Ciluprevir

Ciluprevir

SCHEMBL1735179

COc1ccc2c(O[C@@H]3C[C@H]4C(=O)N[C@]5(C(=O)O)CC5/C=C\CCCCC[C@H](NC(=O)OC5CCCC5)C(=O)N4C3)cc(-c3csc(NC(C)C)n3)nc2c1

nearest known ligand 0.75

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NS3NS4A

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ ADRB3 P13945 1/20 0.75
▸ ADRA2B P18089 1/20 0.75
▸ ADRA2C P18825 1/20 0.75
▸ CTSB P07858 2/20 0.45
▸ CTSS P25774 1/20 0.38
▸ PPP3CB P16298 1/20 0.38
▸ ABCC1 P33527 1/20 0.34
▸ ABCC2 Q92887 1/20 0.34
▸ ABCG2 Q9UNQ0 1/20 0.34
▸ CYP3A4 P08684 2/20 0.34

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
Ciluprevir SCHEMBL1736294 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL12300089 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL16199312 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL5152276 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL18671856 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL5152261 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL16438974 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
Ciluprevir SCHEMBL2524642 1.00 ADRB3 (0.75) ADRB3ADRA2BADRA2CCTSBCTSS
SCHEMBL13915576 0.96 ADRB3 (0.70) ADRB3ADRA2BADRA2CCTSBCTSS
SCHEMBL12154816 0.96 ADRB3 (0.69) ADRB3ADRA2BADRA2CCTSBCTSS

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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060068007-A1 Class of surfactant-like materials BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2006-03-30 — — US claimed
US-20230241026-A1 NOVEL DRUG-CONTROLLED SYSTEMS AND USES THEREOF TRUSTEES OF BOSTON UNIVERSITY (US) 2023-08-03 — — US disclosed
US-11660288-B2 Drug-controlled systems and uses thereof TRUSTEES OF BOSTON UNIVERSITY (US) 2023-05-30 — — US disclosed
US-20230159600-A1 REGULATED SYNTHETIC GENE EXPRESSION SYSTEMS TRUSTEES OF BOSTON UNIVERSITY (US) 2023-05-25 — — US disclosed
US-11572565-B2 Inducible control of gene expression TRUSTEES OF BOSTON UNIVERSITY (US) 2023-02-07 — — US disclosed
US-11530246-B2 Regulated synthetic gene expression systems TRUSTEES OF BOSTON UNIVERSITY (US) 2022-12-20 — — US disclosed
US-20220025381-A1 INDUCIBLE CONTROL OF GENE EXPRESSION TRUSTEES OF BOSTON UNIVERSITY (US) 2022-01-27 — — US disclosed
US-11059864-B2 Chimeric antigen receptor (CAR) modulation TRUSTEES OF BOSTON UNIVERSITY (US) 2021-07-13 — — US disclosed
US-20200377564-A1 REGULATED SYNTHETIC GENE EXPRESSION SYSTEMS TRUSTEES OF BOSTON UNIVERSITY (US) 2020-12-03 — — US disclosed
US-20200308234-A1 CHIMERIC ANTIGEN RECEPTOR (CAR) MODULATION TRUSTEES OF BOSTON UNIVERSITY (US) 2020-10-01 — — US disclosed
US-7429565-B2 Antiviral phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-09-30 — — US disclosed
US-20070237818-A1 Controlled-release formulation of HCV protease inhibitor and methods using the same SCHERING CORPORATION 2007-10-11 — — US disclosed
US-20070237818-A1 Controlled-release formulation of HCV protease inhibitor and methods using the same SCHERING CORPORATION 2007-10-11 — — US disclosed
US-20070021351-A1 Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor SCHERING CORPORATION 2007-01-25 — — US disclosed
US-20070021351-A1 Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor SCHERING CORPORATION 2007-01-25 — — US disclosed
US-20070004635-A1 Method of treating interferon non-responders using HCV protease inhibitor SCHERING CORPORATION 2007-01-04 — — US disclosed
US-20070004635-A1 Method of treating interferon non-responders using HCV protease inhibitor SCHERING CORPORATION 2007-01-04 — — US disclosed
US-20060068007-A1 Class of surfactant-like materials BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2006-03-30 — — US disclosed
US-20040229777-A1 Crystalline phases of a potent HCV inhibitor BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2004-11-18 — — US disclosed
WO-2004087741-A1 CRYSTALLINE PHASES OF A POTENT HCV INHIBITOR BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2004-10-14 — — WO 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 (12 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-11059864-B2 Chimeric antigen receptor (CAR) modulation HAVCR2, CPB1, CTRL ADRB3 3737/4885ADRA2B 3371/4885ADRA2C 3962/4885
US-20230159600-A1 REGULATED SYNTHETIC GENE EXPRESSION SYSTEMS SRRT, BPTF, MYCBP ADRB3 4589/4885ADRA2B 4590/4885ADRA2C 4561/4885
US-20040229777-A1 Crystalline phases of a potent HCV inhibitor HAVCR2, HCCS, PYGL ADRB3 4221/4885ADRA2B 4321/4885ADRA2C 3824/4885
US-20070004635-A1 Method of treating interferon non-responders using HCV protease inhibitor IFNAR1, IFNG, IRF3 ADRB3 1837/4885ADRA2B 2016/4885ADRA2C 2396/4885
US-11660288-B2 Drug-controlled systems and uses thereof ATF4, MRPL21, SARS1 ADRB3 1925/4885ADRA2B 2727/4885ADRA2C 2803/4885
US-20230241026-A1 NOVEL DRUG-CONTROLLED SYSTEMS AND USES THEREOF ATF4, MRPL21, TMPRSS2 ADRB3 1423/4885ADRA2B 1976/4885ADRA2C 1911/4885
US-20060068007-A1 Class of surfactant-like materials SMURF1, SMURF2, EBPL ADRB3 3350/4885ADRA2B 3720/4885ADRA2C 3936/4885
US-11530246-B2 Regulated synthetic gene expression systems SRRT, BPTF, MYCBP ADRB3 4589/4885ADRA2B 4590/4885ADRA2C 4561/4885
US-20200308234-A1 CHIMERIC ANTIGEN RECEPTOR (CAR) MODULATION HAVCR2, CPB1, CTRL ADRB3 3737/4885ADRA2B 3371/4885ADRA2C 3962/4885
US-20070021351-A1 Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor PYGL, SERPINB1, PREP ADRB3 4070/4885ADRA2B 4543/4885ADRA2C 4304/4885
US-20200377564-A1 REGULATED SYNTHETIC GENE EXPRESSION SYSTEMS SRRT, BPTF, MYCBP ADRB3 4589/4885ADRA2B 4590/4885ADRA2C 4561/4885
US-20070237818-A1 Controlled-release formulation of HCV protease inhibitor and methods using the same CTRL, PEPD, PRCP ADRB3 3161/4885ADRA2B 2445/4885ADRA2C 3215/4885

“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.

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