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

Non-Antibody Products
Page 1,277 of 1,297
  • Records 63,801 - 63,850 of 64,815
Name Description Size Catalog #
XAP044 An antagonist of mGluR7, inhibiting lateral amygdala long term potentiatio… 10 mg 19095-10 More Info
XAP044 An antagonist of mGluR7, inhibiting lateral amygdala long term potentiatio… 5 mg 19095-5 More Info
XAV939 A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… 1 mg 13596-1 More Info
XAV939 A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… 10 mg 13596-10 More Info
XAV939 A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… 25 mg 13596-25 More Info
XAV939 A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… 5 mg 13596-5 More Info
XCT790 A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… 1 mg 16035-1 More Info
XCT790 A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… 10 mg 16035-10 More Info
XCT790 A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… 5 mg 16035-5 More Info
XD14 A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… 10 mg 30740-10 More Info
XD14 A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… 25 mg 30740-25 More Info
XD14 A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… 5 mg 30740-5 More Info
XD14 A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… 50 mg 30740-50 More Info
XE 991 (hydrochloride) A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… 10 mg 14582-10 More Info
XE 991 (hydrochloride) A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… 5 mg 14582-5 More Info
XE 991 (hydrochloride) A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… 50 mg 14582-50 More Info
XEN445 A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… 1 mg 19144-1 More Info
XEN445 A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… 10 mg 19144-10 More Info
XEN445 A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… 5 mg 19144-5 More Info
Xenopsin A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… 1 mg 29968-1 More Info
Xenopsin A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… 10 mg 29968-10 More Info
Xenopsin A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… 5 mg 29968-5 More Info
Xestospongin C An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… 10 µg 64950-10 More Info
Xestospongin C An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… 100 µg 64950-100 More Info
Xestospongin C An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… 250 µg 64950-250 More Info
Xestospongin C An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… 50 µg 64950-50 More Info
X-Gal A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… 1 g 16495-1 More Info
X-Gal A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… 5 g 16495-5 More Info
X-Gal A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… 500 mg 16495-500 More Info
XIE62-1004 An inducer of autophagy; increases the number of p62 aggregates, as well a… 1 mg 40446-1 More Info
XIE62-1004 An inducer of autophagy; increases the number of p62 aggregates, as well a… 10 mg 40446-10 More Info
XIE62-1004 An inducer of autophagy; increases the number of p62 aggregates, as well a… 25 mg 40446-25 More Info
XIE62-1004 An inducer of autophagy; increases the number of p62 aggregates, as well a… 5 mg 40446-5 More Info
Ximelagatran An ester prodrug of melagatran, a potent, direct, and reversible thrombin… 1 mg 16862-1 More Info
Ximelagatran An ester prodrug of melagatran, a potent, direct, and reversible thrombin… 10 mg 16862-10 More Info
Ximelagatran An ester prodrug of melagatran, a potent, direct, and reversible thrombin… 5 mg 16862-5 More Info
XL019 A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… 1 mg 16298-1 More Info
XL019 A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… 10 mg 16298-10 More Info
XL019 A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… 25 mg 16298-25 More Info
XL019 A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… 5 mg 16298-5 More Info
XL092 A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… 10 mg 37749-10 More Info
XL092 A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… 25 mg 37749-25 More Info
XL092 A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… 5 mg 37749-5 More Info
XL147 A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… 10 mg 18011-10 More Info
XL147 A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… 25 mg 18011-25 More Info
XL147 A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… 5 mg 18011-5 More Info
XL184 A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… 1 mg 18464-1 More Info
XL184 A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… 10 mg 18464-10 More Info
XL184 A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… 5 mg 18464-5 More Info
XL184 A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… 50 mg 18464-50 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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