SCHEMBL329193

SCHEMBL329193

CCC[C@H](N)C(O)C(=O)NC1CC1

nearest known ligand 0.43

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SMYD3 Q9H7B4 1/20 0.43
METAP1 P53582 3/20 0.41
METAP2 P50579 9/20 0.40
LMNA P02545 1/20 0.40
BLM P54132 1/20 0.40
KMT2A Q03164 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
SIGMAR1 Q99720 1/20 0.37
MME P08473 1/20 0.36
ANPEP P15144 1/20 0.36
DNPEP Q9ULA0 1/20 0.36
GPR88 Q9GZN0 1/20 0.35

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
SCHEMBL3045972 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
SCHEMBL328991 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
SCHEMBL13058644 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
SCHEMBL2331995 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
SCHEMBL13201892 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
SCHEMBL329101 1.00 SMYD3 (0.43) SMYD3METAP1METAP2LMNABLM
Hydrochloric Acid SCHEMBL4205427 0.98 SMYD3 (0.42) SMYD3METAP1METAP2LMNABLM
Hydrochloric Acid SCHEMBL329085 0.98 SMYD3 (0.42) SMYD3METAP1METAP2LMNABLM
Hydrochloric Acid SCHEMBL329165 0.98 SMYD3 (0.42) SMYD3METAP1METAP2LMNABLM
Hydrochloric Acid SCHEMBL29618100 0.98 SMYD3 (0.42) SMYD3METAP1METAP2LMNABLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105085310-A New synthesis method of telaprevir intermediate CHONGQING HUIZHI PHARMACEUTICAL RES INST CO LTD 2015-11-25 CN claimed
WO-2014203208-A1 PROCESS FOR THE PREPARATION OF TELAPREVIR AND INTERMEDIATES THEREOF RANBAXY LABORATORIES LIMITED (IN) 2014-12-24 WO claimed
WO-2014083582-A2 NOVEL PROCESS FOR THE PREPARATION OF (1S,3AR,6AS)-2-[(2S)-2-({(2S)-2-CYCLOHEXYL-2-[(PYRAZIN-2-YLCARBONYL)AMINO]ACETYL}AMINO)-3,3-DIMETHYLBUTANOYL]-N-[(3S)-1-(CYCLOPROPYLAMINO)-1,2-DIOXOHEXAN-3-YL]-3,3A,4,5,6,6A-HEXAHYDRO-1H-CYCLOPENTA[C] PYRROLE-1-CARBOXAMIDE AND ITS INTERMEDIATES MSN LABORATORIES LIMITED (IN) 2014-06-05 WO claimed
WO-2013136265-A1 SYNTHESIS OF AN INTERMEDIATE OF AN ANTIVIRAL COMPOUND DIPHARMA FRANCIS S.R.L. (IT) 2013-09-19 WO claimed
US-20210338825-A1 DEGRADERS OF HEPATITIS C VIRUS NS3/4A PROTEIN DANA-FARBER CANCER INSTITUTE, INC. (US) 2021-11-04 US disclosed
WO-2020069125-A1 DEGRADERS OF HEPATITIS C VIRUS NS3/4A PROTEIN DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-04-02 WO disclosed
CN-105085310-B New synthesis method of telaprevir intermediate 重庆汇智药物研究院有限公司 2017-05-10 CN disclosed
EP-1919478-B1 COMBINATION OF HCV PROTEASE INHIBITORS WITH A SURFACTANT MERCK SHARP & DOHME (US) 2016-03-23 EP disclosed
CN-105085310-A New synthesis method of telaprevir intermediate CHONGQING HUIZHI PHARMACEUTICAL RES INST CO LTD 2015-11-25 CN disclosed
CN-105085310-A New synthesis method of telaprevir intermediate CHONGQING HUIZHI PHARMACEUTICAL RES INST CO LTD 2015-11-25 CN disclosed
CN-104860897-A Intermediate for preparing N-cyclopropyl-(2S, 3S)-3-amino-2-hydroxy caproamide, preparation method and applications thereof SHANGHAI DESANO CHEMICAL PHARM 2015-08-26 CN disclosed
EP-1906945-B1 HCV INHIBITORS VIROBAY INC (US) 2015-08-05 EP disclosed
WO-2006130666-A2 MEDICAMENTS AND METHODS COMBINING A HCV PROTEASE INHIBITOR AND AN AKR COMPETITOR SCHERING CORPORATION (US) 2006-12-07 WO disclosed
WO-2006130607-A2 CONTROLLED-RELEASE FORMULATION USEFUL FOR TREATING DISORDERS ASSOCIATED WITH HEPATITIS C VIRUS SCHERING CORPORATION (US) 2006-12-07 WO disclosed
WO-2005007681-A9 INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE 2006-04-06 WO disclosed
WO-2005035525-A2 2-AMIDO-4-ARYLOXY-1-CARBONYLPYRROLIDINE DERIVATIVES AS INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-04-21 WO disclosed
WO-2005028502-A1 INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE VERTEX PHARMACEUTICALS, INCORPORATED (US) 2005-03-31 WO disclosed
WO-2005007681-A2 INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-01-27 WO disclosed
WO-2003035060-A1 INHIBITORS OF SERINE PROTEASE, PARTICULARLY HEPATITIS C VIRUS NS3-NS4A PROTEASE, INCORPORATING A FUSED RING SYSTEM VERTEX PHARMACEUTICALS INCORPORATED (US) 2003-05-01 WO disclosed
WO-2003006490-A1 BRIDGED BICYCLIC SERINE PROTEASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2003-01-23 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 (1 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-20210338825-A1 DEGRADERS OF HEPATITIS C VIRUS NS3/4A PROTEIN HAVCR2, CUL4A, PSMC3 SMYD3 3728/4885METAP1 385/4885METAP2 622/4885

“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.