L-Leucine 4-methoxy-β-naphthylamide (hydrochloride) |
A cell-permeable substrate for aminopeptidase M and leucine aminopeptidase… |
250 mg |
16223-250 |
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L-Leucyl-L-Leucine methyl ester (hydrochloride) |
A lysosomal condensation product that selectively eliminates dipeptidyl pe… |
1 g |
16008-1 |
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L-Leucyl-L-Leucine methyl ester (hydrochloride) |
A lysosomal condensation product that selectively eliminates dipeptidyl pe… |
100 mg |
16008-100 |
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L-Leucyl-L-Leucine methyl ester (hydrochloride) |
A lysosomal condensation product that selectively eliminates dipeptidyl pe… |
250 mg |
16008-250 |
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LL-37 (human) (scrambled) (trifluoroacetate salt) |
A negative control for LL-37 (human),, |
1 mg |
37503-1 |
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LL-37 (human) (scrambled) (trifluoroacetate salt) |
A negative control for LL-37 (human),, |
10 mg |
37503-10 |
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LL-37 (human) (scrambled) (trifluoroacetate salt) |
A negative control for LL-37 (human),, |
5 mg |
37503-5 |
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LL-37 (18-37) (human) (trifluoroacetate salt) |
An antimicrobial peptide fragment of LL-37; active against S. aureus and C… |
1 mg |
36950-1 |
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LL-37 (18-37) (human) (trifluoroacetate salt) |
An antimicrobial peptide fragment of LL-37; active against S. aureus and C… |
10 mg |
36950-10 |
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LL-37 (18-37) (human) (trifluoroacetate salt) |
An antimicrobial peptide fragment of LL-37; active against S. aureus and C… |
25 mg |
36950-25 |
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LL-37 (18-37) (human) (trifluoroacetate salt) |
An antimicrobial peptide fragment of LL-37; active against S. aureus and C… |
5 mg |
36950-5 |
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LL-37 (human) (trifluoroacetate salt) |
An antimicrobial peptide; inhibits growth of Gram-positive E. coli D21 and… |
1 mg |
24461-1 |
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LL-37 (human) (trifluoroacetate salt) |
An antimicrobial peptide; inhibits growth of Gram-positive E. coli D21 and… |
500 µg |
24461-500 |
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LL-37 (13-37) (human) (trifluoroacetate salt) |
An anticancer peptide fragment of LL-37; inhibits the ATPase activity of A… |
1 mg |
36949-1 |
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LL-37 (13-37) (human) (trifluoroacetate salt) |
An anticancer peptide fragment of LL-37; inhibits the ATPase activity of A… |
10 mg |
36949-10 |
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LL-37 (13-37) (human) (trifluoroacetate salt) |
An anticancer peptide fragment of LL-37; inhibits the ATPase activity of A… |
25 mg |
36949-25 |
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LL-37 (13-37) (human) (trifluoroacetate salt) |
An anticancer peptide fragment of LL-37; inhibits the ATPase activity of A… |
5 mg |
36949-5 |
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LLP-3 |
A cell-permeable ligand of Survivin that blocks its interaction with Ran,… |
1 mg |
19088-1 |
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LLP-3 |
A cell-permeable ligand of Survivin that blocks its interaction with Ran,… |
5 mg |
19088-5 |
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LLY-283 |
A PRMT5 inhibitor (IC50 = 22 nM); selective for PRMT5 over a panel of 32 m… |
1 mg |
21596-1 |
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LLY-283 |
A PRMT5 inhibitor (IC50 = 22 nM); selective for PRMT5 over a panel of 32 m… |
10 mg |
21596-10 |
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LLY-283 |
A PRMT5 inhibitor (IC50 = 22 nM); selective for PRMT5 over a panel of 32 m… |
25 mg |
21596-25 |
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LLY-283 |
A PRMT5 inhibitor (IC50 = 22 nM); selective for PRMT5 over a panel of 32 m… |
5 mg |
21596-5 |
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LLY-507 |
A selective, cell-active, small molecule inhibitor of SMYD2 (IC50 = 15 nM)… |
1 mg |
16441-1 |
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LLY-507 |
A selective, cell-active, small molecule inhibitor of SMYD2 (IC50 = 15 nM)… |
10 mg |
16441-10 |
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LLY-507 |
A selective, cell-active, small molecule inhibitor of SMYD2 (IC50 = 15 nM)… |
25 mg |
16441-25 |
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LLY-507 |
A selective, cell-active, small molecule inhibitor of SMYD2 (IC50 = 15 nM)… |
5 mg |
16441-5 |
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L-Lysine-d3 (hydrochloride) |
An internal standard for the quantification of L-lysine by GC- or LC-MS |
1 mg |
34844-1 |
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L-Lysine-d3 (hydrochloride) |
An internal standard for the quantification of L-lysine by GC- or LC-MS |
10 mg |
34844-10 |
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L-Lysine-d3 (hydrochloride) |
An internal standard for the quantification of L-lysine by GC- or LC-MS |
25 mg |
34844-25 |
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L-Lysine-d3 (hydrochloride) |
An internal standard for the quantification of L-lysine by GC- or LC-MS |
5 mg |
34844-5 |
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L-Lysine (hydrochloride) |
An essential amino acid; reduces viral shedding in cats latently infected… |
100 g |
36455-100 |
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L-Lysine (hydrochloride) |
An essential amino acid; reduces viral shedding in cats latently infected… |
50 g |
36455-50 |
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L-Lysine (hydrochloride) |
An essential amino acid; reduces viral shedding in cats latently infected… |
500 g |
36455-500 |
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L-Lysine lactam (hydrochloride) |
A building block; has been used in the synthesis of HIV protease inhibitor… |
1 g |
31685-1 |
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L-Lysine lactam (hydrochloride) |
A building block; has been used in the synthesis of HIV protease inhibitor… |
100 mg |
31685-100 |
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L-Lysine lactam (hydrochloride) |
A building block; has been used in the synthesis of HIV protease inhibitor… |
50 mg |
31685-50 |
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L-Lysine lactam (hydrochloride) |
A building block; has been used in the synthesis of HIV protease inhibitor… |
500 mg |
31685-500 |
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LL-Z 1640-4 |
A resorcylic acid lactone with antiviral and antiprotozoan activity; used… |
1 mg |
19159-1 |
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LL-Z 1640-4 |
A resorcylic acid lactone with antiviral and antiprotozoan activity; used… |
5 mg |
19159-5 |
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LM-10 |
A TDO inhibitor (IC50 = 2 µM); selective for TDO over IDO, MAO-A, an… |
10 mg |
36291-10 |
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LM-10 |
A TDO inhibitor (IC50 = 2 µM); selective for TDO over IDO, MAO-A, an… |
25 mg |
36291-25 |
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LM-10 |
A TDO inhibitor (IC50 = 2 µM); selective for TDO over IDO, MAO-A, an… |
5 mg |
36291-5 |
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LM-10 |
A TDO inhibitor (IC50 = 2 µM); selective for TDO over IDO, MAO-A, an… |
50 mg |
36291-50 |
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LM22A-4 |
An agonist of TrkB (IC50 = 47 nM in a fluorescence anisotropy assay); sele… |
10 mg |
22082-10 |
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LM22A-4 |
An agonist of TrkB (IC50 = 47 nM in a fluorescence anisotropy assay); sele… |
25 mg |
22082-25 |
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LM22A-4 |
An agonist of TrkB (IC50 = 47 nM in a fluorescence anisotropy assay); sele… |
5 mg |
22082-5 |
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LM22A-4 |
An agonist of TrkB (IC50 = 47 nM in a fluorescence anisotropy assay); sele… |
50 mg |
22082-50 |
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LM11A-31 (hydrochloride) |
A p75NTR ligand; inhibits NGF binding to p75NTR-Fc (A2 = 1,192 nM); inhibi… |
10 mg |
21982-10 |
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LM11A-31 (hydrochloride) |
A p75NTR ligand; inhibits NGF binding to p75NTR-Fc (A2 = 1,192 nM); inhibi… |
25 mg |
21982-25 |
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