About 10 results found for searched term "82-93-9" (0.055 seconds)
Cat.No. | Name | Target |
---|---|---|
M5487 | Cefdinir | Antibiotic |
FK 482, PD 134393, CI-983 | ||
Cefdinir is an oral cephalosporin antibiotic, used to treat bacterial infections in many different parts of the body. | ||
M7073 | O4I2 | Others |
O4I2 is a oct3/4 inducer; induces expression of pluripotent-associated genes. | ||
M8546 | Chlorcyclizine | Others |
Chlorocyclozine is a first-generation antihistamine compound that is being investigated as a potential hepatitis C agent. | ||
M9605 | Molnupiravir (EIDD-2801) | Anti-infection |
MK-4482; pro-EIDD-1931; CAS#2492423-29-5 | ||
Molnupiravir (EIDD-2801) is an orally bioavailable form of a highly potent ribonucleoside analog that inhibits the replication of multiple RNA viruses including SARS-CoV-2, the causative agent of COVID-19. | ||
M17986 | 3-O-Acetyl-16α-hydroxydehydrotrametenolic acid | Others |
3-O-Acetyl-16α-hydroxydehydrotrametenolic acid | ||
M40660 | Adenosine receptor antagonist 1 | Adenosine Receptor |
Adenosine receptor antagonist 1 is a selective adenosine receptor A2aR antagonist with an IC50 value of 0.29 nM and a 14-fold higher selectivity for A2aR than for A2bR. | ||
M41336 | m-Se3 | c-Myc |
m-Se3 is a potent and selective c-MYC transcription inhibitor that can inhibit tumor growth and has anti-cancer activity. | ||
M41493 | NT160 | HDAC |
NT160 is a highly potent class-IIa HDAC inhibitor with an IC50 value of 0.046 μM. | ||
M41586 | FTX-6746 | PPAR |
FTX-6746 is an orally active PPARG inhibitor. | ||
M57509 | (4S)-N-(TERT-BUTYLDIMETHYLSILYL)AZETIDIN-2-ONE-4-CARBOXYLIC ACID | Others |
(4S)-N-(TERT-BUTYLDIMETHYLSILYL)AZETIDIN-2-ONE-4-CARBOXYLIC ACID |
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