677-A1 Oligomer-Protease Inhibitor Conjugates ADAM17, DNPEP, SERPINB1 MLNR 411/4885ABCB11 799/4885LMNA 3409/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.