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SNX-2112 5mg  | Purity Not Available

Selleck Chemicals

SNX-2112 selectively binds to the ATP pocket of HSP90α and HSP90β with Ka of 30 nM and 30 nM, uniformly more potent than 17-AAG.

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SNX-2112 50mg  | Purity Not Available

Selleck Chemicals

SNX-2112 selectively binds to the ATP pocket of HSP90α and HSP90β with Ka of 30 nM and 30 nM, uniformly more potent than 17-AAG.

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SNX-2112 10mM/1mL  | Purity Not Available

Selleck Chemicals

SNX-2112 selectively binds to the ATP pocket of HSP90α and HSP90β with Ka of 30 nM and 30 nM, uniformly more potent than 17-AAG.

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PF-04929113 (SNX-5422) 5mg  | Purity Not Available

Selleck Chemicals

PF-04929113 (SNX-5422) is a potent and selective HSP90 inhibitor with Kd of 41 nM and induces Her-2 degradation with IC50 of 37 nM. Phase 1/2.

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GW3965 HCl 5mg  | Purity Not Available

Selleck Chemicals

GW3965 HCl is a potent, selective LXR agonist for hLXRα and hLXRβ with EC50 of 190 and 30 nM in cell-free assays, respectively.

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GW3965 HCl 50mg  | Purity Not Available

Selleck Chemicals

GW3965 HCl is a potent, selective LXR agonist for hLXRα and hLXRβ with EC50 of 190 and 30 nM in cell-free assays, respectively.

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GW3965 HCl 10mM/1mL  | Purity Not Available

Selleck Chemicals

GW3965 HCl is a potent, selective LXR agonist for hLXRα and hLXRβ with EC50 of 190 and 30 nM in cell-free assays, respectively.

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URB597 25mg  | Purity Not Available

Selleck Chemicals

URB597 (KDS-4103) is a potent, orally bioavailable FAAH inhibitor with IC50 of 4.6 nM, with no activity on other cannabinoid-related targets. Phase 1.

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BMS-378806 5mg  | Purity Not Available

Selleck Chemicals

BMS-378806 (BMS 806) selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.

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BMS-378806 50mg  | Purity Not Available

Selleck Chemicals

BMS-378806 (BMS 806) selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.

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