Metformin/pioglitazone

Resomelagon (AP1189) acetate is a potent, orally active melanocortin receptor (MR) agonist about MC 1 and MC 3 . Resomelagon acetate induces ERK1/2 phosphorylation and Ca 2+ mobilization. Resomelagon acetate has anti-inflammatory activity.

Resomelagon (AP1189) acetate is a potent, orally active melanocortin receptor (MR) agonist about MC 1 and MC 3 . Resomelagon acetate induces ERK1/2 phosphorylation and Ca 2+ mobilization. Resomelagon acetate has anti-inflammatory activity.

Resomelagon (AP1189) acetate is a potent, orally active melanocortin receptor (MR) agonist about MC 1 and MC 3 . Resomelagon acetate induces ERK1/2 phosphorylation and Ca 2+ mobilization. Resomelagon acetate has anti-inflammatory activity.

Biochem/physiol Actions SC-57461A is an inhibitor of leukotriene A4 hydrolase. Other Notes This compound was developed by Pfizer for Lipid Signaling research .

Biochem/physiol Actions SC-57461A is an inhibitor of leukotriene A4 hydrolase. Other Notes This compound was developed by Pfizer for Lipid Signaling research .

Product introductionSF1670 is a potent and specific phosphatase and tensin homolog deleted on chromosome 10 (PTEN) inhibitorApplicationSF1670 has been used:• To study the effect of microRNA-30a on PTEN (phosphatase and tensin homologue deleted on

General description SMAD1 is a member of the SMAD family which are signal transducers and transcriptional modulators that mediate multiple signaling pathways. The actions of bone morphogenetic proteins (BMPs) are mediated by SMAD1 and SMAD1 can be

A selective inhibitor of TGF-&beta and activin signaling that suppresses SMAD3 phosphorylation (IC₅₀ = 3 &microM) reduces TGF-&beta1-induced type 1 procollagen expression and myofibroblast differentiation in normal dermal fibroblasts

A selective inhibitor of TGF-&beta and activin signaling that suppresses SMAD3 phosphorylation (IC₅₀ = 3 &microM) reduces TGF-&beta1-induced type 1 procollagen expression and myofibroblast differentiation in normal dermal fibroblasts

SMIFH2 Formin FH2 Domain Inhibitor.

Smurf1 is a member of the Nedd4-like family of E3 ligases. It contains an amino terminal C2 domain and 2 WW domains that are responsible for cellular localization and substrate recognition, and a catalytic carboxyl terminal HECT domain.

Smurf1 is a member of the Nedd4-like family of E3 ligases. It contains an amino terminal C2 domain and 2 WW domains that are responsible for cellular localization and substrate recognition, and a catalytic carboxyl terminal HECT domain.