Nilvadipine

drug
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Also known as CL 287,389CL-287,389CL-287389Dl-nilvadipineEscorFK 235FK-235FR-34235NilvadipinoNivadilNivadipNivadipineSK&F 102,362SK&F-102,362SK&F-102362SKF-102362SID50112689SID144205992NILVADIPINE (ARC029)

Summary

Nilvadipine (CHEMBL517427) is a phase-3 clinical-stage small molecule (ATC C08CA10); indicated across 2 conditions including cardiovascular disorder and alzheimer disease.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: C08CA10
  • Indications: 2 conditions
  • Clinical trials: 1
  • Chemistry: 385.4 Da · C19H19N3O6

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL517427
NameNilvadipine
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID4494
ATCC08CA10
Molecular formulaC19H19N3O6
Molecular weight385.4
InChIKeyFAIIFDPAEUKBEP-UHFFFAOYSA-N

SMILES: CC1=C(C(C(=C(N1)C#N)C(=O)OC)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OC(C)C

IUPAC name: 3-O-methyl 5-O-propan-2-yl 2-cyano-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

Also known as: CL 287,389, CL-287,389, CL-287389, Dl-nilvadipine, Escor, FK 235, FK-235, FR-34235, Nilvadipine, Nilvadipino, Nivadil, Nivadip

Patent coverage: 3,834 distinct patent families (14,439 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 14,435 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 14 (assay-derived). Sample: Sodium channel protein type 5 subunit alpha, Equilibrative nucleoside transporter 1, Glucocorticoid receptor, Thromboxane A2 receptor, Voltage-gated L-type calcium channel, Nuclear receptor subfamily 1 group I member 2, Type-1 angiotensin II receptor, Prostaglandin G/H synthase 2, Adenosine receptor A3, 3’,5’-cyclic-AMP phosphodiesterase 4D.

Bioactivity

ChEMBL activities: 12 potent at pChembl ≥ 5 of 19 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
P220028.98IC501.04nMCHEMBL_ACT_423556
P220027.97AC5010.7nMCHEMBL_ACT_25119644
SCN5A6.36AC50440nMCHEMBL_ACT_25158933
NR1I26.09AC50814.3nMCHEMBL_ACT_25188221
NR1I26.05EC50890nMCHEMBL_ACT_15465496
NR1I26AC501006nMCHEMBL_ACT_25224373
NR1I25.85EC501400nMCHEMBL_ACT_15448137
NR1I25.72EC501900nMCHEMBL_ACT_15463802
NR1I25.7EC502000nMCHEMBL_ACT_15463756
SLC29A15.45AC503590nMCHEMBL_ACT_25141603
NR3C15.3AC505000nMCHEMBL_ACT_25175907
PDE4D5.09AC508060nMCHEMBL_ACT_25185395

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
cardiovascular disorder3MONDO:0004995EFO:0000319
Alzheimer disease3MONDO:0004975MONDO:0004975

Clinical trials

Total trials: 1.

Phase distribution

PhaseTrials
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02017340PHASE3COMPLETEDA Phase III Trial of Nilvadipine to Treat Alzheimer’s Disease

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).