[Ala17]-MCH TFA|CAS 0|DC Chemicals

Cas No.:
Chemical Name:	[Ala17]-MCH TFA
Synonyms:	DFDMLRCMLGRVYRPCAQV (Disulfide bridge:Cys7-Cys16)
Formula:	C₉₉H₁₅₆F₃N₂₉O₂₈S₄
M.Wt:	2385.73
Purity:	>98%
Sotrage:	Please store the product under the recommended conditions in the Certificate of Analysis.

MSDS

COA

Cat. No.	Product name	Field of application
DC43987	MCHR1 antagonist 2	MCHR1 antagonist 2 is an antagonist of melanin concentrating hormone receptor 1, with an IC50 of 65 nM; MCHR1 antagonist 2 also inhibits hERG, with an IC50 of 4.0 nM in IMR-32 cells.
DC41656	[Ala17]-MCH TFA	[Ala17]-MCH TFA, a MCH analogue, is a selective ligand for MCHR1 (Ki=0.16 nM) over MCHR2 (Ki=34 nM). [Eu3+ chelate-labeled [Ala17]-MCH shows high affnity for MCHR1 (Kd=0.37 nM) while has little demonstrable binding affnity for MCHR2.
DC41655	[Ala17]-MCH	[Ala17]-MCH, a MCH analogue, is a selective ligand for MCHR1 (Ki=0.16 nM) over MCHR2 (Ki=34 nM). [Eu3+ chelate-labeled [Ala17]-MCH shows high affnity for MCHR1 (Kd=0.37 nM) while has little demonstrable binding affnity for MCHR2.
DC28204	SNAP 94847 hydrochloride	SNAP 94847 hydrochloride is a novel, high affinity selective melanin-concentrating hormonereceptor1 (MCHR1) antagonist with (Ki= 2.2 nM, Kd=530 pM), it displays >80-fold and >500-fold selectivity over MCHα1A and MCHD2 receptors respectively. SNAP 94847 hydrochloride binds with high affinity to the mouse and rat MCHR1 with minimal cross-reactivity to other GPCR, ion channels, enzymes, and transporters.