Kinsenoside |
A glycoside with diverse biological activities; increases adipose triglyce… |
5 mg |
25144-5 |
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KIRA6 |
An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… |
1 mg |
19151-1 |
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KIRA6 |
An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… |
10 mg |
19151-10 |
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KIRA6 |
An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… |
5 mg |
19151-5 |
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Kirenol |
A diterpenoid with diverse biological activities; inhibits Gram-positive a… |
10 mg |
26212-10 |
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Kirenol |
A diterpenoid with diverse biological activities; inhibits Gram-positive a… |
25 mg |
26212-25 |
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Kirenol |
A diterpenoid with diverse biological activities; inhibits Gram-positive a… |
5 mg |
26212-5 |
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Kirromycin |
An inhibitor of protein biosynthesis; inhibits isoleucine incorporation, p… |
1 mg |
25189-1 |
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Kisspeptin-54 (human) (trifluoroacetate salt) |
A peptide ligand of GPR54 (Kis = 1.81 and 1.45 nM for rat and human recept… |
500 µg |
24477-500 |
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Kisspeptin-10 (mouse, rat) |
A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… |
1 mg |
14036-1 |
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Kisspeptin-10 (mouse, rat) |
A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… |
10 mg |
14036-10 |
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Kisspeptin-10 (mouse, rat) |
A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… |
25 mg |
14036-25 |
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Kisspeptin-10 (mouse, rat) |
A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… |
5 mg |
14036-5 |
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Kisspeptin-234 (trifluoroacetate salt) |
A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… |
1 mg |
35633-1 |
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Kisspeptin-234 (trifluoroacetate salt) |
A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… |
10 mg |
35633-10 |
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Kisspeptin-234 (trifluoroacetate salt) |
A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… |
25 mg |
35633-25 |
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Kisspeptin-234 (trifluoroacetate salt) |
A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… |
5 mg |
35633-5 |
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Kisspeptin-10 (zebrafish) (trifluoroacetate salt) |
A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… |
1 mg |
35652-1 |
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Kisspeptin-10 (zebrafish) (trifluoroacetate salt) |
A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… |
10 mg |
35652-10 |
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Kisspeptin-10 (zebrafish) (trifluoroacetate salt) |
A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… |
25 mg |
35652-25 |
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Kisspeptin-10 (zebrafish) (trifluoroacetate salt) |
A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… |
5 mg |
35652-5 |
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KJ Pyr 9 |
A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… |
1 mg |
19116-1 |
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KJ Pyr 9 |
A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… |
10 mg |
19116-10 |
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KJ Pyr 9 |
A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… |
25 mg |
19116-25 |
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KJ Pyr 9 |
A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… |
5 mg |
19116-5 |
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KL001 |
A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… |
10 mg |
13878-10 |
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KL001 |
A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… |
25 mg |
13878-25 |
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KL001 |
A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… |
5 mg |
13878-5 |
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KLH45 |
An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… |
1 mg |
19889-1 |
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KLH45 |
An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… |
10 mg |
19889-10 |
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KLH45 |
An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… |
25 mg |
19889-25 |
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KLH45 |
An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… |
5 mg |
19889-5 |
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Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) |
A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… |
1 mg |
38166-1 |
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Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) |
A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… |
10 mg |
38166-10 |
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Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) |
A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… |
5 mg |
38166-5 |
More Info
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Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) |
A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… |
500 µg |
38166-500 |
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KM 11060 |
A F508del-CFTR corrector; increases cell surface expression and restores c… |
10 mg |
23481-10 |
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KM 11060 |
A F508del-CFTR corrector; increases cell surface expression and restores c… |
25 mg |
23481-25 |
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KM 11060 |
A F508del-CFTR corrector; increases cell surface expression and restores c… |
5 mg |
23481-5 |
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KM 11060 |
A F508del-CFTR corrector; increases cell surface expression and restores c… |
50 mg |
23481-50 |
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KM 233 |
Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… |
1 mg |
10640-1 |
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KM 233 |
Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… |
10 mg |
10640-10 |
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KM 233 |
Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… |
25 mg |
10640-25 |
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KM 233 |
Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… |
5 mg |
10640-5 |
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KML29 |
An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… |
10 mg |
11777-10 |
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KML29 |
An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… |
100 mg |
11777-100 |
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KML29 |
An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… |
5 mg |
11777-5 |
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KML29 |
An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… |
50 mg |
11777-50 |
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KMN-80 |
A selective, potent agonist of EP4 with an IC50 value of 3 nM (versus 1.4… |
1 mg |
15435-1 |
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KMN-80 |
A selective, potent agonist of EP4 with an IC50 value of 3 nM (versus 1.4… |
500 µg |
15435-500 |
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KN-62 |
A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) |
1 mg |
13318-1 |
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KN-62 |
A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) |
10 mg |
13318-10 |
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KN-62 |
A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) |
25 mg |
13318-25 |
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KN-62 |
A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) |
5 mg |
13318-5 |
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KN-93 |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
1 mg |
13319-1 |
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KN-93 |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
10 mg |
13319-10 |
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KN-93 |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
5 mg |
13319-5 |
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KN-92 (hydrochloride) |
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… |
1 mg |
9000890-1 |
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KN-92 (hydrochloride) |
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… |
10 mg |
9000890-10 |
More Info
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KN-92 (hydrochloride) |
An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… |
5 mg |
9000890-5 |
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KN-93 (hydrochloride) |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
1 mg |
13864-1 |
More Info
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KN-93 (hydrochloride) |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
10 mg |
13864-10 |
More Info
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KN-93 (hydrochloride) |
A selective inhibitor of CaMKII, competitively blocking CaM binding to the… |
5 mg |
13864-5 |
More Info
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KN-93 (phosphate) |
A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… |
1 mg |
21472-1 |
More Info
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KN-93 (phosphate) |
A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… |
10 mg |
21472-10 |
More Info
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KN-93 (phosphate) |
A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… |
25 mg |
21472-25 |
More Info
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KN-93 (phosphate) |
A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… |
5 mg |
21472-5 |
More Info
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Ko 143 |
A potent and selective inhibitor of BCRP, preventing the export of mitoxan… |
10 mg |
15215-10 |
More Info
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Ko 143 |
A potent and selective inhibitor of BCRP, preventing the export of mitoxan… |
25 mg |
15215-25 |
More Info
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Ko 143 |
A potent and selective inhibitor of BCRP, preventing the export of mitoxan… |
5 mg |
15215-5 |
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Ko 143 |
A potent and selective inhibitor of BCRP, preventing the export of mitoxan… |
50 mg |
15215-50 |
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KO947 |
An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… |
1 mg |
29213-1 |
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KO947 |
An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… |
10 mg |
29213-10 |
More Info
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KO947 |
An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… |
25 mg |
29213-25 |
More Info
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KO947 |
An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… |
5 mg |
29213-5 |
More Info
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