CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 2 of 865
Non-Antibody Products
Page 2 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 1 mg | 17358-1 | More Info |
| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 10 mg | 17358-10 | More Info |
| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 5 mg | 17358-5 | More Info |
| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 1 mg | 17382-1 | More Info |
| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 10 mg | 17382-10 | More Info |
| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 25 mg | 17382-25 | More Info |
| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 5 mg | 17382-5 | More Info |
| A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 1 mg | 18715-1 | More Info |
| A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 10 mg | 18715-10 | More Info |
| A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 5 mg | 18715-5 | More Info |
| A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 500 µg | 18715-500 | More Info |
| A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 1 mg | 29972-1 | More Info |
| A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 10 mg | 29972-10 | More Info |
| A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 5 mg | 29972-5 | More Info |
| A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 500 µg | 29972-500 | More Info |
| A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 1 mg | 21256-1 | More Info |
| A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 10 mg | 21256-10 | More Info |
| A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 25 mg | 21256-25 | More Info |
| A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 5 mg | 21256-5 | More Info |
| A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 10 mg | 11900-10 | More Info |
| A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 25 mg | 11900-25 | More Info |
| A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 5 mg | 11900-5 | More Info |
| A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 50 mg | 11900-50 | More Info |
| A-770041 | An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… | 1 mg | 32854-1 | More Info |
| A-770041 | An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… | 5 mg | 32854-5 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 1 mg | 18396-1 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 10 mg | 18396-10 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 25 mg | 18396-25 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 5 mg | 18396-5 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 10 mg | 14404-10 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 25 mg | 14404-25 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 5 mg | 14404-5 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 1 mg | 32855-1 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 10 mg | 32855-10 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 25 mg | 32855-25 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 5 mg | 32855-5 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 1 mg | 11606-1 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 10 mg | 11606-10 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 5 mg | 11606-5 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 10 mg | 10012588-10 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 100 mg | 10012588-100 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 5 mg | 10012588-5 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 50 mg | 10012588-50 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 10 mg | 20060-10 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 25 mg | 20060-25 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 5 mg | 20060-5 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 50 mg | 20060-50 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 1 mg | 11163-1 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 10 mg | 11163-10 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 5 mg | 11163-5 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 1 mg | 13898-1 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 10 mg | 13898-10 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 5 mg | 13898-5 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 1 mg | 30934-1 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 10 mg | 30934-10 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 5 mg | 30934-5 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 1 mg | 21807-1 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 10 mg | 21807-10 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 5 mg | 21807-5 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 10 mg | 32974-10 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 100 mg | 32974-100 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 50 mg | 32974-50 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 1 mg | 10012708-1 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 10 mg | 10012708-10 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 25 mg | 10012708-25 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 5 mg | 10012708-5 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 10 mg | 19123-10 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 5 mg | 19123-5 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 50 mg | 19123-50 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 1 mg | 26378-1 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 10 mg | 26378-10 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 25 mg | 26378-25 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 5 mg | 26378-5 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 10 mg | 15207-10 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 25 mg | 15207-25 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
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http://www.caymanchem.com
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