918430-49-6

918430-49-6 structure
918430-49-6 structure
  • Name: 3,5-Dichloro-N-((1-((2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl)-4-fluoropiperidin-4-yl)methyl)benzamide
  • Chemical Name: 3,5-Dichloro-N-({1-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl] -4-fluoro-4-piperidinyl}methyl)benzamide
  • CAS Number: 918430-49-6
  • Molecular Formula: C21H29Cl2FN2O2
  • Molecular Weight: 431.37
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2019-01-01 16:00:58
  • Modify Date: 2024-02-02 20:26:41
  • (Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type calcium channel inhibitor) is a potent inhibitor of T-Type calcium channel. TTA-P2 penetrates well the CNS and blocks the native T-type currents in deep cerebellar nuclear neurons, the window current is completely abolished both for wild-type and mutant Cav3.1 channels. TTA-P2 has the potential for the research of neurology disease[1].

Name 3,5-Dichloro-N-({1-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl] -4-fluoro-4-piperidinyl}methyl)benzamide
Synonyms MFCD11977740
Description (Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type calcium channel inhibitor) is a potent inhibitor of T-Type calcium channel. TTA-P2 penetrates well the CNS and blocks the native T-type currents in deep cerebellar nuclear neurons, the window current is completely abolished both for wild-type and mutant Cav3.1 channels. TTA-P2 has the potential for the research of neurology disease[1].
Related Catalog
References

[1]. M R Hellberg, et al. Preclinical efficacy of travoprost, a potent and selective FP prostaglandin receptor agonist. J Ocul Pharmacol Ther. 2001 Oct;17(5):421-32.  

Density 1.25g/cm3
Boiling Point 510.1°C at 760 mmHg
Molecular Formula C21H29Cl2FN2O2
Molecular Weight 431.37
Flash Point 262.3°C
Exact Mass 430.15900
PSA 45.06000
LogP 5.24520
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