M 344 |
An inhibitor of HDACs, inhibiting maize HDAC (IC50 = 100 nM) as well as hu… |
5 mg |
13174-5 |
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M 344 |
An inhibitor of HDACs, inhibiting maize HDAC (IC50 = 100 nM) as well as hu… |
50 mg |
13174-50 |
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M04 |
A STING agonist; induces IFN reporter gene expression in HEK293T cells exp… |
1 mg |
35454-1 |
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M04 |
A STING agonist; induces IFN reporter gene expression in HEK293T cells exp… |
500 µg |
35454-500 |
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M1001 |
A modulator of HIF-2α; stabilizes the ARNT and HIF-2α protein-… |
1 mg |
37393-1 |
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M1001 |
A modulator of HIF-2α; stabilizes the ARNT and HIF-2α protein-… |
10 mg |
37393-10 |
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M1001 |
A modulator of HIF-2α; stabilizes the ARNT and HIF-2α protein-… |
25 mg |
37393-25 |
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M1001 |
A modulator of HIF-2α; stabilizes the ARNT and HIF-2α protein-… |
5 mg |
37393-5 |
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M-144 |
Differs from UR-144 by having a fluorine atom on the terminal carbon of th… |
1 mg |
16084-1 |
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M-144 |
Differs from UR-144 by having a fluorine atom on the terminal carbon of th… |
10 mg |
16084-10 |
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M-144 |
Differs from UR-144 by having a fluorine atom on the terminal carbon of th… |
5 mg |
16084-5 |
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M2698 |
A dual inhibitor of p70S6K and Akt1 (IC50s = 1.1 and 4 nM, respectively);… |
1 mg |
36816-1 |
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M2698 |
A dual inhibitor of p70S6K and Akt1 (IC50s = 1.1 and 4 nM, respectively);… |
10 mg |
36816-10 |
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M2698 |
A dual inhibitor of p70S6K and Akt1 (IC50s = 1.1 and 4 nM, respectively);… |
25 mg |
36816-25 |
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M2698 |
A dual inhibitor of p70S6K and Akt1 (IC50s = 1.1 and 4 nM, respectively);… |
5 mg |
36816-5 |
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M-3258 |
An LMP7 inhibitor (IC50 = 4.1 nM); selective over the 20S proteasomal cata… |
1 mg |
38160-1 |
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M-3258 |
An LMP7 inhibitor (IC50 = 4.1 nM); selective over the 20S proteasomal cata… |
10 mg |
38160-10 |
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M-3258 |
An LMP7 inhibitor (IC50 = 4.1 nM); selective over the 20S proteasomal cata… |
5 mg |
38160-5 |
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M50054 |
A cell-permeable inhibitor of caspase-3 activation; blocks apoptosis in a… |
1 mg |
20810-1 |
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M50054 |
A cell-permeable inhibitor of caspase-3 activation; blocks apoptosis in a… |
10 mg |
20810-10 |
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M50054 |
A cell-permeable inhibitor of caspase-3 activation; blocks apoptosis in a… |
25 mg |
20810-25 |
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M50054 |
A cell-permeable inhibitor of caspase-3 activation; blocks apoptosis in a… |
5 mg |
20810-5 |
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MA-0204 |
An agonist of PPARδ; selectively induces reporter gene expression in… |
1 mg |
26025-1 |
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MA-0204 |
An agonist of PPARδ; selectively induces reporter gene expression in… |
10 mg |
26025-10 |
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MA-0204 |
An agonist of PPARδ; selectively induces reporter gene expression in… |
5 mg |
26025-5 |
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Maackiain |
the histamine H1 receptor in serum-starved HeLa cells at 10, 20, or 30 &mi… |
1 mg |
40215-1 |
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Maackiain |
the histamine H1 receptor in serum-starved HeLa cells at 10, 20, or 30 &mi… |
10 mg |
40215-10 |
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Maackiain |
the histamine H1 receptor in serum-starved HeLa cells at 10, 20, or 30 &mi… |
25 mg |
40215-25 |
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Maackiain |
the histamine H1 receptor in serum-starved HeLa cells at 10, 20, or 30 &mi… |
5 mg |
40215-5 |
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Mabuterol |
A β2-adrenergic receptor agonist; induces relaxation of isolated trac… |
1 mg |
23246-1 |
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Mabuterol |
A β2-adrenergic receptor agonist; induces relaxation of isolated trac… |
10 mg |
23246-10 |
More Info
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Mabuterol |
A β2-adrenergic receptor agonist; induces relaxation of isolated trac… |
5 mg |
23246-5 |
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Macbecin I |
An Hsp90 inhibitor (IC50 = 2 mM for Hsp90 ATPase activity); inhibits growt… |
1 mg |
22225-1 |
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MA-CHMINACA |
An analog of AB-CHMINACA metabolite M2 in which the hydroxyl moiety is rep… |
1 mg |
16421-1 |
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MA-CHMINACA |
An analog of AB-CHMINACA metabolite M2 in which the hydroxyl moiety is rep… |
10 mg |
16421-10 |
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MA-CHMINACA |
An analog of AB-CHMINACA metabolite M2 in which the hydroxyl moiety is rep… |
5 mg |
16421-5 |
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Macitentan |
A dual ETA / ETB receptor antagonist (IC50s = 0.5 and 391 nM in a radiolig… |
100 mg |
23304-100 |
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Macitentan |
A dual ETA / ETB receptor antagonist (IC50s = 0.5 and 391 nM in a radiolig… |
25 mg |
23304-25 |
More Info
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Macitentan |
A dual ETA / ETB receptor antagonist (IC50s = 0.5 and 391 nM in a radiolig… |
250 mg |
23304-250 |
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Macitentan |
A dual ETA / ETB receptor antagonist (IC50s = 0.5 and 391 nM in a radiolig… |
50 mg |
23304-50 |
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Macitentan-d4 |
An internal standard for the quantification of macitentan by GC- or LC-MS |
1 mg |
28522-1 |
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Macranthoidin B |
A triterpenoid saponin with anticancer activity; increases the production… |
1 mg |
31533-1 |
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Macranthoidin B |
A triterpenoid saponin with anticancer activity; increases the production… |
10 mg |
31533-10 |
More Info
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Macranthoidin B |
A triterpenoid saponin with anticancer activity; increases the production… |
25 mg |
31533-25 |
More Info
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Macranthoidin B |
A triterpenoid saponin with anticancer activity; increases the production… |
5 mg |
31533-5 |
More Info
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Macrophage (mouse) Elicitation Kit |
Macrophages are long-lived tissue resident cells that function to ingest a… |
1 ea |
601740-1EA |
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(+)-Macrosphelide A |
A fungal metabolite; inhibits adhesion of HL-60 human leukemia cells to HU… |
1 mg |
27704-1 |
More Info
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(+)-Macrosphelide A |
A fungal metabolite; inhibits adhesion of HL-60 human leukemia cells to HU… |
5 mg |
27704-5 |
More Info
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(+)-Macrosphelide A |
A fungal metabolite; inhibits adhesion of HL-60 human leukemia cells to HU… |
500 µg |
27704-500 |
More Info
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Maculosin |
A diketopiperazine metabolite; induces formation of weeping necrotic lesio… |
25 mg |
25019-25 |
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