Lisinopril Anhydrous

Lisinopril Anhydrous

SCHEMBL454824

NCCCC[C@H](N[C@@H](CCc1ccccc1)C(=O)O)C(=O)N1CCC[C@H]1C(=O)O.O

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACE

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 8/20 0.98
LMNA P02545 1/20 0.57
SMN1; SMN2 Q16637 1/20 0.53
F2 P00734 1/20 0.50

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
Lisinopril Anhydrous SCHEMBL29047795 1.00 ACE (0.98) ACELMNASMN1; SMN2F2
Lisinopril Anhydrous SCHEMBL677321 1.00 ACE (0.98) ACELMNASMN1; SMN2F2
Lisinopril Anhydrous SCHEMBL1268274 1.00 ACE (0.98) ACELMNASMN1; SMN2F2
Lisinopril Anhydrous SCHEMBL31692087 1.00 ACE (0.98) ACELMNASMN1; SMN2F2
Lisinopril Anhydrous SCHEMBL542591 1.00 ACE (0.98) ACELMNASMN1; SMN2F2
Lisinopril Anhydrous SCHEMBL24062681 0.99 ACE (1.00) ACELMNASMN1; SMN2
Lisinopril Anhydrous SCHEMBL15680 0.99 ACE (1.00) ACELMNASMN1; SMN2
Lisinopril Anhydrous SCHEMBL156900 0.99 ACE (1.00) ACELMNASMN1; SMN2
Lisinopril Anhydrous SCHEMBL7268245 0.99 ACE (1.00) ACELMNASMN1; SMN2
Lisinopril Anhydrous SCHEMBL18712916 0.99 ACE (1.00) 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 140 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2003022872-A2 CRYSTAL FORM OF LISINOPRIL MONOHYDRATE ASTRAZENECA AB (SE) 2003-03-20 WO claimed
US-6468976-B1 Monohydrate lisinopril ASTRAZENECA AB (SE) 2002-10-22 US claimed
US-6465615-B1 DISSOLVING (LISINOPRIL) 1-(N2 -((S)-1-CARBOXY-3-PHENYLPROPYL)-L-LYSYL)-L-PROLINE IN WATER, ADDING ISOBUTANOL TO THE SOLUTION TO INDUCE CRYSTALLIZATION OF LISINOPRIL, ISOLATING AND DRYING THE CRYSTALS ASTRAZENECA AB (SE) 2002-10-15 US claimed
CN-110831576-B Lisinopril compositions with ingestible event markers 大冢制药株式会社 2024-07-16 CN disclosed
CN-117946209-A Tumor targeting molecular probe and preparation method and application thereof 江西中医药大学 2024-04-30 CN disclosed
EP-4346811-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE University of Maryland, Baltimore (US) 2024-04-10 EP disclosed
US-11911480-B2 Self-emulsifying composition of ω-3 fatty acid MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2024-02-27 US disclosed
US-20230405079-A1 LISINOPRIL FORMULATIONS HPS INVESTMENT PARTNERS, LLC, AS ADMINISTRATIVE AGENT 2023-12-21 US disclosed
US-11771733-B2 Lisinopril formulations Silvergate Pharmaceuticals, Inc. (US) 2023-10-03 US disclosed
EP-3735963-B1 SELF-EMULSIFYING COMPOSITION OF OMEGA-3 FATTY ACID MOCHIDA PHARM CO LTD (JP) 2023-09-13 EP disclosed
US-11684605-B2 Lisinopril compositions with an ingestible event marker OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2023-06-27 US disclosed
WO-2003022872-A2 CRYSTAL FORM OF LISINOPRIL MONOHYDRATE ASTRAZENECA AB (SE) 2003-03-20 WO disclosed
WO-2003022872-A2 CRYSTAL FORM OF LISINOPRIL MONOHYDRATE ASTRAZENECA AB (SE) 2003-03-20 WO disclosed
WO-2003000716-A2 PREPARATION AND USE OF AMORPHOUS LISINOPRIL ASTRAZENECA AB (SE) 2003-01-03 WO disclosed
US-6468976-B1 Monohydrate lisinopril ASTRAZENECA AB (SE) 2002-10-22 US disclosed
US-6468976-B1 Monohydrate lisinopril ASTRAZENECA AB (SE) 2002-10-22 US disclosed
US-6465615-B1 DISSOLVING (LISINOPRIL) 1-(N2 -((S)-1-CARBOXY-3-PHENYLPROPYL)-L-LYSYL)-L-PROLINE IN WATER, ADDING ISOBUTANOL TO THE SOLUTION TO INDUCE CRYSTALLIZATION OF LISINOPRIL, ISOLATING AND DRYING THE CRYSTALS ASTRAZENECA AB (SE) 2002-10-15 US disclosed
US-6465615-B1 DISSOLVING (LISINOPRIL) 1-(N2 -((S)-1-CARBOXY-3-PHENYLPROPYL)-L-LYSYL)-L-PROLINE IN WATER, ADDING ISOBUTANOL TO THE SOLUTION TO INDUCE CRYSTALLIZATION OF LISINOPRIL, ISOLATING AND DRYING THE CRYSTALS ASTRAZENECA AB (SE) 2002-10-15 US disclosed
US-6462174-B1 ADMINISTERING LISINOPRIL AS HYPOTENSIVE AGENT; FAST MELTING ASTRAZENECA AB (SE) 2002-10-08 US disclosed
US-6458769-B1 AMORPHOUS LISINOPRIL HAVING THE FORMULA (S)-1-(N.SUP.2 -(1-CARBOXY-3-PHENYLPROPYL))-L-LYSYL)-L-PROLINE, WHEREIN AMORPHOUS LISINOPRIL HAS A GLASS TRANSITION POINT (TG) WHEN DRY, MEASURED BY THERMAL MEHANICAL ANALYSIS ASTRAZENECA AB (SE) 2002-10-01 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-11771733-B2 Lisinopril formulations REN, ACE, AGT ACE 2/4885LMNA 174/4885SMN1; SMN2 1363/4885
US-20230405079-A1 LISINOPRIL FORMULATIONS REN, ACE, AGT ACE 2/4885LMNA 174/4885SMN1; SMN2 1363/4885

“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.