General Information of Drug (ID: DM8NMAV)

Drug Name
1-[5-(4-Chlorophenyl)-2-furoyl]piperazine Drug Info
Synonyms CHEMBL521211; 1-[5-(4-Chlorophenyl)-2-furoyl]piperazine; BDBM50270649
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
24857857
TTD Drug ID
DM8NMAV

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Mephenytoin DM5UGDK Epilepsy 8A60-8A68 Approved [2]
Mexiletine DMCTE9R Ventricular tachycardia BC71 Approved [3]
Fosphenytoin DMOX3LB Epilepsy 8A60-8A68 Approved [2]
Disopyramide DM5SYZP Long QT syndrome BC65.0 Approved [3]
LOMERIZINE DME0TC8 Migraine 8A80 Approved [4]
Tetrodotoxin DMWMPRG Bacterial infection 1A00-1C4Z Approved [5]
Dyclonine DMU6OFP Pain MG30-MG3Z Approved [6]
Moricizine DMOMBJW Arrhythmia BC9Z Approved [7]
Ethotoin DMXWOCP Complex partial seizure 8A68.0 Approved [8]
Prilocaine DMI7DZ2 Pain MG30-MG3Z Approved [6]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Rilpivirine DMJ0QOW Human immunodeficiency virus infection 1C62 Approved [9]
Ropivacaine DMSPJG2 Anaesthesia 9A78.6 Approved [10]
Bupivacaine DM4PRFC Anaesthesia 9A78.6 Approved [10]
Tiapride DMN6CAG Alcohol dependence 6C40.2 Approved [11]
Tetracaine DM9J6C2 Spinal anesthesia MB40.3 Approved [12]
Proparacaine DMLS39E Anaesthesia 9A78.6 Approved [10]
Conatumumab DM2UOSN Colorectal cancer 2B91.Z Phase 2 [13]
VX-150 DMGDB21 Neuropathic pain 8E43.0 Phase 2 [14]
DSP-2230 DM0WTMD Neuropathic pain 8E43.0 Phase 1 [15]
PF-01247324 DM93LMS Pain MG30-MG3Z Phase 1 [16]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Voltage-gated sodium channel alpha Nav1.5 (SCN5A) TTZOVE0 SCN5A_HUMAN Inhibitor [1]
Voltage-gated sodium channel alpha Nav1.8 (SCN10A) TT90XZ8 SCNAA_HUMAN Inhibitor [1]

References

1 Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic pain. Bioorg Med Chem. 2008 Jun 15;16(12):6379-86.
2 Lacosamide: a new approach to target voltage-gated sodium currents in epileptic disorders. CNS Drugs. 2009;23(7):555-68.
3 Effect of sodium channel blockers on ST segment, QRS duration, and corrected QT interval in patients with Brugada syndrome. J Cardiovasc Electrophysiol. 2000 Dec;11(12):1320-9.
4 Medicinal chemistry of neuronal voltage-gated sodium channel blockers. J Med Chem. 2001 Jan 18;44(2):115-37.
5 Halothane attenuates the cerebroprotective action of several Na+ and Ca2+ channel blockers via reversal of their ion channel blockade. Eur J Pharmacol. 2002 Oct 4;452(2):175-81.
6 Monoamine transporter and sodium channel mechanisms in the rapid pressor response to cocaine. Pharmacol Biochem Behav. 1998 Feb;59(2):305-12.
7 From first class to third class: recent upheaval in antiarrhythmic therapy--lessons from clinical trials. Am J Cardiol. 1996 Aug 29;78(4A):28-33.
8 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
9 Structures of muO-conotoxins from Conus marmoreus. I nhibitors of tetrodotoxin (TTX)-sensitive and TTX-resistant sodium channels in mammalian senso... J Biol Chem. 2004 Jun 11;279(24):25774-82.
10 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
11 Emerging drugs in neuropathic pain. Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26.
12 Heterologous expression and functional analysis of rat Nav1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7-23. Neuropharmacology. 2004 Mar;46(3):425-38.
13 Pathobiology of visceral pain: molecular mechanisms and therapeutic implications. II. Genetic approaches to pain therapy. Am J Physiol Gastrointest Liver Physiol. 2000 Apr;278(4):G507-12.
14 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
15 Antibodies and venom peptides: new modalities for ion channels. Nat Rev Drug Discov. 2019 May;18(5):339-357.
16 Oral Administration of PF-01247324, a Subtype-Selective Nav1.8 Blocker, Reverses Cerebellar Deficits in a Mouse Model of Multiple Sclerosis. PLoS One. 2015; 10(3): e0119067.