Catalog |
name |
Description |
price |
R-C-2635 |
Pirfenidone CAS:53179-13-8 |
Pirfenidone(AMR69)is an antifibrotic agent that attenuates CCL2 and CCL12 production in fibrocyte cells.Pirfenidone has growth-inhibitory effect and reduces TGF-β2 protein levels in human glioma cell lines.Pirfenidone also has anti-inflammatory activities. |
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R-C-2636 |
A 77-01 CAS:607737-87-1 |
A 77-01 is a potent inhibitor of transforming growth factor(TGF)-β type I receptor superfamily activin-like kinase ALK5 with an IC50 of 25nM. |
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R-C-2637 |
Rottlerin CAS:82-08-6 |
Rottlerin is an angiogenesis inhibitor and an inhibitor of protein kinase Cdelta (PKCdelta)and calmodulin kinase III.Rottlerin induces cyclooxygenase-2 upregulation through an ATF4 and reactive oxygen species-independent pathway in HEI-OC1 cells.Rottlerin exerts its anti-tumor activity through inhibition of Skp2 in breast cancer cells. |
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R-C-2638 |
Bryostatin 1 CAS:83314-01-6 |
Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a potent and central nervous system(CNS)-permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain of Munc13-1 and the full-length Munc13-1 protein with Kis of 8.07nM and 0.45nM,respectively. |
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R-C-2639 |
ZIP CAS:863987-12-6 |
ZIP is a selective peptide inhibitor of PKMζ.ZIP injections can block the impairment in morphine conditioned place preference induced. |
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R-C-2640 |
PPY A CAS:875634-01-8 |
PPY A is a potent inhibitor of T315l mutant and wild-type Abl kinases(IC50 values are 9 and 20nM,respectively).Inhibits growth of cells transformed with either the Bcr-Abl T315l mutant or wild-type Bcr-Abl gene. |
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R-C-2641 |
Bryostatin 2 CAS:87745-28-6 |
Bryostatin 2 is a protein kinase C(PKC)activator. |
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R-C-2642 |
A 83-01 CAS: 909910-43-6 |
A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase,type I nodal receptor ALK4 and type I nodal receptor ALK7,with IC50s of 12nM,45nM and 7.5nM against the transcription induced by ALK5,ALK4 and ALK7,respectively. |
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R-C-3014 |
SB525334 CAS:356559-20-1 |
SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM in a cell-free assay, 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.Only for scientific research, not for human body. |
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