Non-Antibody Products — page 1 of 29,811



Non-Antibody Products
Page 1 of 29,811
  • Records 1 - 75 of 2,235,767
Name Description Size Catalog # Supplier
A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 50 mg 16081-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 1 mg 25605-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 10 mg 25605-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 5 mg 25605-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 1 mg 16499-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 5 mg 16499-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 500 µg 16499-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 1 mg 28279-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 10 mg 28279-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 25 mg 28279-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 5 mg 28279-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 1 mg 24119-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 10 mg 24119-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 25 mg 24119-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 5 mg 24119-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 1 mg 17358-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 10 mg 17358-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 5 mg 17358-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 1 mg 17382-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 10 mg 17382-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 25 mg 17382-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 5 mg 17382-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 1 mg 18715-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 10 mg 18715-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 5 mg 18715-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 500 µg 18715-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 1 mg 29972-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 10 mg 29972-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 5 mg 29972-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 500 µg 29972-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 1 mg 21256-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 10 mg 21256-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 25 mg 21256-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 5 mg 21256-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 10 mg 11900-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 25 mg 11900-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 5 mg 11900-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 50 mg 11900-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-770041 An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… 1 mg 32854-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-770041 An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… 5 mg 32854-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-77-01 A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… 1 mg 18396-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-77-01 A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… 10 mg 18396-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-77-01 A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… 25 mg 18396-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-77-01 A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… 5 mg 18396-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-771726 An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… 10 mg 14404-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-771726 An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… 25 mg 14404-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-771726 An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… 5 mg 14404-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-784168 A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… 1 mg 32855-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-784168 A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… 10 mg 32855-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-784168 A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… 25 mg 32855-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-784168 A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… 5 mg 32855-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-796260 A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… 1 mg 11606-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-796260 A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… 10 mg 11606-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-796260 A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… 5 mg 11606-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-803467 A sodium channel blocker with high-affinity and selectivity for inhibiting… 10 mg 10012588-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-803467 A sodium channel blocker with high-affinity and selectivity for inhibiting… 100 mg 10012588-100 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-803467 A sodium channel blocker with high-affinity and selectivity for inhibiting… 5 mg 10012588-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-803467 A sodium channel blocker with high-affinity and selectivity for inhibiting… 50 mg 10012588-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-804598 A potent and selective competitive antagonist of the P2X7 receptor (IC50s… 10 mg 20060-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-804598 A potent and selective competitive antagonist of the P2X7 receptor (IC50s… 25 mg 20060-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-804598 A potent and selective competitive antagonist of the P2X7 receptor (IC50s… 5 mg 20060-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-804598 A potent and selective competitive antagonist of the P2X7 receptor (IC50s… 50 mg 20060-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-834735 An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… 1 mg 11163-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-834735 An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… 10 mg 11163-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-834735 An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… 5 mg 11163-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-836339 A synthetic CB which has a higher affinity for the peripheral CB2 receptor… 1 mg 13898-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-836339 A synthetic CB which has a higher affinity for the peripheral CB2 receptor… 10 mg 13898-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-836339 A synthetic CB which has a higher affinity for the peripheral CB2 receptor… 5 mg 13898-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-839977 A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… 1 mg 30934-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-839977 A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… 10 mg 30934-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-839977 A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… 5 mg 30934-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-841720 A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… 1 mg 21807-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-841720 A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… 10 mg 21807-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-841720 A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… 5 mg 21807-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-867744 A positive allosteric modulator of α7 nAChRs; selective for α7… 10 mg 32974-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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