Catalog |
name |
Description |
price |
R-C-2611 |
SC-10 CAS:102649-79-6 |
SC-10 is a PKC activator.It acts by stimulating PKC mediated myosin light chain phosphorylation without activating MLC kinase. |
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R-C-2612 |
ML347 CAS:1062368-49-3 |
ML347(DN193719)is a highly selective ALK1/ALK2 inhibitor with IC50s of 46/32nM; shows>300-fold selectivity for ALK2 vs. |
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R-C-2613 |
SR-3677 CAS:1072959-67-1 |
SR-3677 is a novel,potent and highly selective inhibitor of Rho Kinase(ROCK-II) with the IC50 value of ~0.3nM in enzyme and cell based assays. |
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R-C-2614 |
DMH-1 CAS:1206711-16-1 |
DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/107.9/<5/47.6 nM for ALK1/ALK2/ALK3/ALK6,respectively. |
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R-C-2616 |
Calphostin C CAS:121263-19-2 |
The calphostins are a class of closely related chemical compounds isolated from the fungus Cladosporium cladosporioides.The known calphostins include calphostin A,calphostin B,calphostin C,calphostin D,and calphostin I.The calphostins are inhibitors of protein kinase C(PKC). |
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R-C-2617 |
PKC fragment (530-558) |
Potent activator of protein kinase C(Ka~10 mM);corresponds to residues 530-558 of the catalytic domain of PKC. |
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R-C-2618 |
Ro 31-8220 Mesylate CAS:138489-18-6 |
Ro 31-8220 is a PKC-inhibitor,which inhibits stimulated fluid pinocytosis of human PMNs induced by the PKC-activators phorbol myristate acetate (PMA,IC50=1.35 x 10(-6)M)or diacylglycerols(OAG,diC8)by 95%.Ro-31-8220 showed the apoptotic effect on HL-60 cells,which was mediated by a well-characterized transduction process of apoptotic signals:i.e.,mitochondrial cytochrome c efflux and the activation of caspase-3 in the cytosol. |
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R-C-2620 |
Vactosertib (TEW-7197) CAS:1352608-82-2 |
Vactosertib(EW-7197)is a potent,orally active and ATP-competitive activin receptor-like kinase 5(ALK5)inhibitor with an IC50 of 12.9nM.Vactosertib also inhibits ALK2 and ALK4(IC50 of 17.3nM)at nanomolar concentrations.Vactosertib has potently antimetastatic activity and anticancer effect. |
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R-C-2621 |
LDN-212854 CAS:1432597-26-6 |
LDN-212854 is a novel BMP inhibitor that exhibits substantially greater selectivity for BMP versus the TGF-β type I receptors;possesses a bias towards ALK2(IC50=1.3nM)versus ALK1 and ALK3 compared to other inhibitors. |
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R-C-2622 |
CGP 53353 CAS:145915-60-2 |
Selective inhibitor of PKCβII(IC50 values are 0.41 and 3.8μM for PKCβII and PKCβI respectively).Also inhibits prionogenic Sup35 fibrillization (IC50~ 3.4μM)and inhibits de novo Aβ42 assembly in vitro. |
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