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 About 11 results found for searched term "50-57-7" (0.06 seconds)

Cat.No.  Name Target
M1777 SGX523 c-Met
SGX523 is an exquisitely selective, ATP-competitive inhibitor of the MET receptor tyrosine kinase with antitumor activity in vivo.
M4295 Tenacissoside-X Others
Tenacissoside-X
M8112 PF-05085727 Others
PF-05085727 is a potent inhibitor against cGMP-dependent phosphodiesterase PDE2 (PDE2A; IC50 = 2.
M11158 Cyclo(-RGDfK) TFA Integrin
Cyclo(-RGDfK) TFA is a potent, selective integrin αvβ3 INHIBITORS, THEIR IC50 The value is 0.94 nM. Cyclo(-RGDfK) TFA specifically targets tumor microvascular and cancer cells by binding to αvβ3 integrins on the cell surface.
M20343 WAY-299359 FLT3
WAY-299359 is a FLT3 inhibitor
M21533 BI-0474 Ras
BI-0474 is a covalent KRASG12C inhibitor. The IC50 value for GDP-KRAS::SOS1 protein-protein interaction was 7.0 nM. BI-0474 also showed better antitumor activity in non-small cell lung cancer xenograft models.
M25195 Efprezimod alfa Others
Efprezimod alfa is an active peptide. Efprezimod alfa can be used for various biochemical studies.
M29337 ARN19874  Phospholipase
ARN19874 is a selective, reversible uncompetitive N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) activity inhibitor with an IC50 of ~34 μM.
M30203 Lysipressin Adenylate Cyclase
Lysine vasopressin; [Lys8]-Vasopressin
Lysipressin (Lysine vasopressin) is antidiuretic hormone that have been found in pigs and some marsupial families. Lysipressin induces contraction of the rabbit urinary bladder smooth muscle, activate adenylate-cyclase.
M51744 H-Phe-Gly-His-p-nitro-Phe-Phe-Ala-Phe-OMe Others
H-Phe-Gly-His-p-nitro-Phe-Phe-Ala-Phe-OMe is a polypeptide that can be hydrolyzed by Rennin.
M52171 (S)-3-Amino-4-hydroxybutanoic acid Amino Acid Derivatives
(S)-3-Amino-4-hydroxybutanoic acid is a serine derivative.



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