Methoxyphenyl-containing thiophene amide structured double-target-point inhibitor and use thereof
A technology based on acid chlorides and substituents, applied in the field of SGLT2/SGLT1 dual-target inhibitors, can solve the problem of weak SGLT1 inhibitory effect
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Embodiment 1
[0021] The synthesis of embodiment 1 compound I-1
[0022]
[0023] A. Synthesis of Compound V-1
[0024] 4.68g (20mmol) of compound II-1 was dissolved in 10mL of dry dichloromethane, stirred at room temperature, slowly added dropwise 3.81g (30mmol) of freshly distilled oxalyl chloride, and then 2 drops of DMF, and then the reaction mixture was heated at room temperature Stir overnight. The reaction mixture was evaporated to dryness on a rotary evaporator, then dried on a vacuum oil pump for 5 minutes, then dissolved in 10 mL of dichloromethane, stirred under ice-water bath cooling, and then slowly added dropwise 3.10 g (20 mmol) IV-1 and 6.07 g ( 60mmol) triethylamine, after the dropwise addition, the reaction mixture was stirred at room temperature overnight, and TLC was checked for completion of the reaction. After the reaction is complete, pour the reaction mixture into 100mL ice water, stir, and use 50mL×3 CH 2 Cl 2 After extraction, the extract phases were combine...
Embodiment 2-4
[0028] Referring to the operation steps of Example 1, the compounds listed in the following table were synthesized.
[0029]
Embodiment 5
[0030] Inhibition of the compound of Example 5 on human SGLT2 and human SGLT1 in vitro
[0031] Preparation of human SGLT2 expression vector
[0032] The full-length cDNA clone expressing human SGLT2 (purchased from GenScript Company) (with Hind III and Not I sites placed at both ends of the cDNA) was subcloned into the pEAK15 expression vector (Theracos, USA) between the Hind III and Not I sites between. Clones containing the target gene were identified by restriction endonuclease digestion.
[0033] Preparation of human SGLT2 stable transfection cell line
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