Top Suppliers:I want be here

765914-60-1

765914-60-1 structure
765914-60-1 structure
  • Name: Emprumapimod
  • Chemical Name: Emprumapimod
  • CAS Number: 765914-60-1
  • Molecular Formula: C24H29F2N5O3
  • Molecular Weight: 473.52
  • Catalog: Signaling Pathways MAPK/ERK Pathway p38 MAPK
  • Create Date: 2022-05-22 12:30:31
  • Modify Date: 2024-01-17 16:54:27
  • Emprumapimod is a potent, orally bioavailable and selective inhibitor of p38α MAPK directly inhibits LPS-induced IL-6 production from RPMI-8226 cell (IC50=100 pM). Emprumapimod can be used for the research of dilated cardiomyopathy and acute inflammatory pain[1][2].

Name Emprumapimod
Description Emprumapimod is a potent, orally bioavailable and selective inhibitor of p38α MAPK directly inhibits LPS-induced IL-6 production from RPMI-8226 cell (IC50=100 pM). Emprumapimod can be used for the research of dilated cardiomyopathy and acute inflammatory pain[1][2].
Related Catalog
Target

p38α:100 pM (IC50)

In Vivo In SCID-beige mice, LPS (3 μg/kg) induced IL-6 (7897±827 pg/mL) and TNF-α (1922±282 pg/mL) after 2 hours and these cytokines are inhibited by oral administration of Emprumapimod (ARRY-797; 30 mg/kg) by 91% and 95%, respectively[1]. In MM xenograft models, Emprumapimod (30 mg/kg, BID, PO) inhibits RPMI 8226 tumor growth by 72% as a single agent and by 56% when LPS is administered to stimulate growth in vivo[1]. Emprumapimod also inhibits LPS-induced phosphorylation of p38 in RPMI-8226 xenografts[1]. Treatment of LmnaH222P/H222P mice with the p38α inhibitor Emprumapimod (ARRY-371797; 30 mg/kg; orally twice daily; for 4 weeks initiated at 16 weeks of age) prevents left ventricular (LV) dilatation and deterioration of fractional shortening (FS). LV end-diastolic diameter (LVEDD) and LV end-systolic diameter (LVESD) in LmnaH222P/H222P mice treated with Emprumapimod are significantly smaller and FS is significantly increased compared with the placebo-treated mice[2]. Animal Model: LmnaH222P/H222P mice were[2] Dosage: 30 mg/kg Administration: Administered orally by gavage starting when mice were 16 weeks of age and continuing until 20 weeks of age Result: There were significant increases in LVEDD and LVESD as well as a decrease in FS, a parameter directly proportional to the LV ejection fraction.
References

[1]. Dale Wright, et al. ARRY-797, a Potent and Selective Inhibitor of p38 Map Kinase, Inhibits LPS-Induced IL-6 and In Vivo Growth of RPMI-8226 Human Multiple Myeloma Cells.

[2]. Antoine Muchir, et al. Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation. Hum Mol Genet. 2012 Oct 1;21(19):4325-33.

Molecular Formula C24H29F2N5O3
Molecular Weight 473.52
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.