ChemicalBook--->CAS DataBase List--->136186-07-7

136186-07-7

136186-07-7 Structure

136186-07-7 Structure
IdentificationBack Directory
[Name]

2-Propenamide, 2-cyano-3-(3,5-dichlorophenyl)-3-hydroxy-N-[4-(trifluoromethyl)phenyl]-
[CAS]

136186-07-7
[Synonyms]

TPC2-A1-N
2-Propenamide, 2-cyano-3-(3,5-dichlorophenyl)-3-hydroxy-N-[4-(trifluoromethyl)phenyl]-
[Molecular Formula]

C17H9Cl2F3N2O2
[MDL Number]

MFCD32878270
[MOL File]

136186-07-7.mol
[Molecular Weight]

401.17
Chemical PropertiesBack Directory
[Boiling point ]

536.9±50.0 °C(Predicted)
[density ]

1.546±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

5.05±0.60(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

TPC2-A1-N is a powerful and Ca2+-permeable agonist of?two pore?channel?2?(TPC2), which plays its role by mimicking the physiological actions?of?NAADP. TPC2-A1-P reproducibly?evokes significant Ca2+ responses from TPC2 (EC50=7.8 μM), and the effect can be blocked by several TPC blockers. TPC2-A1-N can be used to probe different functions of TPC2 channels in intact cells[1][2].
[Biological Activity]

TPC2-A1-N is a selective two pore segment channel 2 (TCP2) agonist th at mimics the action of NAADP where it selectively induces fast Ca2+ signals (EC50 = 7.8 μM) in a TCP2-dependent mannerwithout potency toward TRPML1/2/3. In contrastTPC2-A1-N is a much weaker Na+ current inducer when compared to PI(3,5)P2 and TPC2-A1-P. TPC2-A1-Nbut not the Na+ signals agonist TPC2-A1-P causes TPC2-dependent alkalinization of lysosomal lumen Ca2+ stores (10 μMTPC2-expressing HeLa cells)while TPC2-A1-Pbut not TPC2-A1-Nactivates TPC2-dependent lysosomal exocytosis (30 μMmurine macrophages).
[References]

[1] Susanne Gerndt, et al. Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal function. Elife DOI:10.7554/eLife.54712
[2] Xuhui Jin, et al. Targeting Two-Pore Channels: Current Progress and Future Challenges. Trends Pharmacol Sci. 2020 Aug;41(8):582-594. DOI:10.1016/j.tips.2020.06.002
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