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

Non-Antibody Products
Page 1,275 of 1,297
  • Records 63,701 - 63,750 of 64,815
Name Description Size Catalog #
WWL70 A selective inhibitor of ABHD6 (IC50 = 70 nM); increases Ucp1 expression a… 5 mg 10011213-5 More Info
Wy 14643 An agonist of PPARα; selectively transactivates PPARα over PPA… 10 mg 70730-10 More Info
Wy 14643 An agonist of PPARα; selectively transactivates PPARα over PPA… 250 mg 70730-250 More Info
Wy 14643 An agonist of PPARα; selectively transactivates PPARα over PPA… 5 mg 70730-5 More Info
Wy 14643 An agonist of PPARα; selectively transactivates PPARα over PPA… 50 mg 70730-50 More Info
WYE-125132 An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… 1 mg 18372-1 More Info
WYE-125132 An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… 10 mg 18372-10 More Info
WYE-125132 An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… 5 mg 18372-5 More Info
WYE-125132 An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… 500 µg 18372-500 More Info
WYE-23 An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… 1 mg 21199-1 More Info
WYE-23 An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… 10 mg 21199-10 More Info
WYE-23 An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… 5 mg 21199-5 More Info
WYE-23 An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… 500 µg 21199-500 More Info
WYE-28 An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… 1 mg 21200-1 More Info
WYE-28 An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… 10 mg 21200-10 More Info
WYE-28 An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… 5 mg 21200-5 More Info
WYE-28 An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… 500 µg 21200-500 More Info
WYE-354 A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… 10 mg 13604-10 More Info
WYE-354 A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… 25 mg 13604-25 More Info
WYE-354 A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… 5 mg 13604-5 More Info
WYE-354 A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… 50 mg 13604-50 More Info
WYE-687 An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… 1 mg 29977-1 More Info
WYE-687 An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… 10 mg 29977-10 More Info
WYE-687 An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… 25 mg 29977-25 More Info
WYE-687 An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… 5 mg 29977-5 More Info
WZ3146 An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… 1 mg 23440-1 More Info
WZ3146 An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… 10 mg 23440-10 More Info
WZ3146 An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… 5 mg 23440-5 More Info
WZ3146 An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… 50 mg 23440-50 More Info
WZ4002 An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… 10 mg 16297-10 More Info
WZ4002 An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… 100 mg 16297-100 More Info
WZ4002 An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… 5 mg 16297-5 More Info
WZ4002 An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… 50 mg 16297-50 More Info
WZ4003 A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… 1 mg 19177-1 More Info
WZ4003 A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… 10 mg 19177-10 More Info
WZ4003 A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… 25 mg 19177-25 More Info
WZ4003 A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… 5 mg 19177-5 More Info
WZ8040 An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… 10 mg 30062-10 More Info
WZ8040 An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… 25 mg 30062-25 More Info
WZ8040 An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… 5 mg 30062-5 More Info
WZ8040 An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… 50 mg 30062-50 More Info
WZ811 A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… 1 mg 13639-1 More Info
WZ811 A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… 10 mg 13639-10 More Info
WZ811 A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… 25 mg 13639-25 More Info
WZ811 A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… 5 mg 13639-5 More Info
WZB117 An irreversible inhibitor of Glut1 that blocks glucose transport in divers… 10 mg 19900-10 More Info
WZB117 An irreversible inhibitor of Glut1 that blocks glucose transport in divers… 25 mg 19900-25 More Info
WZB117 An irreversible inhibitor of Glut1 that blocks glucose transport in divers… 5 mg 19900-5 More Info
WZB117 An irreversible inhibitor of Glut1 that blocks glucose transport in divers… 50 mg 19900-50 More Info
X-82 A multi-kinase inhibitor; inhibits VEGFR2, PDGFRβ, FLT3, and c-Kit (I… 1 mg 38765-1 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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