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Cayman Chemical

Our mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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VUF 5574 5 mg | ≥98%

Cayman Chemical

An adenosine A3 receptor antagonist

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VUF 5574 1 mg | ≥98%

Cayman Chemical

An adenosine A3 receptor antagonist

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VUF10460 25 mg | ≥98%

Cayman Chemical

A histamine H4 receptor agonist

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VUF10460 10 mg | ≥98%

Cayman Chemical

A histamine H4 receptor agonist

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VUF10460 5 mg | ≥98%

Cayman Chemical

A histamine H4 receptor agonist

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VUF10460 1 mg | ≥98%

Cayman Chemical

A histamine H4 receptor agonist

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VUF8430 (hydrobromide) 25 mg | ≥95%

Cayman Chemical

A histamine H4 receptor agonist

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VUF8430 (hydrobromide) 10 mg | ≥95%

Cayman Chemical

A histamine H4 receptor agonist

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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 p38a MAPK inhibitor

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VX-745 10 mg | ≥95%

Cayman Chemical

A p38a MAPK inhibitor

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VX-745 5 mg | ≥95%

Cayman Chemical

A p38a 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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VX-984 1 mg | ≥95%

Cayman Chemical

An inhibitor of DNA-PK

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VX-984 10 mg | ≥95%

Cayman Chemical

An inhibitor of DNA-PK

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VX-984 5 mg | ≥95%

Cayman Chemical

An inhibitor of DNA-PK

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VZ 185 1 mg | ≥98%

Cayman Chemical

A PROTAC that drives BRD7 and BRD9 degradation

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VZ 185 10 mg | ≥98%

Cayman Chemical

A PROTAC that drives BRD7 and BRD9 degradation

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VZ 185 5 mg | ≥98%

Cayman Chemical

A PROTAC that drives BRD7 and BRD9 degradation

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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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