CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 835 of 870
Non-Antibody Products
Page 835 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| U-74389G | U-74389G is an antioxidant which prevents iron-dependent lipid peroxidatio… | 250 mg | 75860-250 | More Info |
| U-74389G | U-74389G is an antioxidant which prevents iron-dependent lipid peroxidatio… | 50 mg | 75860-50 | More Info |
| U-46619 Glycine methyl ester | An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… | 100 µg | 10010522-100 | More Info |
| U-46619 Glycine methyl ester | An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… | 25 µg | 10010522-25 | More Info |
| U-46619 Glycine methyl ester | An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… | 50 µg | 10010522-50 | More Info |
| UGT8 Inhibitor 19 | An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… | 1 mg | 32723-1 | More Info |
| UGT8 Inhibitor 19 | An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… | 10 mg | 32723-10 | More Info |
| UGT8 Inhibitor 19 | An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… | 25 mg | 32723-25 | More Info |
| UGT8 Inhibitor 19 | An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… | 5 mg | 32723-5 | More Info |
| UHRF1 PHD domain (human recombinant) | Source: Recombinant N-terminal GST-tagged protein expressed in E. coli &bu… | 100 µg | 14777-100 | More Info |
| UHRF1 tudor-like region (human recombinant; His-tagged) | Source: Recombinant protein expressed in E. coli • MW: 31.9 kDa | 100 µg | 14779-100 | More Info |
| UK 1 | A cytotoxic Streptomyces metabolite that inhibits topoisomerase II and hep… | 1 mg | 20139-1 | More Info |
| UK 1 | A cytotoxic Streptomyces metabolite that inhibits topoisomerase II and hep… | 5 mg | 20139-5 | More Info |
| UK 356618 | An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… | 10 mg | 32859-10 | More Info |
| UK 356618 | An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… | 25 mg | 32859-25 | More Info |
| UK 356618 | An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… | 5 mg | 32859-5 | More Info |
| UK 371804 | A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… | 10 mg | 27225-10 | More Info |
| UK 371804 | A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… | 25 mg | 27225-25 | More Info |
| UK 371804 | A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… | 5 mg | 27225-5 | More Info |
| UK 383367 | A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… | 1 mg | 15029-1 | More Info |
| UK 383367 | A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… | 10 mg | 15029-10 | More Info |
| UK 383367 | A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… | 25 mg | 15029-25 | More Info |
| UK 383367 | A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… | 5 mg | 15029-5 | More Info |
| UK 5099 | An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… | 1 mg | 16980-1 | More Info |
| UK 5099 | An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… | 10 mg | 16980-10 | More Info |
| UK 5099 | An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… | 25 mg | 16980-25 | More Info |
| UK 5099 | An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… | 5 mg | 16980-5 | More Info |
| UK 122 (trifluoroacetate salt) | A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… | 1 mg | 9001218-1 | More Info |
| UK 122 (trifluoroacetate salt) | A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… | 10 mg | 9001218-10 | More Info |
| UK 122 (trifluoroacetate salt) | A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… | 5 mg | 9001218-5 | More Info |
| Ulipristal Acetate | A selective progesterone receptor modulator (SPRM) that binds to human PR-… | 10 mg | 23657-10 | More Info |
| Ulipristal Acetate | A selective progesterone receptor modulator (SPRM) that binds to human PR-… | 25 mg | 23657-25 | More Info |
| Ulipristal Acetate | A selective progesterone receptor modulator (SPRM) that binds to human PR-… | 5 mg | 23657-5 | More Info |
| Ulipristal Acetate | A selective progesterone receptor modulator (SPRM) that binds to human PR-… | 50 mg | 23657-50 | More Info |
| Ulipristal Acetate-d6 | An internal standard for the quantification of ulipristal acetate by GC- o… | 1 mg | 26446-1 | More Info |
| Ulixertinib (hydrochloride) | A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM | 1 mg | 18298-1 | More Info |
| Ulixertinib (hydrochloride) | A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM | 10 mg | 18298-10 | More Info |
| Ulixertinib (hydrochloride) | A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM | 25 mg | 18298-25 | More Info |
| Ulixertinib (hydrochloride) | A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM | 5 mg | 18298-5 | More Info |
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 1 mg | 40403-1 | More Info |
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 10 mg | 40403-10 | More Info |
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 25 mg | 40403-25 | More Info |
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 5 mg | 40403-5 | More Info |
| UltraPure LPS from Escherichia coli O111:B4 | A form of LPS extracted from wild-type S-form E. coli serotype O111:B4 and… | 1 mg | 28872-1 | More Info |
| UltraPure Water | Water used for the preparation of ELISA reagents and buffers | 1 L | 400000-1 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 1 mg | 26188-1 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 10 mg | 26188-10 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 25 mg | 26188-25 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 5 mg | 26188-5 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 10 mg | 35854-10 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 25 mg | 35854-25 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 5 mg | 35854-5 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 50 mg | 35854-50 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 1 mg | 17123-1 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 10 mg | 17123-10 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 25 mg | 17123-25 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 5 mg | 17123-5 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 100 mg | 24665-100 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 25 mg | 24665-25 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 50 mg | 24665-50 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 1 mg | 27894-1 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 10 mg | 27894-10 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 25 mg | 27894-25 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 5 mg | 27894-5 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 10 mg | 20700-10 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 100 mg | 20700-100 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 50 mg | 20700-50 | More Info |
| U-62066 (mesylate) | An analytical reference standard categorized as an opioid; intended for re… | 1 mg | 25072-1 | More Info |
| U-62066 (mesylate) | An analytical reference standard categorized as an opioid; intended for re… | 5 mg | 25072-5 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 1 mg | 19148-1 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 10 mg | 19148-10 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 5 mg | 19148-5 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 1 mg | 31494-1 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 5 mg | 31494-5 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 500 µg | 31494-500 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com
http://www.caymanchem.com
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