LY2940094 tartrate|CAS 1307245-87-9|DC Chemicals

Cas No.:	1307245-87-9
Chemical Name:	LY-2940094 tartrate
Synonyms:	(2-(4-((2'-chloro-4',4'-difluoro-4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran]-1-yl)methyl)-3-methyl-1H-pyrazol-1-yl)pyridin-3-yl)methanol (2R,3R)-2,3-dihydroxysuccinate;1307245-87-9 (Tartrate);[2-[4-[(2-chloro-4,4-difluorospiro[5H-thieno[2,3-c]pyran-7,4'-piperidine]-1'-yl)methyl]-3-methylpyrazol-1-yl]pyridin-3-yl]methanol;(2R,3R)-2,3-dihydroxybutanedioic acid;1307245-87-9;CQKWYQOOVWQULQ-LREBCSMRSA-N;AKOS040748839;HY-114452A;LY2940094 (tartrate);AC-36289;LY-2940094 tartrate;G66504;CS-0085529;EX-A3004A
SMILES:	ClC1=CC2C(COC3(C=2S1)CCN(CC1=CN(C2C(=CC=CN=2)CO)N=C1C)CC3)(F)F.O[C@@H](C(=O)O)[C@H](C(=O)O)O
Formula:	C₂₆H₂₉ClF₂N₄O₈S
M.Wt:	631.045271635056
Purity:	98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

MSDS

COA

Cat. No.	Product name	Field of application
DC46693	DAMGO	DAMGO (DAGO) is a potent and selective μ opioid receptor agonist with ki of 17 nM.
DC44976	LY2940094 tartrate	LY2940094 (BTRX-246040) tartrate is a potent, brain penetrant, selective and orally available N/OFQ peptide (NOP) receptor antagonist with high affinity (Ki=0.105 nM) and antagonist potency (Kb=0.166 nM). LY2940094 tartrate reduces Ethanol self-administration and Ethanol seeking in animal models.
DC28780	LY2444296	LY2444296 is an orally bioavailable, high-affinity and selective short-acting kappa opioid receptor (KOPR) antagonist, with a Ki value of ∼1 nM. LY2444296 exhibits anti-anxiety like effects.
DC10290	PZM21	PZM21 is a potent and selective μ opioid receptor agonist with an EC50 of 1.8 nM.
DC9527	Methylnaltrexone (Bromide)	Methylnaltrexone Bromide is a pheriphally-acting μ-opioid antagonist that acts on the gastrointestinal tract to decrease opioid-induced constipation.
DC9526	Meptazinol (hydrochloride)	Meptazinol Hcl(WY-22811 Hcl) is a unique centrally active opioid analgesic.
DC7050	ADL5859 HCl	ADL5859 agonizes δ-opioid receptor with a 1000-fold selectivity than µ- or κ-opioid receptor with Ki of 32 nM and 37 nM, respectively.ADL5859 displays weak inhibitory activity at the hERG channel with an IC50 of 78 μM. The EC50 of ADL5859 against δ opioid