LMW-PTP Inhibitor I (hydrochloride) |
An inhibitor of LMW-PTPA (IC50 = 0.8 µM); selective for LMW-PTPA ove… |
5 mg |
22277-5 |
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L-NAME (hydrochloride) |
A methyl ester prodrug form of the NOS inhibitor L-NNA; exhibits Ki values… |
1000 mg |
80210-1 |
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L-NAME (hydrochloride) |
A methyl ester prodrug form of the NOS inhibitor L-NNA; exhibits Ki values… |
10000 mg |
80210-10 |
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L-NAME (hydrochloride) |
A methyl ester prodrug form of the NOS inhibitor L-NNA; exhibits Ki values… |
5000 mg |
80210-5 |
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L-NAME (hydrochloride) |
A methyl ester prodrug form of the NOS inhibitor L-NNA; exhibits Ki values… |
50000 mg |
80210-50 |
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L-3-n-Butylphthalide |
A phthalide with antiplatelet and neuroprotective activities; inhibits ADP… |
1 mg |
9003759-1 |
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L-3-n-Butylphthalide |
A phthalide with antiplatelet and neuroprotective activities; inhibits ADP… |
10 mg |
9003759-10 |
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L-3-n-Butylphthalide |
A phthalide with antiplatelet and neuroprotective activities; inhibits ADP… |
5 mg |
9003759-5 |
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LN6023 (hydrochloride) |
A CXCR7 agonist; induces β-arrestin recruitment in a reporter assay u… |
1 mg |
40287-1 |
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LN6023 (hydrochloride) |
A CXCR7 agonist; induces β-arrestin recruitment in a reporter assay u… |
10 mg |
40287-10 |
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LN6023 (hydrochloride) |
A CXCR7 agonist; induces β-arrestin recruitment in a reporter assay u… |
5 mg |
40287-5 |
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L-NIL (hydrochloride) |
A relatively selective inhibitor of iNOS, exhibiting IC50 values of 0.4-3.… |
10 mg |
80310-10 |
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L-NIL (hydrochloride) |
A relatively selective inhibitor of iNOS, exhibiting IC50 values of 0.4-3.… |
100 mg |
80310-100 |
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L-NIL (hydrochloride) |
A relatively selective inhibitor of iNOS, exhibiting IC50 values of 0.4-3.… |
50 mg |
80310-50 |
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L-NIO (hydrochloride) |
L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for… |
10 mg |
80320-10 |
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L-NIO (hydrochloride) |
L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for… |
100 mg |
80320-100 |
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L-NIO (hydrochloride) |
L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for… |
5 mg |
80320-5 |
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L-NIO (hydrochloride) |
L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for… |
50 mg |
80320-50 |
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L-NMMA (acetate) |
A non-selective NOS inhibitor (Kis = ~0.18, ~0.4, and ~6 µM for rat… |
100 mg |
10005031-100 |
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L-NMMA (acetate) |
A non-selective NOS inhibitor (Kis = ~0.18, ~0.4, and ~6 µM for rat… |
25 mg |
10005031-25 |
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L-NMMA (acetate) |
A non-selective NOS inhibitor (Kis = ~0.18, ~0.4, and ~6 µM for rat… |
5 mg |
10005031-5 |
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L-NMMA (acetate) |
A non-selective NOS inhibitor (Kis = ~0.18, ~0.4, and ~6 µM for rat… |
50 mg |
10005031-50 |
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L-NMMA (citrate) |
L-NMMA is a relatively non-selective inhibitor of all NOS isoforms. It is… |
10 mg |
80200-10 |
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L-NMMA (citrate) |
L-NMMA is a relatively non-selective inhibitor of all NOS isoforms. It is… |
100 mg |
80200-100 |
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L-NMMA (citrate) |
L-NMMA is a relatively non-selective inhibitor of all NOS isoforms. It is… |
25 mg |
80200-25 |
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L-NMMA (citrate) |
L-NMMA is a relatively non-selective inhibitor of all NOS isoforms. It is… |
50 mg |
80200-50 |
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L-NNA |
L-NNA is an inhibitor of NOS with some selectivity for the neuronal and en… |
1 g |
80220-1 |
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L-NNA |
L-NNA is an inhibitor of NOS with some selectivity for the neuronal and en… |
10 g |
80220-10 |
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L-NNA |
L-NNA is an inhibitor of NOS with some selectivity for the neuronal and en… |
5 g |
80220-5 |
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L-NNA |
L-NNA is an inhibitor of NOS with some selectivity for the neuronal and en… |
50 g |
80220-50 |
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L-Norvaline |
An inhibitor of arginase and p70S6K1; inhibits arginase-mediated urea prod… |
10 g |
34029-10 |
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L-Norvaline |
An inhibitor of arginase and p70S6K1; inhibits arginase-mediated urea prod… |
100 g |
34029-100 |
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L-Norvaline |
An inhibitor of arginase and p70S6K1; inhibits arginase-mediated urea prod… |
25 g |
34029-25 |
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L-Norvaline |
An inhibitor of arginase and p70S6K1; inhibits arginase-mediated urea prod… |
5 g |
34029-5 |
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LNP023 (hydrochloride) |
A CFB inhibitor (IC50 = 10 nM); selective for CFB over a panel of 41 human… |
1 mg |
37291-1 |
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LNP023 (hydrochloride) |
A CFB inhibitor (IC50 = 10 nM); selective for CFB over a panel of 41 human… |
10 mg |
37291-10 |
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LNP023 (hydrochloride) |
A CFB inhibitor (IC50 = 10 nM); selective for CFB over a panel of 41 human… |
25 mg |
37291-25 |
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LNP023 (hydrochloride) |
A CFB inhibitor (IC50 = 10 nM); selective for CFB over a panel of 41 human… |
5 mg |
37291-5 |
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LNT 1 |
A FEN1 inhibitor (IC50 = 0.011 µM); selective for FEN1 over xeroderm… |
1 mg |
35803-1 |
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LNT 1 |
A FEN1 inhibitor (IC50 = 0.011 µM); selective for FEN1 over xeroderm… |
10 mg |
35803-10 |
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LNT 1 |
A FEN1 inhibitor (IC50 = 0.011 µM); selective for FEN1 over xeroderm… |
5 mg |
35803-5 |
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Lobaric Acid |
A depsidone metabolite; scavenges superoxide radicals in a cell-free assay… |
2.5 mg |
25205-25 |
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Lobaric Acid |
A depsidone metabolite; scavenges superoxide radicals in a cell-free assay… |
500 µg |
25205-500 |
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(-)-Lobelin (hydrochloride) |
An alkaloid with diverse biological activities; binds to nAChRs in rat bra… |
1 g |
29526-1 |
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(-)-Lobelin (hydrochloride) |
An alkaloid with diverse biological activities; binds to nAChRs in rat bra… |
250 mg |
29526-250 |
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(-)-Lobelin (hydrochloride) |
An alkaloid with diverse biological activities; binds to nAChRs in rat bra… |
500 mg |
29526-500 |
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LOC14 |
A PDI inhibitor (Kd = 62 nM); inhibits PDI chaperone activity in an insuli… |
10 mg |
17766-10 |
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LOC14 |
A PDI inhibitor (Kd = 62 nM); inhibits PDI chaperone activity in an insuli… |
100 mg |
17766-100 |
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LOC14 |
A PDI inhibitor (Kd = 62 nM); inhibits PDI chaperone activity in an insuli… |
25 mg |
17766-25 |
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LOC14 |
A PDI inhibitor (Kd = 62 nM); inhibits PDI chaperone activity in an insuli… |
50 mg |
17766-50 |
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