Cilnidipine

Cilnidipine

SCHEMBL29367885

COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OC/C=C/c2ccccc2)C1c1cccc([N+](=O)[O-])c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1S

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CACNA1C known ✓ Q13936 8/20 1.00
CACNA1F known ✓ O60840 7/20 0.69
CACNA1D known ✓ Q01668 7/20 0.69
CACNA1S known ✓ Q13698 7/20 0.69
CACNA1B Q00975 5/20 1.00
MEN1 O00255 5/20 1.00
KMT2A Q03164 5/20 1.00
ADORA3 P0DMS8 2/20 1.00
MLNR O43193 1/20 1.00
NR1I2 O75469 1/20 1.00
CACNA1H O95180 1/20 1.00
NR3C1 P04150 1/20 1.00
TBXA2R P21731 1/20 1.00
HTT P42858 1/20 1.00
PDE4D Q08499 1/20 1.00
SLC29A1 Q99808 1/20 1.00
CYP1A2 P05177 4/20 0.71
CYP3A4 P08684 4/20 0.71
CYP2C9 P11712 4/20 0.71
CYP2C19 P33261 4/20 0.71

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
Cilnidipine SCHEMBL25550 1.00 CACNA1C (1.00) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL31398437 1.00 CACNA1C (1.00) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL25551 1.00 CACNA1C (1.00) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL30209784 1.00 CACNA1C (1.00) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL3334757 1.00 CACNA1C (1.00) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL28356318 0.99 CACNA1C (0.98) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL29248832 0.99 CACNA1C (0.98) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL27852253 0.97 CACNA1C (0.95) CACNA1CCACNA1BMEN1KMT2AADORA3
Cilnidipine SCHEMBL29141421 0.95 CACNA1C (0.90) CACNA1CCACNA1BMEN1KMT2AADORA3
SCHEMBL10739961 0.94 CACNA1B (0.94) CACNA1CCACNA1BMEN1KMT2AADORA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4741007-A2 METHOD OF TREATING OR PREVENTING AN ADVERSE SECONDARY NEUROLOGICAL OUTCOME FOLLOWING A HAEMORRHAGIC STROKE CSL Behring AG (CH) 2026-05-13 EP disclosed
EP-3558298-B1 ANTIDIABETIC SPIROCHROMAN COMPOUNDS MERCK SHARP & DOHME LLC (US) 2026-03-11 EP disclosed
US-20250346646-A1 COMPOUNDS USEFUL TO TREAT METABOLIC DISORDERS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2025-11-13 US disclosed
US-20250304655-A1 Expression System for Producing a Recombinant Haptoglobin (Hp) Beta Chain CSL BEHRING AG (CH) 2025-10-02 US disclosed
EP-2958562-B1 ANTIDIABETIC BICYCLIC COMPOUNDS MERCK SHARP & DOHME LLC (US) 2025-09-10 EP disclosed
US-20250171497-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LIMITED (IE) 2025-05-29 US disclosed
US-20250049881-A1 FORMULATIONS OF GUANYLATE CYCLSE C AGONISTS AND METHODS OF USE JPMORGAN CHASE BANK, N.A. 2025-02-13 US disclosed
US-20250026719-A1 NOVEL COMPOUNDS AS INHIBITORS OF PCSK9 SHENGKE PHARMACEUTICALS (JIANGSU) LTD. (CN) 2025-01-23 US disclosed
US-12146003-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2024-11-19 US disclosed
EP-4424697-A2 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME Bausch Health Ireland Limited (IE) 2024-09-04 EP disclosed
EP-4090650-A1 NOVEL COMPOUNDS AS INHIBITORS OF PCSK9 Shengke Pharmaceuticals (Jiangsu) Ltd. (CN) 2022-11-23 EP disclosed
WO-2022234070-A1 EXPRESSION SYSTEM FOR PRODUCING A RECOMBINANT HAPTOGLOBIN (HP) BETA CHAIN CSL BEHRING AG (CH) 2022-11-10 WO disclosed
CN-109642908-B Compounds useful for treating metabolic disorders 哈佛学院院长及董事 2022-08-16 CN disclosed
WO-2022162218-A1 METHOD OF TREATING OR PREVENTING AN ADVERSE SECONDARY NEUROLOGICAL OUTCOME FOLLOWING A HAEMORRHAGIC STROKE CSL BEHRING AG (CH) 2022-08-04 WO disclosed
US-20220211808-A1 HAPTOGLOBIN FOR USE IN TREATING AN ADVERSE SECONDARY NEUROLOGICAL OUTCOME FOLLOWING A HAEMORRHAGIC STROKE UNIVERSITAET ZUERICH (CH) 2022-07-07 US disclosed
US-11345748-B2 Method of treating idiopathic pulmonary fibrosis and kidney fibrosis PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2022-05-31 US disclosed
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2022-05-03 US disclosed
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LIMITED (IE) 2022-04-21 US disclosed
EP-3968988-A1 HAPTOGLOBIN FOR USE IN TREATING AN ADVERSE SECONDARY NEUROLOGICAL OUTCOME FOLLOWING A HAEMORRHAGIC STROKE Universität Zürich (CH) 2022-03-23 EP disclosed
CN-114007639-A Haptoglobin for the treatment of adverse secondary neurological consequences following hemorrhagic stroke 苏黎世大学 2022-02-01 CN 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 (6 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-12146003-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 CACNA1C 671/4885CACNA1F 1605/4885CACNA1D 1070/4885
US-20250171497-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 CACNA1C 671/4885CACNA1F 1605/4885CACNA1D 1070/4885
US-20250026719-A1 NOVEL COMPOUNDS AS INHIBITORS OF PCSK9 PCSK9, PCSK7, PCSK6 CACNA1C 4774/4885CACNA1F 4723/4885CACNA1D 4739/4885
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 CACNA1C 671/4885CACNA1F 1605/4885CACNA1D 1070/4885
US-11345748-B2 Method of treating idiopathic pulmonary fibrosis and kidney fibrosis CNR2, FABP1, FABP4 CACNA1C 2642/4885CACNA1F 2950/4885CACNA1D 2787/4885
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 CACNA1C 671/4885CACNA1F 1605/4885CACNA1D 1070/4885

“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.