2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE

Modify Date: 2024-01-18 17:56:46

2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE Structure
2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE structure
Common Name 2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE
CAS Number 849461-90-1 Molecular Weight 305.88400
Density N/A Boiling Point 356.5ºC at 760 mmHg
Molecular Formula C16H32ClNO2 Melting Point N/A
MSDS N/A Flash Point 169.4ºC

 Use of 2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE


nAChR-IN-1 (2,2,6,6-Tetramethylpiperidin-4-yl heptanoate) is a tetramethylpiperidine heptanoate, a selective nicotinic acetylcholine receptor (nAChR) inhibitor that inhibits nAChRs lacking α5, α6, or β3 subunits. nAChR-IN-1 has the effect of preventing nerve disorder, can be used for nicotinic acetylcholine receptor dysfunction or neurological disorders research[1].

 Names

Name TMPH hydrochloride,2,2,6,6-Tetramethylpiperidin-4-ylheptanoate
Synonym More Synonyms

  Biological Activity

Description nAChR-IN-1 (2,2,6,6-Tetramethylpiperidin-4-yl heptanoate) is a tetramethylpiperidine heptanoate, a selective nicotinic acetylcholine receptor (nAChR) inhibitor that inhibits nAChRs lacking α5, α6, or β3 subunits. nAChR-IN-1 has the effect of preventing nerve disorder, can be used for nicotinic acetylcholine receptor dysfunction or neurological disorders research[1].
Related Catalog
In Vitro nAChR-IN-1 (100 nM) inhibits nAChR with inhibition rate of 90% in Xenovus oocytes, and suppresses AChR subtypes (mouse muscle-type (α1β1εδ) nAChR, three different pairwise combinations of rat neuronal alpha and beta subunits (α3β4, α4β2, and α3β2), and α7 homomeric neuronal nAChR) with IC50s (area) of 390, 1.2, 110, 75, 440, 460, 430, 2.7, 1.0, 1.4, and 18.3 nM, respectively, based on the decrease in the net charge of the ACh response[1].
In Vivo nAChR-IN-1 (20 mg/kg; s.c.; single dose) improves nicotine-induced hypomotility and hypothermia in a time-dependent manner in mice[1]. Animal Model: Nicotine-induced mice model[1] Dosage: 20 mg/kg Administration: Subcutaneous injection; single dose; 15 minutes prior to the injection of nicotine (1.5 mg/kg)  Result: Increased locomotor activity in mice, even if nicotine-induced decrease. Showed no effect on body temperature. Animal Model: Tail-flick and hot-platemodel in mice[1] Dosage: 0, 0.1, 1, 5 mg/kg Administration: Subcutaneous injection; single dose Result: Blocked the antinociceptive effect of nicotine in the hot-plate. Time-dependently blocked nicotine-induced antinociception.
References

[1]. Papke RL, et, al. Compositions et methodes d'inhibition selective des recepteurs nicotiniques de l'acetylcholine. WO2005032479A2

 Chemical & Physical Properties

Boiling Point 356.5ºC at 760 mmHg
Molecular Formula C16H32ClNO2
Molecular Weight 305.88400
Flash Point 169.4ºC
Exact Mass 305.21200
PSA 38.33000
LogP 4.94000

 Safety Information

Hazard Codes Xi: Irritant;
Risk Phrases 36/37/38-43
Safety Phrases 26-36/37

 Synonyms

2,2,6,6-TETRAMETHYLPIPERIDIN-4-YL HEPTANOATE HYDROCHLORIDE
TMPH HYDROCHLORIDE
2,2,6,6-Tetramethylpiperidin-4-ylheptanoate
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