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GNE 9605 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
GNE 9605 10mg 10mg | Purity Not Available
Adooq Bioscience
BMS 626529 5mg 5mg | Purity Not Available
Adooq Bioscience
BMS-626529 is a potent HIV-1 attachment inhibitor. BMS-663068 is also the phosphonooxymethyl prodrug of BMS-626529 that targets HIV-1 gp120 and prevents its binding to CD4(+) T cells.
More Information Supplier PageBMS 626529 25mg 25mg | Purity Not Available
Adooq Bioscience
BMS-626529 is a potent HIV-1 attachment inhibitor. BMS-663068 is also the phosphonooxymethyl prodrug of BMS-626529 that targets HIV-1 gp120 and prevents its binding to CD4(+) T cells.
More Information Supplier PageBMS 626529 10mg 10mg | Purity Not Available
Adooq Bioscience
BMS-626529 is a potent HIV-1 attachment inhibitor. BMS-663068 is also the phosphonooxymethyl prodrug of BMS-626529 that targets HIV-1 gp120 and prevents its binding to CD4(+) T cells.
More Information Supplier PagePRT 062070 50mg 50mg | Purity Not Available
Adooq Bioscience
PRT062070 is a novel, oral, dual spleen tyrosine kinase (Syk) and janus kinase (JAK) inhibitor. Cerdulatinib preferentially inhibited JAK1 and JAK3 dependent cytokine mediated signaling and functional responses in various cell types.
More Information Supplier PagePRT 062070 25mg 25mg | Purity Not Available
Adooq Bioscience
PRT062070 is a novel, oral, dual spleen tyrosine kinase (Syk) and janus kinase (JAK) inhibitor. Cerdulatinib preferentially inhibited JAK1 and JAK3 dependent cytokine mediated signaling and functional responses in various cell types.
More Information Supplier PagePRT 062070 10mg 10mg | Purity Not Available
Adooq Bioscience
PRT062070 is a novel, oral, dual spleen tyrosine kinase (Syk) and janus kinase (JAK) inhibitor. Cerdulatinib preferentially inhibited JAK1 and JAK3 dependent cytokine mediated signaling and functional responses in various cell types.
More Information Supplier PageTH 237A 25mg 25mg | Purity Not Available
Adooq Bioscience
TH-237A is a novel neuroprotective agent, which possess protective properties against ??-amyloid (A??)-induced neurodegeneration associated with Alzheimer’s disease.
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