Description
H7 is an inhibitor of PKC and PKG that is used to study the effects of protein kinase signaling in research models.
H7 is an inhibitor of PKC and PKG that is used to study the effects of protein kinase signaling in research models.
| Cas No. | 108930-17-2 |
|---|---|
| Purity | ≥98% |
| Formula | C14H17N3O2S • 2HCl |
| Formula Wt. | 364.30 |
| IUPAC Name | 5-(2-methylpiperazin-1-yl)sulfonylisoquinoline;dihydrochloride |
| Synonym | (-)-1-(5-Isoquinolinesulfonyl)-2-methylpiperazine di-HCl salt |
| Melting Point | 215-225°C |
| Solubility | Soluble in water. |
| Store Temp | 4°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Chen JJ, Zhang J, Cai Y, et al. C-type natriuretic peptide inhibiting vascular calcification might involve decreasing bone morphogenic protein 2 and osteopontin levels. Mol Cell Biochem. 2014 Jul;392(1-2):65-76. PMID: 24710639.
Zhang Y, Bao S, Kuang Z, et al. Urotensin II promotes monocyte chemoattractant protein-1 expression in aortic adventitial fibroblasts of rat. Chin Med J (Engl). 2014 May;127(10):1907-12. PMID: 24824254.
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