1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol-d11

Product Name 1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol-d11
CAT No. CS-T-51421
CAS No. 1189891-05-1
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys C1CCC(CC1)C(CC2=CC=CC=N2)(C3CCC(CC3)OCC4=CC=CC=C4)O
Canonical Smiles C1CCC(CC1)C(CC2=CC=CC=N2)(C3CCC(CC3)OCC4=CC=CC=C4)O
InchIKey WKPUJYYZTNHAGX-MZDFYBDVSA-N
Inchl InChI=1S/C26H35NO2/c28-26(22-11-5-2-6-12-22,19-24-13-7-8-18-27-24)23-14-16-25(17-15-23)29-20-21-9-3-1-4-10-21/h1,3-4,7-10,13,18,22-23,25,28H,2,5-6,11-12,14-17,19-20H2/i2D2,5D2,6D2,11D2,12D2,22D
IUPAC 1-(4-phenylmethoxycyclohexyl)-2-pyridin-2-yl-1-(1,2,2,3,3,4,4,5,5,6,6-undecadeuteriocyclohexyl)ethanol
Controlled No
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1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol-d11 is a deuterated form of 1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol, which is a useful compound in the field of medicinal chemistry. This compound acts as a potent and selective antagonist of the G protein-coupled receptor 40 (GPR40), which is involved in glucose homeostasis and insulin secretion. Due to its pharmacological activity, it has potential therapeutic applications in the treatment of type 2 diabetes and other related metabolic disorders. The deuterated form of this compound, 1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol-d11, is used in pharmacokinetic studies to determine the metabolic fate of the parent compound and to evaluate the bioavailability, distribution, and elimination of the drug in vivo. Deuterium labeling is a commonly used technique in drug development to improve the sensitivity and specificity of analytical methods such as liquid chromatography-mass spectrometry (LC-MS) and nuclear magnetic resonance (NMR) spectroscopy. Chemically, this compound is a chiral molecule with a molecular formula of C23H29D11NO2 and a molecular weight of 385.58 g/mol. It contains one deuterium atom in the hydroxyl group of the ethyl chain, which can be distinguished from the non-deuterated form by mass spectrometry. The synthesis of this compound involves the use of deuterated solvents and reagents to ensure the incorporation of deuterium atoms in the desired positions. Overall, 1-Cyclohexyl-1-(4-benzyloxycyclohexyl)-2-(2-pyridinyl)ethanol-d11 is a valuable tool in drug discovery and development, providing important insights into the pharmacokinetics and pharmacodynamics of GPR40 antagonists.

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