| Identification | Back 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 Properties | Back 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 | [SMILES]
O=C(/C(C#N)=C(O)/C1=CC(Cl)=CC(Cl)=C1)NC2=CC=C(C=C2)C(F)(F)F |
| Hazard Information | Back 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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Merck KGaA
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www.sigmaaldrich.cn |
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MedChemExpress
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www.medchemexpress.com |
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