About 10 results found for searched term "94-09-7" (0.053 seconds)
Cat.No. | Name | Target |
---|---|---|
M2039 | Baricitinib | JAK |
INCB28050, LY3009104 | ||
Baricitinib (INCB28050) is an oral JAK1 and JAK2 inhibitor with IC50 of 5.9 nM and 5.7 nM, respectively. | ||
M2442 | Benzocaine | Animal experimental anesthetics |
Benzocaine is the ethyl ester of p-aminobenzoic acid (PABA), it is a local anesthetic commonly used for the research of topical pain reliever or in cough drops. Benzocaine shares a common receptor with all othe rLAs in the voltage-gated Na+ channel, with an IC50 of 0.8 mM tested with a potential of +30 mV. | ||
M5218 | AZ191 | Others |
AZ191 is a potent small molecule inhibitor that selectively inhibits DYRK1B in vitro and in cells. | ||
M10071 | KO-947 | ERK |
KO947; K0947 | ||
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. | ||
M18591 | Aristolactam BII | Others |
Aristolactam BII | ||
M28534 | NE-100 hydrochloride | Sigma Receptor |
NE-100 (hydrochloride) is a potent and selective sigma-1 receptor antagonist with an IC50 of 4.16 nM. NE-100 (hydrochloride) exerts antipsychotic activity in vivo. NE-100 (hydrochloride) also suppresses ER stress-induced hippocampal cell death. | ||
M30944 | Mericitabine | Anti-infection |
RG 7128; R-7128; PSI 6130 diisobutyrate | ||
Mericitabine (RG 7128; R-7128) is a nucleoside inhibitor of the HCV NS5B polymerase that acts as an RNA chain terminator and prevents elongation of RNA transcripts during replication. | ||
M52853 | Acetyl hexapeptide-49 | IL Receptor/Related |
Acetyl hexapeptide-49 is a bioactive peptide with anti-allergen effect and has been reported used as a cosmetic ingredient. | ||
M56982 | Phytosterols | Others |
Phytosterols are anticancer agents. | ||
M58231 | CMP-5 dihydrochloride | Histone Methyltransferase |
CMP-5 2HCl | ||
CMP-5 dihydrochloride is a potent, specific, and selective PRMT5 inhibitor, while displays no activity against PRMT1, PRMT4, and PRMT7 enzymes. CMP-5 dihydrochloride selectively blocks S2Me-H4R3 by inhibiting PRMT5 methyltransferase activity on histone preparations. |
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