Enalapril

Enalapril

SCHEMBL1650291

CCOC(=O)[C@@H](CCc1ccccc1)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)O.O=C(O)/C=C\C(=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 Enalapril. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 14/20 0.91
SMN1; SMN2 Q16637 1/20 1.00
LMNA P02545 2/20 0.91
ABCB11 O95342 2/20 0.65
MEN1 O00255 2/20 0.63
KMT2A Q03164 2/20 0.63
USP2 O75604 1/20 0.63
CYP3A4 P08684 1/20 0.63
ALOX15 P16050 1/20 0.63
PDE3A Q14432 1/20 0.59

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
Enalapril SCHEMBL20817249 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL10 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL2719411 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL6155137 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL10390115 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL308603 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL825430 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9019924 0.99 SMN1; SMN2 (0.98) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9019927 0.99 SMN1; SMN2 (0.98) SMN1; SMN2ACELMNAABCB11MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-121575079-A SGLT1/2 double-target inhibitor, screening method and application thereof, and diabetes treatment drug 广东药科大学 2026-02-27 CN claimed
CN-121575079-A SGLT1/2 double-target inhibitor, screening method and application thereof, and diabetes treatment drug 广东药科大学 2026-02-27 CN disclosed
CN-119970919-A Traditional Chinese medicine composition and traditional Chinese medicine preparation for treating hypertension and heart failure and application of traditional Chinese medicine composition and traditional Chinese medicine preparation 中国中医科学院广安门医院 2025-05-13 CN disclosed
US-20210393645-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2021-12-23 US disclosed
CN-107951835-B Enalapril maleate preparation and application thereof 湖南千金湘江药业股份有限公司 2021-08-24 CN disclosed
CN-112225778-A Preparation method of enalapril maleate 辰欣药业股份有限公司 2021-01-15 CN disclosed
US-20200338114-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS OR INFLAMMATORY DISEASE USING LOW SULPHATE FUCANS ARC MEDICAL DEVICES INC. (CA) 2020-10-29 US disclosed
US-20190262353-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2019-08-29 US disclosed
CN-109734775-A A kind of refining methd of enalapril maleate 辰欣药业股份有限公司 2019-05-10 CN disclosed
CN-107951835-A A kind of enalapril maleate preparation and its application 湖南千金湘江药业股份有限公司 2018-04-24 CN disclosed
US-20100222311-A1 SOLID FORMULATIONS OF CRYSTALLINE COMPOUNDS PURDUE RESEARCH FOUNDATION (US) 2010-09-02 US disclosed
EP-1809303-A4 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS OR INFLAMMATORY DISEASE USING LOW SULPHATE FUCANS ARC PHARMACEUTICALS INC (CA) 2008-12-24 EP disclosed
US-20080063682-A1 Pharmaceutical compositions and methods relating to inhibiting fibrous adhesions or inflammatory disease using low sulphate fucans ARC MEDICAL DEVICES, INC. (CA) 2008-03-13 US disclosed
EP-1809303-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS OR INFLAMMATORY DISEASE USING LOW SULPHATE FUCANS ARC PHARMACEUTICALS, INC. (CA) 2007-07-25 EP disclosed
WO-2006032143-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS OR INFLAMMATORY DISEASE USING LOW SULPHATE FUCANS ARC PHARMACEUTICALS, INC. (CA) 2006-03-30 WO disclosed
WO-2006032144-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS OR INFLAMMATORY DISEASE USING FUCANS FROM VARIOUS ECHINODERM SOURCES ARC PHARMACEUTICALS, INC. (CA) 2006-03-30 WO disclosed
EP-1631265-A2 USE OF VARIOUS AGENTS FOR INHIBITING FIBROUS ADHESIONS ARC PHARMACEUTICALS, INC. (CA) 2006-03-08 EP disclosed
WO-2004105737-A2 PHARMACEUTICAL COMPOSITIONS AND METHODS RELATING TO INHIBITING FIBROUS ADHESIONS USING VARIOUS AGENTS ARC PHARMACEUTICALS, INC. (CA) 2004-12-09 WO disclosed
US-6204393-B1 IN AQUEOUS SOLUTION; CONTROLLING PH; NEUTRALIZATION KANEKA CORPORATION (JP) 2001-03-20 US disclosed
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 disclosed