31339-06-7

Upstream product

• 5333-40-4 2-isopropyl-5-methylphenoxyacetic acid 
• 89-83-8 thymol 

Downstream Products

• 135508-99-5 (3S,4R)-4-Benzo[1,3]dioxol-5-yl-3-(2-isopropyl-5-methyl-phenoxy)-1-phenyl-azetidin-2-one 
• 135509-05-6 (3R,4S)-1-Benzo[1,3]dioxol-5-ylmethyl-3-(2-isopropyl-5-methyl-phenoxy)-4-(4-methoxy-phenyl)-azetidin-2-one 
• 135509-02-3 (3R,4S)-4-Benzo[1,3]dioxol-5-yl-1-(3,4-dimethoxy-benzyl)-3-(2-isopropyl-5-methyl-phenoxy)-azetidin-2-one 
• 135509-07-8 (3R,4S)-4-Benzo[1,3]dioxol-5-yl-1-benzo[1,3]dioxol-5-ylmethyl-3-(2-isopropyl-5-methyl-phenoxy)-azetidin-2-one 
• 100289-61-0 (3S,4R)-3-(2-Isopropyl-5-methyl-phenoxy)-1-(4-methoxy-phenyl)-4-phenyl-azetidin-2-one 
• 111719-46-1 2-((Ξ)-4-dimethylamino-benzylidene)-7-isopropyl-4-methyl-benzofuran-3-one 
• 97282-07-0 <3-Methyl-6-isopropyl-phenoxy>-essigsaeure- 
• 97804-99-4 <3-Methyl-6-isopropyl-phenoxy>-essigsaeure- 
• 100289-58-5 (3S,4R)-3-(2-Isopropyl-5-methyl-phenoxy)-1,4-diphenyl-azetidin-2-one 
• 135509-03-4 (3R,4S)-1-Benzo[1,3]dioxol-5-ylmethyl-3-(2-isopropyl-5-methyl-phenoxy)-4-phenyl-azetidin-2-one 

Relevant academic research and scientific papers

PEPTIDES, COMPOUNDS, COMPOSITIONS AND METHODS FOR INHIBITING SOX9 DIMERIZATION

The present application provides SOX9 dimerization inhibitor compounds, compositions, and methods of use thereof. In certain aspects, the SOX9 dimerization inhibitor is a peptide comprising a portion of the SOX9 dimerization motif and a TAT protein to support cell entry which is c-terminal to the SOX9 dimerization motif as set forth in SEQ ID NO:3. In other aspects, the SOX9 dimerization inhibitor is a compound of the general formula I (The applicant is kindly asked to please insert chemical structure here) where one A is H and the other is: (please insert second chemical structure here), and the remaining substituents are as defined in the application.

Synthesis of Monocyclic β-Lactams with a Terpenoid Moiety

A series of new monocyclic β-lactams with a terpenoid moiety have been prepared by reaction of schiff bases with appropriate terpenyl acid chlorides in the presence of triethylamine.Their structural assignments are based on elemental analyses and spectral