Moexipril

Moexipril

SCHEMBL678818

CCOC(=O)C(CCc1ccccc1)NC(C)C(=O)N1Cc2cc(OC)c(OC)cc2CC1C(=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 Moexipril. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 15/20 1.00
PDE3A Q14432 1/20 1.00
ABCB11 O95342 2/20 0.80
LMNA P02545 1/20 0.64
SMN1; SMN2 Q16637 1/20 0.59
AGTR2 P50052 1/20 0.56

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
Moexipril SCHEMBL6508276 1.00 ACE (1.00) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL29376544 1.00 ACE (1.00) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL683321 1.00 ACE (1.00) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL22175779 1.00 ACE (1.00) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL34030 1.00 ACE (1.00) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL5159178 0.99 ACE (0.98) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL40877 0.99 ACE (0.98) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL14660386 0.99 ACE (0.98) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL30903896 0.99 ACE (0.98) ACEPDE3AABCB11LMNASMN1; SMN2
Moexipril SCHEMBL5386742 0.99 ACE (0.98) ACEPDE3AABCB11LMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0096157-A2 Substituted acyl derivatives of 1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid WARNER-LAMBERT COMPANY (US) 1983-12-21 EP claimed
US-4344949-A Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids WARNER-LAMBERT COMPANY (US) 1982-08-17 US claimed
EP-0049605-A1 Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids, salts thereof, pharmaceutical compositions containing the derivatives or salts, and the production of the same WARNER-LAMBERT COMPANY (US) 1982-04-14 EP claimed
US-8394813-B2 Active agent delivery systems and methods for protecting and administering active agents SHIRE LLC (US) 2013-03-12 US disclosed
WO-2012054438-A1 ANTI-PCSK9 SCHERING CORPORATION (US) 2012-04-26 WO disclosed
US-20110269717-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN BRAINCELLS INC. (US) 2011-11-03 US disclosed
EP-2382975-A2 Neurogenesis by modulating angiotensin Braincells, Inc. (US) 2011-11-02 EP disclosed
EP-2377531-A2 Neurogenesis by modulating angiotensin Braincells, Inc. (US) 2011-10-19 EP disclosed
US-20110092464-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN BRAINCELLS INC. (US) 2011-04-21 US disclosed
US-20110046090-A1 MODULATION OF NEUROGENESIS WITH GABA AGENTS AND GABA ANALOGS BRAINCELLS INC. (US) 2011-02-24 US disclosed
US-7858611-B2 Neurogenesis by modulating angiotensin BRAINCELLS INC. (US) 2010-12-28 US disclosed
US-7427600-B2 Active agent delivery systems and methods for protecting and administering active agents SHIRE LLC (US) 2008-09-23 US disclosed
US-20080167291-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN BRAINCELLS, INC. (US) 2008-07-10 US disclosed
WO-2007134136-A2 NEUROGENESIS BY MODULATING ANGIOTENSIN BRAINCELLS, INC. (US) 2007-11-22 WO disclosed
US-20070232529-A1 mesalamine covalently attached to carrier peptide at C-terminus, interspersed and/or side chain; releasing into bloodstream; reducing dosage NEW RIVER PHARMACEUTICALS INC. (US) 2007-10-04 US disclosed
EP-0049605-B1 SUBSTITUTED ACYL DERIVATIVES OF 1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACIDS, SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS CONTAINING THE DERIVATIVES OR SALTS, AND THE PRODUCTION OF THE SAME WARNER-LAMBERT COMPANY (US) 1987-03-18 EP disclosed
US-4532342-A N-substituted amino acids as intermediates in the preparation of acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids WARNER-LAMBERT COMPANY (US) 1985-07-30 US disclosed
EP-0096157-A2 Substituted acyl derivatives of 1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid WARNER-LAMBERT COMPANY (US) 1983-12-21 EP disclosed
US-4344949-A Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids WARNER-LAMBERT COMPANY (US) 1982-08-17 US disclosed
EP-0049605-A1 Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids, salts thereof, pharmaceutical compositions containing the derivatives or salts, and the production of the same WARNER-LAMBERT COMPANY (US) 1982-04-14 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 (5 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-20110046090-A1 MODULATION OF NEUROGENESIS WITH GABA AGENTS AND GABA ANALOGS GAP43, GABRB1, GABRB3 ACE 4514/4885PDE3A 203/4885ABCB11 4659/4885
US-20110092464-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN DCX, NGF, BDNF ACE 10/4885PDE3A 478/4885ABCB11 4712/4885
US-20110269717-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN NGF, DCX, BDNF ACE 6/4885PDE3A 413/4885ABCB11 4566/4885
US-20070232529-A1 mesalamine covalently attached to carrier peptide at C-terminus, interspersed and/or side chain; releasing into bloodstream; reducing dosage VIP, BST2, FCGR3B ACE 948/4885PDE3A 821/4885ABCB11 307/4885
US-20080167291-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN DCX, NGF, BDNF ACE 10/4885PDE3A 488/4885ABCB11 4712/4885

“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.