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Merck
CN

SML3223

CAY10566

≥98% (HPLC)

Synonym(s):

2-(6-(4-(2-Chloro-5-fluorophenoxy)piperidin-1-yl)pyridazin-3-yl)-5-methyl-1,3,4-oxadiazole, Abbott compound 74, Abbott-28c, CAY 10566, CAY-10566, SCD1 inhibitor 28c

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About This Item

Empirical Formula (Hill Notation):
C18H17ClFN5O2
CAS Number:
944808-88-2
Molecular Weight:
389.81
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
MFCD11976899

Key Documents

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SMILES string

Fc1cc(c(cc1)Cl)OC2CCN(CC2)c3nnc(cc3)c4nnc([o]4)C

InChI

1S/C18H17ClFN5O2/c1-11-21-24-18(26-11)15-4-5-17(23-22-15)25-8-6-13(7-9-25)27-16-10-12(20)2-3-14(16)19/h2-5,10,13H,6-9H2,1H3

InChI key

WFOFPVXMPTVOTJ-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

off-white to orange

solubility

DMSO: 2 mg/mL, clear (warmed)

storage temp.

2-8°C

Quality Level

100

Related Categories

Biochem/physiol Actions

CAY10566 is a potent and selective stearoyl-CoA desaturase 1 (SCD1) inhibitor (IC50 = 26 nM/hSCD1 and 4.5 nM/mSCD1; IC50 >10 μM/75 receptors, transporters, ion channels). CAY10566 effectively blocks the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC50 = 7.9 nM by C17:1/C17:0 ratio; IC50 = 6.8 nM by C16:1/C16:0 ratio) and exhibits good metabolic stability (by rat & mouse liver microsome assays) and oral availability (rat F = 59.2%; 5 mg/kg p.o.). CAY10566 is typically used in the range from 0.1-10 μM for cell treatment.
Orally available, potent and selective stearoyl-CoA desaturase 1 (SCD1) inhibitor.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000427899
0000427899
0000241341
0000241341
0000143126

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