U-74389G |
U-74389G is an antioxidant which prevents iron-dependent lipid peroxidatio… |
250 mg |
75860-250 |
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U-74389G |
U-74389G is an antioxidant which prevents iron-dependent lipid peroxidatio… |
50 mg |
75860-50 |
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U-46619 Glycine methyl ester |
An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… |
100 µg |
10010522-100 |
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U-46619 Glycine methyl ester |
An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… |
25 µg |
10010522-25 |
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U-46619 Glycine methyl ester |
An analog of U-46619, a stable analog of the endoperoxide PGH2 in the arac… |
50 µg |
10010522-50 |
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UGT8 Inhibitor 19 |
An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… |
1 mg |
32723-1 |
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UGT8 Inhibitor 19 |
An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… |
10 mg |
32723-10 |
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UGT8 Inhibitor 19 |
An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… |
25 mg |
32723-25 |
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UGT8 Inhibitor 19 |
An inhibitor of UGT8 (IC50 = 0.2 nM); selective for UGT8 over UGT1A1, -1A6… |
5 mg |
32723-5 |
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UHRF1 PHD domain (human recombinant) |
Source: Recombinant N-terminal GST-tagged protein expressed in E. coli &bu… |
100 µg |
14777-100 |
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UHRF1 tudor-like region (human recombinant; His-tagged) |
Source: Recombinant protein expressed in E. coli • MW: 31.9 kDa |
100 µg |
14779-100 |
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UK 1 |
A cytotoxic Streptomyces metabolite that inhibits topoisomerase II and hep… |
1 mg |
20139-1 |
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UK 1 |
A cytotoxic Streptomyces metabolite that inhibits topoisomerase II and hep… |
5 mg |
20139-5 |
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UK 356618 |
An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… |
10 mg |
32859-10 |
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UK 356618 |
An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… |
25 mg |
32859-25 |
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UK 356618 |
An MMP-3 inhibitor (IC50 = 5.9 nM); selective for MMP-3 over MMP-1, -2, -9… |
5 mg |
32859-5 |
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UK 371804 |
A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… |
10 mg |
27225-10 |
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UK 371804 |
A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… |
25 mg |
27225-25 |
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UK 371804 |
A uPA inhibitor (Ki = 10 nM); 4,000- and 2,700-fold selective for uPA over… |
5 mg |
27225-5 |
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UK 383367 |
A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… |
1 mg |
15029-1 |
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UK 383367 |
A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… |
10 mg |
15029-10 |
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UK 383367 |
A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… |
25 mg |
15029-25 |
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UK 383367 |
A potent, selective inhibitor of BMP1 (IC50 = 44 nM); effective in a cell-… |
5 mg |
15029-5 |
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UK 5099 |
An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… |
1 mg |
16980-1 |
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UK 5099 |
An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… |
10 mg |
16980-10 |
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UK 5099 |
An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… |
25 mg |
16980-25 |
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UK 5099 |
An inhibitor of the mitochondrial pyruvate carrier; inhibits pyruvate-depe… |
5 mg |
16980-5 |
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UK 122 (trifluoroacetate salt) |
A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… |
1 mg |
9001218-1 |
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UK 122 (trifluoroacetate salt) |
A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… |
10 mg |
9001218-10 |
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UK 122 (trifluoroacetate salt) |
A uPA inhibitor (IC50 = 0.2 µM); selective for uPA over tPA, trypsin… |
5 mg |
9001218-5 |
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Ulipristal Acetate |
A selective progesterone receptor modulator (SPRM) that binds to human PR-… |
10 mg |
23657-10 |
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Ulipristal Acetate |
A selective progesterone receptor modulator (SPRM) that binds to human PR-… |
25 mg |
23657-25 |
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Ulipristal Acetate |
A selective progesterone receptor modulator (SPRM) that binds to human PR-… |
5 mg |
23657-5 |
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Ulipristal Acetate |
A selective progesterone receptor modulator (SPRM) that binds to human PR-… |
50 mg |
23657-50 |
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Ulipristal Acetate-d6 |
An internal standard for the quantification of ulipristal acetate by GC- o… |
1 mg |
26446-1 |
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Ulixertinib (hydrochloride) |
A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM |
1 mg |
18298-1 |
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Ulixertinib (hydrochloride) |
A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM |
10 mg |
18298-10 |
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Ulixertinib (hydrochloride) |
A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM |
25 mg |
18298-25 |
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Ulixertinib (hydrochloride) |
A reversible ERK1 / 2 inhibitor (IC50 50 value of 180 nM |
5 mg |
18298-5 |
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ULK-101 |
A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… |
1 mg |
40403-1 |
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ULK-101 |
A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… |
10 mg |
40403-10 |
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ULK-101 |
A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… |
25 mg |
40403-25 |
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ULK-101 |
A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… |
5 mg |
40403-5 |
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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 |
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UltraPure Water |
Water used for the preparation of ELISA reagents and buffers |
1 L |
400000-1 |
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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 |
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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 |
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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 |
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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 |
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U-99194 (maleate) |
A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… |
10 mg |
35854-10 |
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U-99194 (maleate) |
A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… |
25 mg |
35854-25 |
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U-99194 (maleate) |
A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… |
5 mg |
35854-5 |
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U-99194 (maleate) |
A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… |
50 mg |
35854-50 |
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UMB-32 |
An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… |
1 mg |
17123-1 |
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UMB-32 |
An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… |
10 mg |
17123-10 |
More Info
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UMB-32 |
An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… |
25 mg |
17123-25 |
More Info
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UMB-32 |
An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… |
5 mg |
17123-5 |
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Umbelliferone |
A derivative and metabolite of coumarin with diverse biological activities… |
100 mg |
24665-100 |
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Umbelliferone |
A derivative and metabolite of coumarin with diverse biological activities… |
25 mg |
24665-25 |
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Umbelliferone |
A derivative and metabolite of coumarin with diverse biological activities… |
50 mg |
24665-50 |
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Umbelliprenin |
A prenylated coumarin with diverse biological activities; inhibits 5-LO in… |
1 mg |
27894-1 |
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Umbelliprenin |
A prenylated coumarin with diverse biological activities; inhibits 5-LO in… |
10 mg |
27894-10 |
More Info
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Umbelliprenin |
A prenylated coumarin with diverse biological activities; inhibits 5-LO in… |
25 mg |
27894-25 |
More Info
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Umbelliprenin |
A prenylated coumarin with diverse biological activities; inhibits 5-LO in… |
5 mg |
27894-5 |
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Umeclidinium (bromide) |
A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… |
10 mg |
20700-10 |
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Umeclidinium (bromide) |
A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… |
100 mg |
20700-100 |
More Info
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Umeclidinium (bromide) |
A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… |
50 mg |
20700-50 |
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U-62066 (mesylate) |
An analytical reference standard categorized as an opioid; intended for re… |
1 mg |
25072-1 |
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U-62066 (mesylate) |
An analytical reference standard categorized as an opioid; intended for re… |
5 mg |
25072-5 |
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UMI-77 |
A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… |
1 mg |
19148-1 |
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UMI-77 |
A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… |
10 mg |
19148-10 |
More Info
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UMI-77 |
A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… |
5 mg |
19148-5 |
More Info
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Umifenovir-d6 (hydrochloride) |
An internal standard for the quantification of arbidol by GC- or LC-MS |
1 mg |
31494-1 |
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Umifenovir-d6 (hydrochloride) |
An internal standard for the quantification of arbidol by GC- or LC-MS |
5 mg |
31494-5 |
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Umifenovir-d6 (hydrochloride) |
An internal standard for the quantification of arbidol by GC- or LC-MS |
500 µg |
31494-500 |
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