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58698 results for "Cayman Chemical"

58698 Results for: "Cayman Chemical"

Baccatin III 1 * 50 mg

Supplier: Cayman Chemical

Baccatin III 1 * 50 mg

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TAS 120 1 * 10 mg

Supplier: Cayman Chemical

TAS 120 1 * 10 mg

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SR 59230A (hydrochloride) 1 * 10 mg

Supplier: Cayman Chemical

SR 59230A (hydrochloride) 1 * 10 mg

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AZD 2014 1 * 10 mg

Supplier: Cayman Chemical

AZD 2014 1 * 10 mg

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3-(4-Chlorophenyl)-4-hydroxybutyric Acid (sodium salt) 1 * 500 µG

Supplier: Cayman Chemical

3-(4-Chlorophenyl)-4-hydroxybutyric Acid (sodium salt) 1 * 500 µG

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WEHI-539 1 * 1 mg

Supplier: Cayman Chemical

WEHI-539 1 * 1 mg

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Temozolomide-d3 1 * 500 µG

Supplier: Cayman Chemical

Temozolomide-d3 1 * 500 µG

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SSR 69071 1 * 5 mg

Supplier: Cayman Chemical

SSR 69071 1 * 5 mg

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INH6 1 * 1 mg

Supplier: Cayman Chemical

INH6 1 * 1 mg

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CGS 15943 1 * 5 mg

Supplier: Cayman Chemical

CGS 15943 1 * 5 mg

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Leptomycin A 1 * 100 µG

Supplier: Cayman Chemical

Leptomycin A 1 * 100 µG

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CPCCOEt 1 * 10 mg

Supplier: Cayman Chemical

CPCCOEt 1 * 10 mg

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CP 547,632 1 * 5 mg

Supplier: Cayman Chemical

CP 547,632 1 * 5 mg

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Astragaloside I 1 * 5 mg

Supplier: Cayman Chemical

Astragaloside I 1 * 5 mg

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R428 1 * 5 mg

Supplier: Cayman Chemical

R428 1 * 5 mg

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An inhibitor of UCH-L1 activity (IC50 = 0.88 Ki = 0.4 M) that demonstrates selectivity for UCH-L1 compared to UCH-L3 (IC50 = 25 M) 1 * 5 mg

Supplier: Cayman Chemical

An inhibitor of UCH-L1 activity (IC50 = 0.88 Ki = 0.4 M) that demonstrates selectivity for UCH-L1 compared to UCH-L3 (IC50 = 25 M) 1 * 5 mg

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LYS6K2 1 * 25 mg

Supplier: Cayman Chemical

LYS6K2 1 * 25 mg

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An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 M) 1 * 1 mg

Supplier: Cayman Chemical

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 M) 1 * 1 mg

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An analog of geldanamycin which has potent in vivo activity and reduced toxicity 1 * 10 mg

Supplier: Cayman Chemical

An analog of geldanamycin which has potent in vivo activity and reduced toxicity 1 * 10 mg

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A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s = 6 and 15 nM, respectively) and G9a/GLP-mediated dimethy lation of histone 3 on lysine 9 in MDA-MB-231 cells (IC50 = 26 nM) 1 * 1 mg

Supplier: Cayman Chemical

A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s = 6 and 15 nM, respectively) and G9a/GLP-mediated dimethy lation of histone 3 on lysine 9 in MDA-MB-231 cells (IC50 = 26 nM) 1 * 1 mg

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N-(2-HYDROXYETHYL)-NAPHTHALIMIDE 1 * 1 g

Supplier: Cayman Chemical

N-(2-HYDROXYETHYL)-NAPHTHALIMIDE 1 * 1 g

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UNC2250 1 * 10 mg

Supplier: Cayman Chemical

UNC2250 1 * 10 mg

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YS-035 (HYDROCHLORIDE) 1 * 10 mg

Supplier: Cayman Chemical

YS-035 (HYDROCHLORIDE) 1 * 10 mg

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TAK-960 1 * 1 mg

Supplier: Cayman Chemical

TAK-960 1 * 1 mg

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(E)-2-HEXADECENAL 1 * 5 mg

Supplier: Cayman Chemical

(E)-2-HEXADECENAL 1 * 5 mg

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ADENOSINE KINASE INHIBITOR (HYDRATE) 1 * 5 mg

Supplier: Cayman Chemical

ADENOSINE KINASE INHIBITOR (HYDRATE) 1 * 5 mg

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ZOXAZOLAMINE 1 * 1 g

Supplier: Cayman Chemical

ZOXAZOLAMINE 1 * 1 g

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A potent, dual PI3K/mTOR inhibitor (IC50 values are 0.4 and 5.4 nM for PI3K and PI3K, respectively, and 1.6 nM for mTOR) 1 * 10 mg

Supplier: Cayman Chemical

A potent, dual PI3K/mTOR inhibitor (IC50 values are 0.4 and 5.4 nM for PI3K and PI3K, respectively, and 1.6 nM for mTOR) 1 * 10 mg

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A dual agonist of PPARα and γ (IC50s = 1 and 0.2 µM, respectively) that at 3 µM/kg/day for 3 weeks has been used to reduce insulin r esistance in obese Zucker rats 1 * 50 mg

Supplier: Cayman Chemical

A dual agonist of PPARα and γ (IC50s = 1 and 0.2 µM, respectively) that at 3 µM/kg/day for 3 weeks has been used to reduce insulin r esistance in obese Zucker rats 1 * 50 mg

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MINOXIDIL-D10 1 * 500 µG

Supplier: Cayman Chemical

MINOXIDIL-D10 1 * 500 µG

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