kb-NB77-78 |
An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… |
10 mg |
21562-10 |
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kb-NB77-78 |
An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… |
25 mg |
21562-25 |
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kb-NB77-78 |
An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… |
5 mg |
21562-5 |
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KB-R7943 (mesylate) |
A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… |
10 mg |
16352-10 |
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KB-R7943 (mesylate) |
A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… |
5 mg |
16352-5 |
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KB-R7943 (mesylate) |
A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… |
50 mg |
16352-50 |
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K252c |
A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… |
1 mg |
13514-1 |
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K252c |
A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… |
10 mg |
13514-10 |
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K252c |
A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… |
5 mg |
13514-5 |
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KC01 |
A covalent inhibitor of ABHD16A (IC50s = 90 and 520 nM for human and mouse… |
1 mg |
17364-1 |
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KC01 |
A covalent inhibitor of ABHD16A (IC50s = 90 and 520 nM for human and mouse… |
500 µg |
17364-500 |
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KC02 |
An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… |
1 mg |
17365-1 |
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KC02 |
An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… |
100 µg |
17365-100 |
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KC02 |
An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… |
500 µg |
17365-500 |
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KC7F2 |
An inhibitor of HIF-1α protein translation; suppresses phosphorylati… |
10 mg |
14123-10 |
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KC7F2 |
An inhibitor of HIF-1α protein translation; suppresses phosphorylati… |
5 mg |
14123-5 |
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KC7F2 |
An inhibitor of HIF-1α protein translation; suppresses phosphorylati… |
50 mg |
14123-50 |
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K252d |
An indolocarbazole alkaloid found in Nocardiopsis; a PKC inhibitor; inhibi… |
1 mg |
28469-1 |
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KD 025 |
A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… |
10 mg |
17055-10 |
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KD 025 |
A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… |
100 mg |
17055-100 |
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KD 025 |
A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… |
25 mg |
17055-25 |
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KD 025 |
A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… |
50 mg |
17055-50 |
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KD 5170 |
A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… |
1 mg |
13214-1 |
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KD 5170 |
A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… |
10 mg |
13214-10 |
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KD 5170 |
A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… |
25 mg |
13214-25 |
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KD 5170 |
A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… |
5 mg |
13214-5 |
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KDdiA-PC |
Oxidized LDL (oxLDL) particles contain low molecular weight species which… |
1 mg |
62935-1 |
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KDdiA-PC |
Oxidized LDL (oxLDL) particles contain low molecular weight species which… |
10 mg |
62935-10 |
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KDdiA-PC |
Oxidized LDL (oxLDL) particles contain low molecular weight species which… |
5 mg |
62935-5 |
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KDdiA-PC |
Oxidized LDL (oxLDL) particles contain low molecular weight species which… |
500 µg |
62935-500 |
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KDM5-C70 |
An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… |
10 mg |
36817-10 |
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KDM5-C70 |
An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… |
25 mg |
36817-25 |
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KDM5-C70 |
An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… |
5 mg |
36817-5 |
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KDM5-C70 |
An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… |
50 mg |
36817-50 |
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KDM4D-IN-1 |
An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… |
1 mg |
37431-1 |
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KDM4D-IN-1 |
An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… |
10 mg |
37431-10 |
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KDM4D-IN-1 |
An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… |
25 mg |
37431-25 |
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KDM4D-IN-1 |
An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… |
5 mg |
37431-5 |
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Kdo2-Lipid A (sodium salt) |
The active component of LPS; selectively induces Il-6 expression in wild-t… |
1 mg |
10860-1 |
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KDU691 |
An antimalarial compound; inhibits the activity of recombinant P. vivax PI… |
1 mg |
29019-1 |
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KDU691 |
An antimalarial compound; inhibits the activity of recombinant P. vivax PI… |
10 mg |
29019-10 |
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KDU691 |
An antimalarial compound; inhibits the activity of recombinant P. vivax PI… |
25 mg |
29019-25 |
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KDU691 |
An antimalarial compound; inhibits the activity of recombinant P. vivax PI… |
5 mg |
29019-5 |
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Keap1 (human, recombinant) |
Source: Recombinant human N-terminal His-GST-tagged Keap1 expressed in ins… |
100 µg |
32035-100 |
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KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) |
A peptide fragment of β-casein; can be produced by the protease M fro… |
10 mg |
38850-10 |
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KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) |
A peptide fragment of β-casein; can be produced by the protease M fro… |
100 mg |
38850-100 |
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KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) |
A peptide fragment of β-casein; can be produced by the protease M fro… |
250 mg |
38850-250 |
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KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) |
A peptide fragment of β-casein; can be produced by the protease M fro… |
50 mg |
38850-50 |
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Kemptide |
A synthetic heptapeptide that acts as a specific substrate for PKA |
1 mg |
15555-1 |
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Kemptide |
A synthetic heptapeptide that acts as a specific substrate for PKA |
10 mg |
15555-10 |
More Info
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