General Information of Drug (ID: DMXR3V4)

Drug Name
KYS-05050 Drug Info
Indication
Disease Entry ICD 11 Status REF
Solid tumour/cancer 2A00-2F9Z Investigative [1]
Cross-matching ID
PubChem CID
135401968
TTD Drug ID
DMXR3V4

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Preclinical Drug(s)
Discontinued Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Sodium bicarbonate DMMU6BJ Metabolic acidosis 5C73 Approved [2]
Flunarizine DMZU5JP Migraine 8A80 Approved [3]
ABT-639 DMEWQ4X Pain MG30-MG3Z Phase 2 [4]
Mibefradil DMU9VDS Glioblastoma multiforme 2A00.0 Phase 1 [5]
TTA-A8 DMWZCIF Insomnia 7A00-7A0Z Preclinical [6]
U-92032 DMTYO3P N. A. N. A. Terminated [7]
ML218 DM3D21X Discovery agent N.A. Investigative [8]
KYS-05001 DM3MID9 Discovery agent N.A. Investigative [9]
KYS-05077 DMHW40F Discovery agent N.A. Investigative [1]
KYS-05080 DM57BXZ Discovery agent N.A. Investigative [1]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Verapamil DMA7PEW Hypertension BA00-BA04 Approved [10]
Ethosuximide DMDZ9LT Epilepsy 8A60-8A68 Approved [11]
Trimethadione DM0Q8MZ Epilepsy 8A60-8A68 Approved [12]
Paramethadione DMR5ZUP Fetal trimethadione syndrome LD2F.0Y Approved [12]
Methsuximide DM6L5VO Epileptic seizures 8A61-8A6Z Approved [13]
Penfluridol DMG1DTE Schizophrenia 6A20 Approved [14]
PD-200390 DMPW28M Insomnia 7A00-7A0Z Phase 2 [15]
NGD 94-1 DMM1Y8F Schizophrenia 6A20 Phase 1 [14]
ML218 DM3D21X Discovery agent N.A. Investigative [8]
KYS-05001 DM3MID9 Discovery agent N.A. Investigative [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 calcium channel alpha Cav3.1 (CACNA1G) TT729IR CAC1G_HUMAN Inhibitor [1]
Voltage-gated calcium channel alpha Cav3.2 (CACNA1H) TTZPWGN CAC1H_HUMAN Inhibitor [1]

References

1 Synthesis and biological evaluation of novel T-type calcium channel blockers. Bioorg Med Chem Lett. 2007 Jan 15;17(2):471-5.
2 Acute renal failure. Clin Evid (Online). 2008 Sep 3;2008. pii: 2001.
3 Positive allosteric interaction of structurally diverse T-type calcium channel antagonists. Cell Biochem Biophys. 2009;55(2):81-93.
4 Effects of a T-type calcium channel blocker, ABT-639, on spontaneous activity in C-nociceptors in patients with painful diabetic neuropathy: a randomized controlled trial. Pain. 2015 Nov;156(11):2175-83.
5 Mibefradil block of cloned T-type calcium channels. J Pharmacol Exp Ther. 2000 Oct;295(1):302-8.
6 Short-acting T-type calcium channel antagonists significantly modify sleep architecture in rodents. ACS Med Chem Lett. 2010 Aug 24;1(9):504-9.
7 Discovery of (2S)-1-(4-amino-2,3,5- trimethylphenoxy)-3-[4-[4-(4- fluorobenzyl)phenyl]-1-piperazinyl]-2-propanol dimethanesulfonate (SUN N8075): a ... J Med Chem. 2000 Sep 7;43(18):3372-6.
8 The Discovery and Characterization of ML218: A Novel, Centrally Active T-Type Calcium Channel Inhibitor with Robust Effects in STN Neurons and in a Rodent Model of Parkinson's Disease. ACS Chem Neurosci. 2011 Dec 21;2(12):730-742.
9 3,4-Dihydroquinazoline derivatives as novel selective T-type Ca2+ channel blockers. Bioorg Med Chem Lett. 2004 Jul 5;14(13):3379-84.
10 Mechanism of tissue-selective drug action in the cardiovascular system. Mol Interv. 2005 Apr;5(2):84-93.
11 Maladaptive homeostatic plasticity in a rodent model of central pain syndrome: thalamic hyperexcitability after spinothalamic tract lesions. J Neurosci. 2008 Nov 12;28(46):11959-69.
12 Prophylactic and therapeutic functions of T-type calcium blockers against noise-induced hearing loss. Hear Res. 2007 Apr;226(1-2):52-60.
13 Block of cloned human T-type calcium channels by succinimide antiepileptic drugs. Mol Pharmacol. 2001 Nov;60(5):1121-32.
14 Differential inhibition of T-type calcium channels by neuroleptics. J Neurosci. 2002 Jan 15;22(2):396-403.
15 Pfizer. Product Development Pipeline. March 31 2009.
16 Discovery of potent T-type calcium channel blocker. Bioorg Med Chem Lett. 2007 Nov 1;17(21):5740-3.