Propylamine
Propylamine is a natural product from grape.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Sustainability2021, 13(23),12981.
Horticulturae2022, 8(10), 975.
J Nat Med.2020, 74(1):65-75
Curr Eye Res.2018, 43(1):27-34
Front Nutr.2023, 10:1181135.
LWT2020, 130:109535
LWT2020, 124:109163
bioRxiv-Pharm.&Toxi.2022, 2022.481203.
Front Pharmacol.2020, 11:251.
Hum Exp Toxicol.2017, 36(11):1169-1176
Related and Featured Products
J Gen Physiol. 2015 Jan;145(1):23-45.
Mechanism of activation of the prokaryotic channel ELIC by propylamine: a single-channel study.[Pubmed:
25548135]
METHODS AND RESULTS:
Single-channel currents elicited by the full agonist Propylamine (0.5-50 mM) in outside-out patches at -60 mV were analyzed by direct maximum likelihood fitting of kinetic schemes to the idealized data. Several mechanisms were tested, and their adequacy was judged by comparing the predictions of the best fit obtained with the observable features of the experimental data. These included open-/shut-time distributions and the time course of macroscopic Propylamine-activated currents elicited by fast theta-tube applications (50-600 ms, 1-50 mM, -100 mV). Related eukaryotic channels, such as glycine and nicotinic receptors, when fully liganded open with high efficacy to a single open state, reached via a preopening intermediate.
CONCLUSIONS:
The simplest adequate description of their activation, the "Flip" model, assumes a concerted transition to a single intermediate state at high agonist concentration. In contrast, ELIC open-time distributions at saturating Propylamine showed multiple components.
