Felodipine

Felodipine

SCHEMBL26398

CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1cccc(Cl)c1Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1SNR3C2

The experimentally established mechanism targets of Felodipine. 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 2/20 0.61
CACNA1F known ✓ O60840 1/20 0.58
CACNA1D known ✓ Q01668 1/20 0.58
CACNA1S known ✓ Q13698 1/20 0.58
CYP2C9 P11712 5/20 1.00
CYP3A4 P08684 5/20 1.00
HIF1A Q16665 5/20 1.00
KDM4E B2RXH2 4/20 1.00
MEN1 O00255 4/20 1.00
CYP1A2 P05177 4/20 1.00
CYP2C19 P33261 4/20 1.00
KMT2A Q03164 4/20 1.00
MAPT P10636 4/20 1.00
ABCB11 O95342 3/20 1.00
ADORA3 P0DMS8 3/20 1.00
TBXA2R P21731 3/20 1.00
ADRA1A P35348 3/20 1.00
SLC6A3 Q01959 3/20 1.00
TSHR P16473 3/20 1.00
HSD17B10 Q99714 2/20 1.00

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
(R)-Felodipine SCHEMBL29617765 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL13460298 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL920025 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
(S)-Felodipine SCHEMBL26399 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
(R)-Felodipine SCHEMBL54486 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
(S)-Felodipine SCHEMBL29908048 1.00 CYP2C9 (1.00) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL29049073 0.99 CYP2C9 (0.98) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL27770064 0.99 CYP2C9 (0.98) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL27608150 0.99 CYP2C9 (0.98) CYP2C9CYP3A4HIF1AKDM4EMEN1
Felodipine SCHEMBL28260282 0.98 CYP2C9 (0.95) CYP2C9CYP3A4HIF1AKDM4EMEN1

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

Appears in 33935 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3607938-B1 PHARMACEUTICAL COMPOSITION SOVIC BRKICIC LJILJANA (HR) 2026-05-27 EP claimed
WO-2026107071-A1 COMBINATION THERAPY Retension Pharmaceuticals, Inc. (US) 2026-05-21 WO claimed
WO-2026107412-A1 SARCOSPAN MODULATION AND METHODS OF MEAT AND TISSUE CULTURE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2026-05-21 WO claimed
EP-4741492-A2 NECROSIS INHIBITOR Linkgevity Limited (GB) 2026-05-13 EP claimed
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 EP claimed
WO-2026087680-A1 TREATMENT FOR CARDIOVASCULAR DISEASE SAPREME TECHNOLOGIES B.V. (NL) 2026-04-30 WO claimed
US-20260115145-A1 Method for Enhancing Drug Solubility and Preparing a Drug Composite Material with Enhanced Solubility PHARMAEASE TECH LTD (CN) 2026-04-30 US claimed
EP-3934654-B1 ISTAROXIME OR ITS METABOLITE PST-3093 FOR USE AS INTRAVENOUS FORMULATION FOR THE TREATMENT OF ACUTE HEART FAILURE (AHF) WINDTREE THERAPEUTICS INC (US) 2026-04-29 EP claimed
US-12605345-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2026-04-21 US claimed
EP-4724060-A1 FORMULATIONS AND METHODS FOR TREATING NEUROPSYCHIATRIC DISORDERS HB Biotech, Inc. (US) 2026-04-15 EP claimed
WO-1986003676-A1 SMALL PARTICLE FORMATION AND ENCAPSULATION THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1986-07-03 WO claimed
US-4584294-A Fused tricyclic lactams as angiotensin converting enzyme inhibitors and as antihypertensive agents MERCK & CO., INC. (US) 1986-04-22 US claimed
EP-0166353-A2 Benzofused lactams useful as antihypertensive agents and as cholecystokinin antagonists MERCK & CO. INC. (US) 1986-01-02 EP claimed
EP-0163237-A2 Di- and tri-peptidal renin inhibitors MERCK & CO. INC. (US) 1985-12-04 EP claimed
WO-1985000110-A1 SMALL PARTICLE FORMATION OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1985-01-17 WO claimed
EP-0130160-A2 Small particle formation THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1985-01-02 EP claimed
EP-0129189-A2 Renin inhibitors containing a C-terminal amide cycle and compositions and combinations containing the same MERCK & CO. INC. (US) 1984-12-27 EP claimed
EP-0095450-A2 Processes for preparing therapeutically active dihydropyridines and intermediates for the processes Aktiebolaget Hässle (SE) 1983-11-30 EP claimed
EP-0007293-B1 2,6-DIMETHYL-4-(2,3-DICHLOROPHENYL)-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLIC ACID-3-METHYL ESTER-5-ETHYL ESTER HAVING HYPOTENSIVE PROPERTIES, PROCESS FOR ITS PREPARATION AND PHARMACEUTICAL PREPARATIONS CONTAINING IT Aktiebolaget Hässle (SE) 1982-06-23 EP claimed
US-4264611-A HYPOTENSIVE AGENTS AKTIEBOLAGET HASSLE (SE) 1981-04-28 US claimed