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D355716-1mg16,16-dimethyl Prostaglandin A1 is a metabolism resistant analog of PGA1 that inhibits the viral replication in both HSV and HIV-1 infection systems|in vitro|at concentrations that do not adversely alter cellular DNA synthesis. The ID|50|values for
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D355716-5mg16,16-dimethyl Prostaglandin A1 is a metabolism resistant analog of PGA1 that inhibits the viral replication in both HSV and HIV-1 infection systems|in vitro|at concentrations that do not adversely alter cellular DNA synthesis. The ID|50|values for
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D338904-1mg16,16-dimethyl Prostaglandin A2 is a metabolism resistant analog of PGA2 with a relatively prolonged half-life. This compound has been shown to inhibit the proliferation of Sendai virus in cultured African green monkey kidney cells by >:90% at a
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D338904-5mg16,16-dimethyl Prostaglandin A2 is a metabolism resistant analog of PGA2 with a relatively prolonged half-life. This compound has been shown to inhibit the proliferation of Sendai virus in cultured African green monkey kidney cells by >:90% at a
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H329631-1mg17-Hydroxyventuricidin A has antibacterial activity against gram-positive bacteria.
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H329631-250μg17-Hydroxyventuricidin A has antibacterial activity against gram-positive bacteria.
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H340930-1mg17β-hydroxy Wortmannin is an analog of wortmannin . It irreversibly binds PI 3-kinase and potently blocks fMLP-stimulated respiratory burst in neutrophils (IC|50|= 5 nM). 17β-hydroxy Wortmannin inhibits recombinant PI 3-kinase and mTOR (IC|50|= 2.7
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H340930-500μg17β-hydroxy Wortmannin is an analog of wortmannin . It irreversibly binds PI 3-kinase and potently blocks fMLP-stimulated respiratory burst in neutrophils (IC|50|= 5 nM). 17β-hydroxy Wortmannin inhibits recombinant PI 3-kinase and mTOR (IC|50|= 2.7
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C169986-25mg2′-C-Methylguanosine.
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C169986-5mg2′-C-Methylguanosine.
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C341839-1g2'-Chloro-2'-deoxycytidine is a nucleoside derivative.
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C341839-5g2'-Chloro-2'-deoxycytidine is a nucleoside derivative.