General Information of Drug (ID: DMXM19W)

Drug Name
dequalinium Drug Info
Synonyms
dequalinium; Dequadin; 6707-58-0; UNII-E7QC7V26B8; Dequavagyn; Decamine; Labosept; Sorot; GNF-Pf-5483; E7QC7V26B8; CHEBI:41872; Polycidine; Dequavet; Dekadin; Rumilet; Dekamin; Sentril; Sanoral; Oralgol; Ivazil; Dequadin chloride; Dequalin chloride; C30H40N4; DEQ; 1,1'-decane-1,10-diylbis(4-amino-2-methylquinolinium); Solvidont; Quinolinium, 1,1'-(1,10-decanediyl)bis(4-amino-2-methyl-; 1-[10-(4-amino-2-methylquinolyl)decyl]-2-methyl-4-quinolylamine; CHEMBL121663
Indication
Disease Entry ICD 11 Status REF
Myelopathy 8B42 Clinical trial [1]
Cross-matching ID
PubChem CID
2993
ChEBI ID
CHEBI:41872
CAS Number
CAS 6707-58-0
TTD Drug ID
DMXM19W

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Investigative Drug(s)
Discontinued Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
[14C]TEA DM6SFYH Discovery agent N.A. Investigative [6]
EBIO DMPKI0N Discovery agent N.A. Investigative [6]
UCL1684 DMZNJFU Discovery agent N.A. Investigative [7]
DC-EBIO DM2T5OV Discovery agent N.A. Investigative [8]
UCL1848 DM2CN0A Discovery agent N.A. Investigative [7]
apamin DMYNBK5 Discovery agent N.A. Investigative [7]
CyPPA DM64L9I Discovery agent N.A. Investigative [9]
⏷ Show the Full List of 7 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
[14C]TEA DM6SFYH Discovery agent N.A. Investigative [6]
EBIO DMPKI0N Discovery agent N.A. Investigative [6]
UCL1684 DMZNJFU Discovery agent N.A. Investigative [6]
UCL1848 DM2CN0A Discovery agent N.A. Investigative [10]
apamin DMYNBK5 Discovery agent N.A. Investigative [2]
Drug Name Drug ID Indication ICD 11 Highest Status REF
L-(cis)-diltiazem DMK07MI Discovery agent N.A. Investigative [11]
all-trans-retinal DM6CEVB Discovery agent N.A. Investigative [12]
PIP3 DMJX39N Discovery agent N.A. Investigative [13]
Drug Name Drug ID Indication ICD 11 Highest Status REF
zoxazolamine DM70TKB Multiple myeloma 2A83 Terminated [14]
[14C]TEA DM6SFYH Discovery agent N.A. Investigative [6]
EBIO DMPKI0N Discovery agent N.A. Investigative [6]
UCL1684 DMZNJFU Discovery agent N.A. Investigative [2]
DC-EBIO DM2T5OV Discovery agent N.A. Investigative [15]
UCL1848 DM2CN0A Discovery agent N.A. Investigative [16]
apamin DMYNBK5 Discovery agent N.A. Investigative [17]
CyPPA DM64L9I Discovery agent N.A. Investigative [9]
⏷ Show the Full List of 8 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
L-(cis)-diltiazem DMK07MI Discovery agent N.A. Investigative [18]
H-8 DM80QF9 Discovery agent N.A. Investigative [19]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Calcium-activated potassium channel KCa2.1 (KCNN1) TT9R6BE KCNN1_HUMAN Blocker (channel blocker) [2]
Calcium-activated potassium channel KCa2.2 (KCNN2) TT2T5M0 KCNN2_HUMAN Blocker (channel blocker) [3]
Calcium-activated potassium channel KCa2.3 (KCNN3) TT9JH25 KCNN3_HUMAN Blocker (channel blocker) [1]
Cyclic nucleotide-gated channel alpha-1 (CNGA1) TTHIQMC CNGA1_HUMAN Blocker (channel blocker) [4]
Cyclic nucleotide-gated channel alpha-2 (CNGA2) TT8SJGB CNGA2_HUMAN Blocker (channel blocker) [5]

References

1 Pharmacological characterisation of the human small conductance calcium-activated potassium channel hSK3 reveals sensitivity to tricyclic antidepressants and antipsychotic phenothiazines. Neuropharmacology. 2001 May;40(6):772-83.
2 Pharmacological characterization of small-conductance Ca(2+)-activated K(+) channels stably expressed in HEK 293 cells. Br J Pharmacol. 2000 Mar;129(5):991-9.
3 Block of rat brain recombinant SK channels by tricyclic antidepressants and related compounds. Eur J Pharmacol. 2000 Jul 28;401(1):1-7.
4 Dequalinium: a novel, high-affinity blocker of CNGA1 channels. J Gen Physiol. 2003 Jan;121(1):37-47.
5 State-dependent block of CNG channels by dequalinium. J Gen Physiol. 2004 Mar;123(3):295-304.
6 Small conductance calcium-activated potassium channels: from structure to function. Prog Neurobiol. 2010 Jul;91(3):242-55.
7 SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neurones. J Physiol. 2001 Sep 1;535(Pt 2):323-34.
8 Modulators of small- and intermediate-conductance calcium-activated potassium channels and their therapeutic indications. Curr Med Chem. 2007;14(13):1437-57.
9 Selective positive modulation of the SK3 and SK2 subtypes of small conductance Ca2+-activated K+ channels. Br J Pharmacol. 2007 Jul;151(5):655-65.
10 The pharmacology of hSK1 Ca2+-activated K+ channels expressed in mammalian cell lines. Br J Pharmacol. 2000 Feb;129(4):627-30.
11 Primary structure and functional expression of a cyclic nucleotide-activated channel from olfactory neurons. Nature. 1990 Sep 13;347(6289):184-7.
12 All-trans-retinal shuts down rod cyclic nucleotide-gated ion channels: a novel role for photoreceptor retinoids in the response to bright light Proc Natl Acad Sci U S A. 2002 Jun 11;99(12):8372-7.
13 Interplay between PIP3 and calmodulin regulation of olfactory cyclic nucleotide-gated channels. Proc Natl Acad Sci U S A. 2006 Oct 17;103(42):15635-40.
14 Modulation of recombinant small-conductance Ca(2+)-activated K(+) channels by the muscle relaxant chlorzoxazone and structurally related compounds. J Pharmacol Exp Ther. 2001 Mar;296(3):683-9.
15 Specific enhancement of SK channel activity selectively potentiates the afterhyperpolarizing current I(AHP) and modulates the firing properties of ... J Biol Chem. 2005 Dec 16;280(50):41404-11.
16 Calcium-activated potassium channels sustain calcium signaling in T lymphocytes. Selective blockers and manipulated channel expression levels. J Biol Chem. 2001 Apr 13;276(15):12249-56.
17 SK2 encodes the apamin-sensitive Ca(2+)-activated K(+) channels in the human leukemic T cell line, Jurkat. FEBS Lett. 2000 Mar 10;469(2-3):196-202.
18 A new subunit of the cyclic nucleotide-gated cation channel in retinal rods. Nature. 1993 Apr 22;362(6422):764-7.
19 Direct blockade of both cloned rat rod photoreceptor cyclic nucleotide-gated non-selective cation (CNG) channel alpha-subunit and native CNG channels from Xenopus rod outer segments by H-8, a non-specific cyclic nucleotide-dependent protein kinase inhibitor. Neurosci Lett. 1997 Sep 12;233(1):37-40.