TMPH hydrochloride

TMPH hydrochloride Suppliers list
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: Changzhou Chenhong Biotechnology Co., Ltd.  
Tel: +86-0519-85788828 +86-13775037613
Email: sales@chemrenpharm.com
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com

TMPH hydrochloride manufacturers

TMPH hydrochloride Basic information
Product Name:TMPH hydrochloride
Synonyms:TMPH HCl;TMPH hydrochloride solid, (Product is pure based on CHN, NMR and MS results)
CAS:849461-91-2
MF:C16H32ClNO2
MW:305.89
EINECS:
Product Categories:
Mol File:849461-91-2.mol
TMPH hydrochloride Structure
TMPH hydrochloride Chemical Properties
storage temp. 2-8°C
solubility H2O: 22 mg/mL at ~60 °C
form solid
color white
Water Solubility H2O: 22mg/mL at~60°C
InChI1S/C16H31NO2.ClH/c1-6-7-8-9-10-14(18)19-13-11-15(2,3)17-16(4,5)12-13;/h13,17H,6-12H2,1-5H3;1H
InChIKeyXIDDVJIJIFWGIX-UHFFFAOYSA-N
SMILESCl.CCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-43
Safety Statements 26-36/37
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
MSDS Information
TMPH hydrochloride Usage And Synthesis
UsesTMPH Hydrochloride is a potent inhibitor of neuronal AChRs. Therapeutic agent potentially used for the treatment of this progressive neurodegenerative disease such as globoid cell leukodystrophy (GLD) or Krabbe disease.
Biological Activity2,2,6,6-tetramethylpiperidin-4-yl heptanoate (TMPH) is a potent inhibitor of neuronal nicotinic receptors. Evaluation of nicotinic acetylcholine receptor (nAChR) subunits expressed in Xenopus laevis oocytes indicated th at TMPH can produce a potent and long-lasting inhibition of neuronal nAChR formed by the pairwise combination of the most abundant neuronal alpha (i.e., alpha3 and alpha4) and beta subunits (beta2 and beta4), with relatively little effect, because of rapid reversibility of inhibition, on muscle-type (alpha1beta1gammadelta) or alpha7 receptors. However, the inhibition of neuronal beta subunit-containing receptors was also decreased if any of the nonessential subunits alpha5, alpha6, or beta3 were coexpressed. This decrease in inhibition is shown to be associated with a single amino acid present in the second transmembrane domain of these subunits. TMPH abilitty to relate the diverse central nervous system effects to specific nAChR subtypes makes it a useful tool for studying the functional roles of nAChR.
TMPH hydrochloride Preparation Products And Raw materials
Tag:TMPH hydrochloride(849461-91-2) Related Product Information
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