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MK6-83

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MK6-83
Identifiers
  • 5-methyl-N-[2-(piperidin-1-yl)phenyl]thiophene-2-sulfonamide
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H20N2O2S2
Molar mass336.47 g·mol−1
3D model (JSmol)
  • CC1=CC=C(S1)S(=O)(=O)NC2=CC=CC=C2N3CCCCC3
  • InChI=1S/C16H20N2O2S2/c1-13-9-10-16(21-13)22(19,20)17-14-7-3-4-8-15(14)18-11-5-2-6-12-18/h3-4,7-10,17H,2,5-6,11-12H2,1H3
  • Key:IRGYSXZCDAWOOC-UHFFFAOYSA-N

MK6-83 is a chemical compound which acts as a channel opener for theTRPML family of calcium channels, with moderate selectivity forTRPML1 over the relatedTRPML2 andTRPML3 subtypes.[1][2][3]

See also

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References

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  1. ^Kilpatrick BS, Yates E, Grimm C, Schapira AH, Patel S (October 2016)."Endo-lysosomal TRP mucolipin-1 channels trigger global ER Ca2+ release and Ca2+ influx".Journal of Cell Science.129 (20):3859–3867.doi:10.1242/jcs.190322.PMC 5087663.PMID 27577094.
  2. ^Morelli MB, Amantini C, Tomassoni D, Nabissi M, Arcella A, Santoni G (April 2019)."Transient Receptor Potential Mucolipin-1 Channels in Glioblastoma: Role in Patient's Survival".Cancers.11 (4).doi:10.3390/cancers11040525.PMC 6521337.PMID 31013784.
  3. ^Xia Z, Wang L, Li S, Tang W, Sun F, Wu Y, et al. (October 2020). "ML-SA1, a selective TRPML agonist, inhibits DENV2 and ZIKV by promoting lysosomal acidification and protease activity".Antiviral Research.182 104922.doi:10.1016/j.antiviral.2020.104922.PMID 32858116.
TRPA
Activators
Blockers
TRPC
Activators
Blockers
TRPM
Activators
Blockers
TRPML
Activators
Blockers
TRPP
Activators
Blockers
TRPV
Activators
Blockers
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