Enalaprilat Anhydrous

Enalaprilat Anhydrous

SCHEMBL3090322

C[C@H](NC(CCc1ccccc1)C(=O)O)C(=O)N1CCC[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 Enalaprilat Anhydrous. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 13/20 1.00
LMNA P02545 1/20 0.81
SMN1; SMN2 Q16637 1/20 0.74

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
Enalaprilat Anhydrous SCHEMBL12737170 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL18033873 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL2406720 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL37289 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL11204535 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL24327564 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL6106603 1.00 ACE (1.00) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL8149345 0.99 ACE (0.98) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL21046169 0.99 ACE (0.98) ACELMNASMN1; SMN2
Enalaprilat Anhydrous SCHEMBL37288 0.99 ACE (0.98) ACELMNASMN1; 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 71 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060104913-A1 Inhalable formulations for treating pulmonary hypertension and methods of using same MERCK PATENT GMBH 2006-05-18 US claimed
US-20040265238-A1 Inhalable formulations for treating pulmonary hypertension and methods of using same DEY PHARMA, L.P. (F/K/A DEY L.P.) 2004-12-30 US claimed
US-20030105327-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid KANEKA CORPORATION (JP) 2003-06-05 US claimed
US-6518436-B2 Condensing an amino acid and N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanine-N-carboxy-anhydride; suppressing the by-product diketopiperazine derivative; making enalapril maleate KANEKA CORPORATION (JP) 2003-02-11 US claimed
US-20020087007-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid KANEKA CORPORATION (JP) 2002-07-04 US claimed
US-6204393-B1 IN AQUEOUS SOLUTION; CONTROLLING PH; NEUTRALIZATION KANEKA CORPORATION (JP) 2001-03-20 US claimed
EP-1018516-A1 METHOD FOR CRYSTALLIZING MALEIC ACID SALT OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL-L-PROLINE KANEKA CORPORATION (JP) 2000-07-12 EP claimed
EP-0967221-A1 PROCESS FOR PREPARING PHARMACOLOGICALLY ACCEPTABLE SALTS OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL AMINO ACIDS KANEKA CORPORATION (JP) 1999-12-29 EP claimed
US-5238924-A Treatment of renal diseases with ace inhibitors MERCK & CO., INC. (US) 1993-08-24 US claimed
EP-0463636-A2 Cardiovascular composition MERCK FROSST CANADA INC. (CA) 1992-01-02 EP claimed
EP-0129136-B1 ANTIHYPERTENSIVE COMPOSITION MERCK & CO. INC. (US) 1991-10-30 EP claimed
US-4663307-A Anti-allergic and anti-thromboembolic 6H-dibenz-[b,e][1,4]-oxathiepin derivatives, compositions, and method of use therefor MERCK FROSST CANADA, INC. (CA) 1987-05-05 US claimed
EP-0166257-A2 Cardiovascular composition MERCK FROSST CANADA INC. (CA) 1986-01-02 EP claimed
EP-0129136-A2 Antihypertensive composition MERCK & CO. INC. (US) 1984-12-27 EP claimed
US-4472384-A INTERPHENYLENE 9-THIA-11-OXO-12-AZA PROSTANOIC ACID DERIVATIVE AND CARBOXYALKYLDIPEPTIDE MERCK & CO., INC. (US) 1984-09-18 US claimed
EP-0079521-A1 Process for preparation of carboxyalkyldipeptide derivatives MERCK & CO. INC. (US) 1983-05-25 EP claimed
US-4374829-A Aminoacid derivatives as antihypertensives MERCK & CO., INC. (US) 1983-02-22 US claimed
EP-0012401-A1 Carboxyalkyl dipeptide derivatives, process for preparing them and pharmaceutical composition containing them MERCK & CO. INC. (US) 1980-06-25 EP claimed
JP-2131496-A None JP disclosed
EP-0012401-A1 Carboxyalkyl dipeptide derivatives, process for preparing them and pharmaceutical composition containing them MERCK & CO. INC. (US) 1980-06-25 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 (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-20030105327-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid SLC7A1, ASS1, ALDH7A1 ACE 67/4885LMNA 765/4885SMN1; SMN2 496/4885
US-20020087007-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid SLC7A1, ASS1, ALDH7A1 ACE 67/4885LMNA 765/4885SMN1; SMN2 496/4885

“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.