935669-67-3

Usage

Uses

Used in Pharmaceutical Research and Development:
(2S)-2-methylazetidine hydrochloride is used as a synthetic compound for the development of new drugs and pharmaceuticals. Its chiral nature allows it to be used in the synthesis of other chiral molecules, which are essential in creating enantiomer-specific medications.
Used in Synthesis of Chiral Molecules:
(2S)-2-methylazetidine hydrochloride is used as a building block for the synthesis of chiral molecules. Its unique structure enables the creation of enantiomer-specific compounds, which are crucial in the development of targeted and effective pharmaceuticals.
Safety Precautions:
It is important to handle (2S)-2-methylazetidine hydrochloride with caution, as it is a hazardous substance that can cause skin and eye irritation. Proper safety measures should be taken during its use to minimize potential risks.

Upstream product

• 935669-66-2 (S)-tert-butyl 2-methylazetidine-1-carboxylate 
• 77943-38-5 (2R)-4-[(methylsulfonyl)oxy]butan-2-yl methanesulfonate 

Relevant academic research and scientific papers

CHEMICAL COMPOUNDS AS H-PGDS INHIBITORS

A compound of formula (I) wherein R1, R2, R3, R4, X, Y, and A are as defined herein. The compounds of the present invention are inhibitors of hematopoietic prostaglandin D synthase (H-PGDS) and can be useful in the treatment of Duchenne muscular dystrophy. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting H-PGDS activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

SUBSTITUTED 3-AZABICYCLO[3.1.0]HEXANES AS KETOHEXOKINASE INHIBITORS

Provided herein are substituted 3-azabicyclo[3.1.0]hexanes as ketohexokinase inhibitors, processes to make said compounds, and methods comprising administering said compounds to a mammal in need thereof.

TAXANE COMPOUND WITH AZETIDINE RING STRUCTURE

A compound represented by the general formula (1) [X1 and X2 represent hydrogen atom, a halogen atom, hydroxyl group and the like, R1 represents a phenyl group, R2 represents an alkyl group, an alkenyl group, or