Imidapril

Imidapril

SCHEMBL3193644

CCOC(=O)C(CCc1ccccc1)N[C@@H](C)C(=O)N1C(=O)N(C)C[C@H]1C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACE

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 13/20 1.00
LMNA P02545 2/20 0.66
ABCB11 O95342 2/20 0.64
MEN1 O00255 2/20 0.61
KMT2A Q03164 2/20 0.61
USP2 O75604 1/20 0.61
CYP3A4 P08684 1/20 0.61
ALOX15 P16050 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61

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
Imidapril SCHEMBL22492310 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL6516062 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL683273 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL7354516 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL11014327 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL34098 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL34099 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL12894585 1.00 ACE (1.00) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL7294155 0.99 ACE (0.98) ACELMNAABCB11MEN1KMT2A
Imidapril SCHEMBL136722 0.99 ACE (0.98) 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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100029734-A1 METHODS FOR BREAST CANCER SCREENING AND TREATMENT ORE PHARMACEUTICALS INC. (US) 2010-02-04 US disclosed
US-6610682-B2 Comprising insulin resistance improving agents in combination with drugs selected from angiotensin II receptor antagonists and angiotensin converting enzyme inhibitors with a diluent or carrier SANKYO COMPANY, LIMITED (JP) 2003-08-26 US disclosed
US-20020013308-A1 Comprising insulin resistance improving agents in combination with drugs selected from angiotensin II receptor antagonists and angiotensin converting enzyme inhibitors with a diluent or carrier SANKYO COMPANY LIMITED (JP) 2002-01-31 US disclosed
EP-1175902-A1 Use of CS-866 (olmesartan) in the manufacture of a medicament for treating arteriosclerosis Sankyo Company Limited (JP) 2002-01-30 EP disclosed
EP-0930076-A1 MEDICINAL COMPOSITIONS SANKYO COMPANY LIMITED (JP) 1999-07-21 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 (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-20020013308-A1 Comprising insulin resistance improving agents in combination with drugs selected from angiotensin II receptor antagonists and angiotensin converting enzyme inhibitors with a diluent or carrier AGTR1, AGTR2, ACE ACE 3/4885LMNA 543/4885ABCB11 397/4885

“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.