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AM 92016 hydrochloride

CAS No.
133229-11-5
Chemical Name:
AM 92016 hydrochloride
Synonyms
AM92016,Inhibitor,inhibit,AM 92016,AM 92016 hydrochloride,AM92016 hydrochloride,AM-92016;N-[4-[3-[[2-(3,4-Dichlorophenyl)ethyl]methylamino]-2-hydroxypropoxy]phenyl]methanesulfonamide hydrochloride
CBNumber:
CB14806425
Molecular Formula:
C19H25Cl3N2O4S
Molecular Weight:
483.83
MDL Number:
MOL File:
133229-11-5.mol
Last updated:2023-09-20 16:43:00

AM 92016 hydrochloride Properties

storage temp. 4°C, protect from light
solubility <48.38mg/ml in DMSO; <24.19mg/ml in H2O
form solid
color White

AM 92016 hydrochloride price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC A634675 AM92016Hydrochloride 133229-11-5 1mg $105 2021-12-16 Buy
ApexBio Technology B6482 AM92016hydrochloride 133229-11-5 5mg $158 2021-12-16 Buy
ApexBio Technology B6482 AM92016hydrochloride 133229-11-5 10mg $284 2021-12-16 Buy
ApexBio Technology B6482 AM92016hydrochloride 133229-11-5 50mg $929 2021-12-16 Buy
DC Chemicals DC26176 AM92016 133229-11-5 100mg $600 2021-12-16 Buy
Product number Packaging Price Buy
A634675 1mg $105 Buy
B6482 5mg $158 Buy
B6482 10mg $284 Buy
B6482 50mg $929 Buy
DC26176 100mg $600 Buy

AM 92016 hydrochloride Chemical Properties,Uses,Production

Biological Activity

am 92016 hydrochloride is a specific inhibitor of delayed rectifier potassium current [1].potassium channel is an ion channel and acts to reset the resting potential and shapes the action potential. delayed rectifier potassium channel (ik) is activated by the influx of na+ and discharges k+, which repolarizes the membrane. ik restricts the duration of the nerve impulse.am 92016 hydrochloride is a specific ik inhibitor. in guinea-pig and rabbit ventricular cells, am 92016 significantly increased action potential duration with 20% and 90% repolarization levels, respectively. also, am 92016 (1 μm) inhibited ik activated by step depolarizations in a time-dependent way [1]. in rabbit sino-atrial node cells, am 92016 (50 nm) significantly inhibited ik with ic50 value of 40 nm in a concentration-dependent way [2]. in vascular smooth muscle cells (vsmc), am92016 hydrochloride inhibited no-induced erk1/2 dephosphorylation [3].in guinea-pigs, am 92016 (1-5 mg/kg) significantly increased heart rate, left ventricular systolic pressure, systolic arterial blood pressure and the contractile index dp dtmax. am 92016 exhibited proarrhythmic activity [4].

References

[1]. connors sp, gill ew, terrar da. actions and mechanisms of action of novel analogues of sotalol on guinea-pig and rabbit ventricular cells. br j pharmacol, 1992, 106(4): 958-965.
[2]. lei m, brown hf. inhibition by compound ii, a sotalol analogue, of delayed rectifier current (ik) in rabbit isolated sino-atrial node cells. naunyn schmiedebergs arch pharmacol, 1998, 357(3): 260-267.
[3]. palen di, belmadani s, lucchesi pa, et al. role of shp-1, kv.1.2, and cgmp in nitric oxide-induced erk1/2 map kinase dephosphorylation in rat vascular smooth muscle cells. cardiovasc res, 2005, 68(2): 268-277.
[4]. hagerty mj, wainwright cl, kane ka. the in-vivo cardiovascular effects of a putative class iii anti-arrhythmic drug, am 92016. j pharm pharmacol, 1996, 48(4): 417-421.

AM 92016 hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

AM 92016 hydrochloride Suppliers

Global( 35)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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InvivoChem
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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 025-66113011 18112977050 cb6@aikonchem.com China 16687 50
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AM 92016 hydrochloride Spectrum

N-[4-[3-[[2-(3,4-Dichlorophenyl)ethyl]methylamino]-2-hydroxypropoxy]phenyl]methanesulfonamide hydrochloride AM92016,Inhibitor,inhibit,AM 92016,AM 92016 hydrochloride,AM92016 hydrochloride,AM-92016 133229-11-5