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Cayman Chemical

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VUF8430 (hydrobromide) 5 mg | ≥95%

Cayman Chemical

A histamine H4 receptor agonist

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VUF8430 (hydrobromide) 1 mg | ≥95%

Cayman Chemical

A histamine H4 receptor agonist

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Vulpinic Acid 25 mg | ≥98%

Cayman Chemical

A lichen metabolite with diverse biological activities

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Vulpinic Acid 100 mg | ≥98%

Cayman Chemical

A lichen metabolite with diverse biological activities

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Vulpinic Acid 50 mg | ≥98%

Cayman Chemical

A lichen metabolite with diverse biological activities

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Vulpinic Acid 10 mg | ≥98%

Cayman Chemical

A lichen metabolite with diverse biological activities

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VV116 1 mg | ≥95%

Cayman Chemical

An antiviral agent and a derivative of remdesivir

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VV116 5 mg | ≥95%

Cayman Chemical

An antiviral agent and a derivative of remdesivir

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VV116 10 mg | ≥95%

Cayman Chemical

An antiviral agent and a derivative of remdesivir

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VV116 25 mg | ≥95%

Cayman Chemical

An antiviral agent and a derivative of remdesivir

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VX-509 25 mg | ≥98%

Cayman Chemical

A selective JAK3 inhibitor

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VX-509 10 mg | ≥98%

Cayman Chemical

A selective JAK3 inhibitor

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VX-509 5 mg | ≥98%

Cayman Chemical

A selective JAK3 inhibitor

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VX-509 1 mg | ≥98%

Cayman Chemical

A selective JAK3 inhibitor

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VX-702 25 mg | ≥95%

Cayman Chemical

An inhibitor of p38 MAP kinases

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VX-702 10 mg | ≥95%

Cayman Chemical

An inhibitor of p38 MAP kinases

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VX-702 5 mg | ≥95%

Cayman Chemical

An inhibitor of p38 MAP kinases

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VX-745 50 mg | ≥95%

Cayman Chemical

A p38α MAPK inhibitor

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VX-745 10 mg | ≥95%

Cayman Chemical

A p38α MAPK inhibitor

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VX-745 5 mg | ≥95%

Cayman Chemical

A p38α MAPK inhibitor

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VX-745 1 mg | ≥95%

Cayman Chemical

A p38α MAPK inhibitor

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VX-765 50 mg | ≥98%

Cayman Chemical

A prodrug form of VRT-043198

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VX-765 25 mg | ≥98%

Cayman Chemical

A prodrug form of VRT-043198

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VX-765 10 mg | ≥98%

Cayman Chemical

A prodrug form of VRT-043198

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VX-765 5 mg | ≥98%

Cayman Chemical

A prodrug form of VRT-043198

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VX-809 25 mg | ≥98%

Cayman Chemical

A F508del-CFTR corrector

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VX-809 10 mg | ≥98%

Cayman Chemical

A F508del-CFTR corrector

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VX-809 5 mg | ≥98%

Cayman Chemical

A F508del-CFTR corrector

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VX-809 1 mg | ≥98%

Cayman Chemical

A F508del-CFTR corrector

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W-13 (hydrochloride) 10 mg | ≥98%

Cayman Chemical

A potent calmodulin antagonist

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W-13 (hydrochloride) 5 mg | ≥98%

Cayman Chemical

A potent calmodulin antagonist

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W-13 (hydrochloride) 1 mg | ≥98%

Cayman Chemical

A potent calmodulin antagonist

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W-5 (hydrochloride) 25 mg | ≥98%

Cayman Chemical

A low-affinity calmodulin antagonist

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W-5 (hydrochloride) 5 mg | ≥98%

Cayman Chemical

A low-affinity calmodulin antagonist

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W-54011 25 mg | ≥98%

Cayman Chemical

A selective C5aR antagonist

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W-54011 10 mg | ≥98%

Cayman Chemical

A selective C5aR antagonist

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W-54011 5 mg | ≥98%

Cayman Chemical

A selective C5aR antagonist

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W-54011 1 mg | ≥98%

Cayman Chemical

A selective C5aR antagonist

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W-7 (hydrochloride) 100 mg | ≥98%

Cayman Chemical

A cell-permeable antagonist of calmodulin

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W-7 (hydrochloride) 50 mg | ≥98%

Cayman Chemical

A cell-permeable antagonist of calmodulin

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W-7 (hydrochloride) 10 mg | ≥98%

Cayman Chemical

A cell-permeable antagonist of calmodulin

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W123 10 mg | ≥98%

Cayman Chemical

Antagonist of spingosine 1-phosphate type 1 receptor

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W123 5 mg | ≥98%

Cayman Chemical

Antagonist of spingosine 1-phosphate type 1 receptor

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W123 1 mg | ≥98%

Cayman Chemical

Antagonist of spingosine 1-phosphate type 1 receptor

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W140 (trifluoroacetate salt) 10 mg | ≥95%

Cayman Chemical

An inactive enantiomer of W146

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W140 (trifluoroacetate salt) 5 mg | ≥95%

Cayman Chemical

An inactive enantiomer of W146

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W140 (trifluoroacetate salt) 1 mg | ≥95%

Cayman Chemical

An inactive enantiomer of W146

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W140 (trifluoroacetate salt) 500 µg | ≥95%

Cayman Chemical

An inactive enantiomer of W146

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W146 (trifluoroacetate salt) 10 mg | ≥95%

Cayman Chemical

An S1P1 receptor antagonist

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W146 (trifluoroacetate salt) 5 mg | ≥95%

Cayman Chemical

An S1P1 receptor antagonist

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