CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 3 of 1

Non-Antibody Products
Page 3 of 1,297
  • Records 101 - 150 of 64,815
Name Description Size Catalog #
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
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
Sales: sales@caymanchem.com

http://www.caymanchem.com

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