About 5 results found for searched term "GF109" (0.119 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2975 | RG2833 | HDAC |
| RGFP109 | ||
| RG2833 (RGFP109) is a brain-penetrant HDAC inhibitor with IC50 of 60 nM and 50 nM for HDAC1 and HDAC3, respectively. | ||
| M3802 | GF 109203X | PKC |
| GO 6850; Bisindolylmaleimide I | ||
| GF 109203X is a very potent and selective inhibitor of protein kinase C, selective for the α and β1 isoforms (IC50 values are 0.0084, 0.0180, 0.210, 0.132, and 5.8 μM for α, β1, δ, ε and ζ isoforms respectively). | ||
| M7644 | GF 109203X hydrochloride | Others |
| Inhibitor of protein kinase C; potent inhibitor of GSK-3. | ||
| M52674 | GF109 | ACE |
| GF109 is a potent parenteral inhibitor of angiotensin converting enzyme (ACE). | ||
| M11496 | FGF-basic, Rat (E. coli) | Cytokines and Growth Factors |
| Fibroblast Growth Factor-basic; FGF-2; BFGF; FGFB; HBGF-2; bFGF; Prostatropin | ||
| FGF-basic, Rat（E. coli） Expressed with an n-terminal Gly. FGF-basic (Pro10-Ser154) Accession # P13109. Bioactivity: ED50 < 0.25 ng/ mL, measured by 3T3 cell proliferation method, corresponding to > 4.0 × 106 units /mg. | ||
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