About 6 results found for searched term "66-71-7" (0.302 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M7131 | Phenanthroline | Others |
| 1,10-Phenanthroline; o-Phenanthroline | ||
| Phenanthroline is a compound that promotes differentiation of hPSC into cranial lamina cells. | ||
| M20611 | MK571 | Others |
| L-660711, L660711, MK-571, MK 571 | ||
| MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor) antagonist. | ||
| M41930 | PAT-IN-1 | Ras |
| PAT-IN-1 is a protein acyl transferases (PAT) inhibitor. | ||
| M42696 | KSK94 | Sigma Receptor |
| KSK94 is a high-affinity histamine H3 receptor antagonist, with Kis of 7.9, 2958, 75.2 nM for H3 receptor, sigma-1, sigma-2 receptor respectively. | ||
| M20715 | CS-2660 (JNJ-38158471) | VEGFR/PDGFR |
| CS-2660 (JNJ-38158471) is a well tolerated, orally available, highly selective VEGFR-2 inhibitor with IC50 of 40 nM. CS-2660 (JNJ-38158471) also inhibits closely related tyrosine kinases such as Ret and Kit with IC50 of 180 nM and 500 nM，while it has no significant activity (>1 microM) against VEGFR-1 and VEGFR-3. | ||
| M28634 | PF-06648671 | Gamma-secretase/Beta-secretase |
| PF-06648671 is a novel, brain-penetrable, and orally active γ-secretase modulator (GSM). PF-06648671 reduces Aβ42 and Aβ40, with concomitant increases in Aβ37 and Aβ38 in vitro. PF-06648671 is used for the study of Alzheimer’s disease. | ||
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