SCHEMBL1977030

SCHEMBL1977030

NC(=O)c1ccc(OCCCCl)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 7/20 0.68
PARP15 Q460N3 2/20 0.55
PARP4 Q9UKK3 2/20 0.55
ALDH1A1 P00352 1/20 0.55
KMT2A Q03164 1/20 0.55
PARP14 Q460N5 1/20 0.55
PARP16 Q8N5Y8 1/20 0.55
PARP11 Q9NR21 1/20 0.55
PARP2 Q9UGN5 2/20 0.54
PRSS1 P07477 3/20 0.53
TMPRSS2 O15393 2/20 0.53
L3MBTL1 Q9Y468 1/20 0.53
HRH3 Q9Y5N1 2/20 0.52
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
PARP1 P09874 1/20 0.52
PRMT1 Q99873 3/20 0.52
F2 P00734 2/20 0.52
ST14 Q9Y5Y6 2/20 0.52
PLAU P00749 1/20 0.52

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
SCHEMBL3082936 0.94 PARP10 (0.66) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL3085074 0.92 PARP10 (0.68) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL1787654 0.87 PARP10 (0.62) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL1086686 0.85 PARP10 (0.72) PARP10L3MBTL1GAA
Water SCHEMBL5055924 0.85 PARP10 (0.68) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL27987025 0.85 PARP10 (0.68) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL4687732 0.85 PARP10 (0.68) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL27972513 0.84 PARP10 (0.66) PARP10PARP15PARP4ALDH1A1KMT2A
SCHEMBL12516203 0.84 GAA (0.59) ALDH1A1KMT2AL3MBTL1GAA
SCHEMBL7957567 0.83 PARP10 (0.66) PARP10PARP15PARP4ALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2532651-B1 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1h)-yl]propoxy}benzamide hydrochloride and its free base as well as the pharmaceutical compositions containing them SERVIER LAB (FR) 2015-08-05 EP claimed
US-8952179-B2 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]propoxy} benzamide hydrochloride and pharmaceutical compositions containing it LES LABORATORIES SERVIER (FR) 2015-02-10 US claimed
US-20140100374-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4- BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT LES LABORATOIRES SERVIER (FR) 2014-04-10 US claimed
WO-2012168657-A1 PROCESS FOR SYNTHESIS AND CRYSTALLINE FORM OF 4-{3-[CIS-HEXAHYDROCYCLOPENTA[C]PYRROL-2(1H)-YL]PROPOXY}BENZAMIDE HYDROCHLORIDE, IN ADDITION TO THE ASSOCIATED FREE BASE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2012-12-13 WO claimed
US-20120316214-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4-BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT LES LABORATOIRES SERVIER (FR) 2012-12-13 US claimed
EP-2532651-A1 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1h)-yl]propoxy}benzamide hydrochloride and its free base as well as the pharmaceutical compositions containing them Les Laboratoires Servier (FR) 2012-12-12 EP claimed
EP-2532651-B1 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1h)-yl]propoxy}benzamide hydrochloride and its free base as well as the pharmaceutical compositions containing them SERVIER LAB (FR) 2015-08-05 EP disclosed
US-8952179-B2 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]propoxy} benzamide hydrochloride and pharmaceutical compositions containing it LES LABORATORIES SERVIER (FR) 2015-02-10 US disclosed
US-20140155453-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4-{3[CIS-HEXAHYDROCYCLOPENT A[CjPYRROL-2( 1 H)-YLjPROPOXYj BENZAMI DE HYDROCHLORI DE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT LES LABORATOIRES SERVIER (FR) 2014-06-05 US disclosed
US-20140100374-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4- BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT LES LABORATOIRES SERVIER (FR) 2014-04-10 US disclosed
US-8664408-B2 Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]proxy}benzamide hydrochloride and pharmaceutical compositions containing it LES LABORATOIRES SERVIER (FR) 2014-03-04 US disclosed
CN-102127004-B Azabicyclo[3.2.0]hept-3-yl, method for preparing same and pharmaceutical compositions containing them SERVIER LAB 2013-10-23 CN disclosed
EP-2332910-B1 New derivatives of azabicyclo[3.2.0]hept-3-yl, method for preparing same and pharmaceutical compositions containing them SERVIER LAB (FR) 2013-01-30 EP disclosed
EP-1866293-A1 COMPOUNDS COMPRISING AN OXAZOLE OR THIAZOLE MOIETY, PROCESSES FOR MAKING THEM, AND THEIR USES UCB Pharma, S.A. (BE) 2007-12-19 EP disclosed
WO-2006103045-A1 COMPOUNDS COMPRISING AN OXAZOLE OR THIAZOLE MOIETY, PROCESSES FOR MAKING THEM, AND THEIR USES UCB PHARMA S.A. (BE) 2006-10-05 WO disclosed
US-4950674-A Arylalkylheterocyclic amines,N-substituted by aryloxyalkyl group in a method for allergy treatment A. H. ROBINS COMPANY, INCORPORATED (US) 1990-08-21 US disclosed
US-4895840-A ANTIARRHYTHMIA AGENTS A. H. ROBINS COMPANY, INCORPORATED (US) 1990-01-23 US disclosed
US-4810713-A Arylalkyl-heterocyclic amines, n-substituted by aryloxyalkyl groups used in a method for allergy treatment A. H. ROBINS COMPANY, INCORPORATED (US) 1989-03-07 US disclosed
EP-0295010-A1 Derivatives of alkylaminoalkyl ureas and cyanoguanidines A.H. ROBINS COMPANY, INCORPORATED (US) 1988-12-14 EP disclosed
EP-0235463-A2 N-substituted-arylalkyl and arylalkylene piperidines as cardiovascular antihistaminic and antisecretory agents A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1987-09-09 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 (3 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-20140155453-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4-{3[CIS-HEXAHYDROCYCLOPENT A[CjPYRROL-2( 1 H)-YLjPROPOXYj BENZAMI DE HYDROCHLORI DE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT HRH2, HRH1, HRH4 PARP10 4568/4885PARP15 3819/4885PARP4 4144/4885
US-20120316214-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4-BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT HRH4, HRH2, HRH1 PARP10 3022/4885PARP15 1834/4885PARP4 1385/4885
US-20140100374-A1 SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4- BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT CYP4B1, CYP3A4, CYP4F8 PARP10 2733/4885PARP15 1116/4885PARP4 665/4885

“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.