SCHEMBL4397444

SCHEMBL4397444

CCC[C@H](N[C@H](C)C(=O)OCc1ccccc1)C(=O)OCC

nearest known ligand 0.51

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ACE P12821 9/20 0.51
LMNA P02545 3/20 0.49
CTSK P43235 1/20 0.49
ABCB11 O95342 2/20 0.47
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
USP2 O75604 1/20 0.46
CYP3A4 P08684 1/20 0.46
ALOX15 P16050 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.45
HSD17B10 Q99714 1/20 0.44

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
SCHEMBL4395799 1.00 ACE (0.51) ACELMNACTSKABCB11MEN1
SCHEMBL4395801 1.00 ACE (0.51) ACELMNACTSKABCB11MEN1
SCHEMBL9773242 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL7342910 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL7342915 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL9257644 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL9773173 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL10829372 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL9773168 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A
SCHEMBL7343890 0.92 ACE (0.57) ACELMNAABCB11MEN1KMT2A

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 6 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
US-20060276659-A1 Process for preparation of perindopril and salts thereof LIPIN LIMITED (IN) 2006-12-07 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 10/4885LMNA 806/4885CTSK 1362/4885
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 8/4885LMNA 1430/4885CTSK 3871/4885

“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.