SCHEMBL4404273

SCHEMBL4404273

CCOC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@H](C)NC(=O)OC(C)(C)C

nearest known ligand 0.53

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ACE P12821 7/20 0.53
KMT2A Q03164 4/20 0.48
MEN1 O00255 3/20 0.48
USP2 O75604 1/20 0.48
LMNA P02545 1/20 0.48
CTSL P07711 2/20 0.47
CYP3A4 P08684 1/20 0.46
ALOX15 P16050 1/20 0.46
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
ELANE P08246 1/20 0.37
HRH2 P25021 1/20 0.36
HRH1 P35367 1/20 0.36
FKBP1A P62942 2/20 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
SCHEMBL9775205 0.86 ACE (0.44) ACEKMT2AMEN1USP2LMNA
SCHEMBL10747717 0.85 ACE (0.55) ACEKMT2AMEN1USP2LMNA
SCHEMBL5364563 0.85 ACE (0.55) ACEKMT2AMEN1USP2LMNA
SCHEMBL5716228 0.85 ACE (0.55) ACEKMT2AMEN1USP2LMNA
SCHEMBL5716232 0.85 ACE (0.55) ACEKMT2AMEN1USP2LMNA
SCHEMBL9256682 0.85 CTSL (0.54) ACEKMT2AMEN1USP2LMNA
SCHEMBL9592654 0.83 CTSL (0.54) ACEKMT2AMEN1USP2LMNA
SCHEMBL9773233 0.83 CTSL (0.54) ACEKMT2AMEN1USP2LMNA
SCHEMBL9775310 0.83 ACE (0.53) ACEKMT2AMEN1USP2LMNA
SCHEMBL9175234 0.82 ACE (0.60) ACEKMT2AMEN1USP2LMNA

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1675827-B1 NOVEL METHOD FOR PREPARATION OF CRYSTALLINE PERINDOPRIL ERBUMINE SERVIER LAB (FR) 2009-12-16 EP disclosed
US-7521566-B2 Process for preparation of perindopril and salts thereof LES LABORATOIRES SERVIER (FR) 2009-04-21 US disclosed
US-7456296-B2 Method for preparation of crystalline perindopril erbumine LUPIN LTD (IN) 2008-11-25 US disclosed
EP-1603558-B1 PROCESS FOR PREPARATION OF PERINDOPRIL AND SALTS THEREOF SERVIER S A LAB (FR) 2008-05-21 EP disclosed
US-20070149604-A1 Reacting perindopril in a solvent selected from N,N-dimethylformamide, dimethoxymethane, 2,2-dimethoxypropane and 1,2-dimethoxyethane with tert-butylamine, crystallization; stereospecific LUPIN LTD. (IN) 2007-06-28 US disclosed
WO-2006137082-A1 PROCESS FOR INDUSTRIALLY VIABLE PREPARATION OF PERINDOPRIL ERBUMINE POTLURI RAMESH BABU (IN) 2006-12-28 WO disclosed
US-20060276659-A1 Process for preparation of perindopril and salts thereof LIPIN LIMITED (IN) 2006-12-07 US disclosed
EP-1675827-A1 NOVEL METHOD FOR PREPARATION OF CRYSTALLINE PERINDOPRIL ERBUMINE Lupin Limited (IN) 2006-07-05 EP disclosed
WO-2005037788-A1 NOVEL METHOD FOR PREPARATION OF CRYSTALLINE PERINDOPRIL ERBUMINE LUPIN LTD. (IN) 2005-04-28 WO disclosed
US-4644008-A Perhydroindole-2-carboxylic acids as antihypertensives ADIR (FR) 1987-02-17 US disclosed
US-4616031-A Perhydroindole-2-carboxylic acids as antihypertensives ADIR (FR) 1986-10-07 US disclosed
US-4616030-A Perhydroindole-2-carboxylic acids as antihypertensives ADIR (FR) 1986-10-07 US disclosed
US-4616029-A Perhydromdole-2-carboxylic acids as antihypertensives ADIR (FR) 1986-10-07 US disclosed
US-4565819-A ENZYME INHIBITORS, HYPOTENSIVE AGENTS ADIR (FR) 1986-01-21 US disclosed
US-4508729-A Substituted iminodiacids, their preparation and pharmaceutical compositions containing them ADIR (FR) 1985-04-02 US 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 (2 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-20060276659-A1 Process for preparation of perindopril and salts thereof CYP2C9, DPYD, CYP2C8 ACE 10/4885KMT2A 2501/4885MEN1 4541/4885
US-20070149604-A1 Reacting perindopril in a solvent selected from N,N-dimethylformamide, dimethoxymethane, 2,2-dimethoxypropane and 1,2-dimethoxyethane with tert-butylamine, crystallization; stereospecific REN, AGTR2, AGTR1 ACE 8/4885KMT2A 960/4885MEN1 4011/4885

“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.