CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 646 of 865
Non-Antibody Products
Page 646 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 25 mg | 14440-25 | More Info |
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 5 mg | 14440-5 | More Info |
| PK11000 | A stabilizer of mutant p53; covalently binds to Cys182 and Cys277, increas… | 100 mg | 37306-100 | More Info |
| PK11000 | A stabilizer of mutant p53; covalently binds to Cys182 and Cys277, increas… | 250 mg | 37306-250 | More Info |
| PK11000 | A stabilizer of mutant p53; covalently binds to Cys182 and Cys277, increas… | 500 mg | 37306-500 | More Info |
| PK11195 | Binds the peripheral benzodiazepine receptor, TSPO, with selectivity and h… | 10 mg | 10525-10 | More Info |
| PK11195 | Binds the peripheral benzodiazepine receptor, TSPO, with selectivity and h… | 50 mg | 10525-50 | More Info |
| PK68 | A RIPK1 inhibitor (IC50 = 90 nM); selective for RIPK1 over RIPK3 and a pan… | 10 mg | 36653-10 | More Info |
| PK68 | A RIPK1 inhibitor (IC50 = 90 nM); selective for RIPK1 over RIPK3 and a pan… | 25 mg | 36653-25 | More Info |
| PK68 | A RIPK1 inhibitor (IC50 = 90 nM); selective for RIPK1 over RIPK3 and a pan… | 5 mg | 36653-5 | More Info |
| PK68 | A RIPK1 inhibitor (IC50 = 90 nM); selective for RIPK1 over RIPK3 and a pan… | 50 mg | 36653-50 | More Info |
| PKA Inhibitor Fragment (6-22) amide | A synthetic peptide inhibitor of PKA (Ki = 1.7 nM) | 1 mg | 17486-1 | More Info |
| PKA Inhibitor Fragment (6-22) amide | A synthetic peptide inhibitor of PKA (Ki = 1.7 nM) | 10 mg | 17486-10 | More Info |
| PKA Inhibitor Fragment (6-22) amide | A synthetic peptide inhibitor of PKA (Ki = 1.7 nM) | 5 mg | 17486-5 | More Info |
| PKA Inhibitor Fragment (6-22) amide | A synthetic peptide inhibitor of PKA (Ki = 1.7 nM) | 500 µg | 17486-500 | More Info |
| PKA Inhibitor (5-24) (trifluoroacetate salt) | A synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase) (Ki =… | 1 mg | 15996-1 | More Info |
| PKA Inhibitor (5-24) (trifluoroacetate salt) | A synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase) (Ki =… | 5 mg | 15996-5 | More Info |
| PKA Inhibitor (5-24) (trifluoroacetate salt) | A synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase) (Ki =… | 500 µg | 15996-500 | More Info |
| PKC 412 | A cell-permeable, reversible inhibitor of several kinases, including PKC&a… | 1 mg | 10459-1 | More Info |
| PKC 412 | A cell-permeable, reversible inhibitor of several kinases, including PKC&a… | 10 mg | 10459-10 | More Info |
| PKC 412 | A cell-permeable, reversible inhibitor of several kinases, including PKC&a… | 25 mg | 10459-25 | More Info |
| PKC 412 | A cell-permeable, reversible inhibitor of several kinases, including PKC&a… | 5 mg | 10459-5 | More Info |
| PKC-9 | A PCKζ inhibitor; 8,000-, 20,671-, 711-, 918-, 1,895-, 12,424-, 10-,… | 1 mg | 25556-1 | More Info |
| PKC-9 | A PCKζ inhibitor; 8,000-, 20,671-, 711-, 918-, 1,895-, 12,424-, 10-,… | 10 mg | 25556-10 | More Info |
| PKC-9 | A PCKζ inhibitor; 8,000-, 20,671-, 711-, 918-, 1,895-, 12,424-, 10-,… | 5 mg | 25556-5 | More Info |
| PKCα (C2-4) Inhibitor Peptide | A synthetic peptide that blocks PKC activity in HepG2 cells stimulated wit… | 1 mg | 17478-1 | More Info |
| PKCα (C2-4) Inhibitor Peptide | A synthetic peptide that blocks PKC activity in HepG2 cells stimulated wit… | 5 mg | 17478-5 | More Info |
| PKCα (C2-4) Inhibitor Peptide | A synthetic peptide that blocks PKC activity in HepG2 cells stimulated wit… | 500 µg | 17478-500 | More Info |
| PKCα (human, recombinant) | Source: Active recombinant human N-terminal GST-tagged PKCα expresse… | 10 µg | 32563-10 | More Info |
| PKCβ Inhibitor | A PKCβ Inhibitor (IC50s = 21 and 5 nM, respectively); selective for P… | 10 mg | 35494-10 | More Info |
| PKCβ Inhibitor | A PKCβ Inhibitor (IC50s = 21 and 5 nM, respectively); selective for P… | 25 mg | 35494-25 | More Info |
| PKCβ Inhibitor | A PKCβ Inhibitor (IC50s = 21 and 5 nM, respectively); selective for P… | 5 mg | 35494-5 | More Info |
| PKCβ Inhibitor | A PKCβ Inhibitor (IC50s = 21 and 5 nM, respectively); selective for P… | 50 mg | 35494-50 | More Info |
| PKCδ Substrate (trifluoroacetate salt) | A peptide substrate for PKCδ; has been used to monitor PKCδ ac… | 1 mg | 37513-1 | More Info |
| PKCδ Substrate (trifluoroacetate salt) | A peptide substrate for PKCδ; has been used to monitor PKCδ ac… | 10 mg | 37513-10 | More Info |
| PKCδ Substrate (trifluoroacetate salt) | A peptide substrate for PKCδ; has been used to monitor PKCδ ac… | 5 mg | 37513-5 | More Info |
| PKCε Inhibitor Peptide | A synthetic peptide corresponding to an amino acid sequence found in the a… | 1 mg | 17476-1 | More Info |
| PKCε Inhibitor Peptide | A synthetic peptide corresponding to an amino acid sequence found in the a… | 10 mg | 17476-10 | More Info |
| PKCε Inhibitor Peptide | A synthetic peptide corresponding to an amino acid sequence found in the a… | 5 mg | 17476-5 | More Info |
| PKCε Inhibitor Peptide | A synthetic peptide corresponding to an amino acid sequence found in the a… | 500 µg | 17476-500 | More Info |
| PKCε Inhibitor Scramble Peptide | A negative control for PKCε inhibitor peptide; a scrambled peptide… | 1 mg | 31761-1 | More Info |
| PKCθ Inhibitor (hydrochloride) | A PKCθ inhibitor (IC50 = 18 nM) | 1 mg | 36165-1 | More Info |
| PKCθ Inhibitor (hydrochloride) | A PKCθ inhibitor (IC50 = 18 nM) | 10 mg | 36165-10 | More Info |
| PKCθ Inhibitor (hydrochloride) | A PKCθ inhibitor (IC50 = 18 nM) | 25 mg | 36165-25 | More Info |
| PKCθ Inhibitor (hydrochloride) | A PKCθ inhibitor (IC50 = 18 nM) | 5 mg | 36165-5 | More Info |
| PKCθ Pseudosubstrate Inhibitor | A synthetic peptide that corresponds to amino acid residues of the pseudos… | 1 mg | 17483-1 | More Info |
| PKCθ Pseudosubstrate Inhibitor | A synthetic peptide that corresponds to amino acid residues of the pseudos… | 500 µg | 17483-500 | More Info |
| PKCζ Pseudosubstrate Inhibitor | A synthetic peptide that that selectively, reversibly, and substrate-compe… | 1 mg | 17482-1 | More Info |
| PKCζ Pseudosubstrate Inhibitor | A synthetic peptide that that selectively, reversibly, and substrate-compe… | 5 mg | 17482-5 | More Info |
| PKCζ Pseudosubstrate Inhibitor | A synthetic peptide that that selectively, reversibly, and substrate-compe… | 500 µg | 17482-500 | More Info |
| PKF118-310 | An inhibitor of the Tcf4-β-catenin protein interaction; disrupts bind… | 1 mg | 22440-1 | More Info |
| PKF118-310 | An inhibitor of the Tcf4-β-catenin protein interaction; disrupts bind… | 10 mg | 22440-10 | More Info |
| PKF118-310 | An inhibitor of the Tcf4-β-catenin protein interaction; disrupts bind… | 5 mg | 22440-5 | More Info |
| PKG Drug G1 | A PKGIα activator; induces relaxation in U-46619-precontracted mesen… | 10 mg | 29768-10 | More Info |
| PKG Drug G1 | A PKGIα activator; induces relaxation in U-46619-precontracted mesen… | 100 mg | 29768-100 | More Info |
| PKG Drug G1 | A PKGIα activator; induces relaxation in U-46619-precontracted mesen… | 5 mg | 29768-5 | More Info |
| PKG Drug G1 | A PKGIα activator; induces relaxation in U-46619-precontracted mesen… | 50 mg | 29768-50 | More Info |
| PKG Inhibitor | A specific cGMP-dependent PKG inhibitor (Ki = 86 µM); a nonphosphory… | 1 mg | 15995-1 | More Info |
| PKG Inhibitor | A specific cGMP-dependent PKG inhibitor (Ki = 86 µM); a nonphosphory… | 10 mg | 15995-10 | More Info |
| PKG Inhibitor | A specific cGMP-dependent PKG inhibitor (Ki = 86 µM); a nonphosphory… | 5 mg | 15995-5 | More Info |
| PKI-166 | An inhibitor of EGFR (IC50 = 0.0007 µM for the intracellular kinase… | 1 mg | 21896-1 | More Info |
| PKI-166 | An inhibitor of EGFR (IC50 = 0.0007 µM for the intracellular kinase… | 10 mg | 21896-10 | More Info |
| PKI-166 | An inhibitor of EGFR (IC50 = 0.0007 µM for the intracellular kinase… | 25 mg | 21896-25 | More Info |
| PKI-166 | An inhibitor of EGFR (IC50 = 0.0007 µM for the intracellular kinase… | 5 mg | 21896-5 | More Info |
| PKI-402 | A dual inhibitor of PI3K and mTOR (IC50s = 1.4, 9.2, and 1.7 nM for PI3K&a… | 1 mg | 27664-1 | More Info |
| PKI-402 | A dual inhibitor of PI3K and mTOR (IC50s = 1.4, 9.2, and 1.7 nM for PI3K&a… | 10 mg | 27664-10 | More Info |
| PKI-402 | A dual inhibitor of PI3K and mTOR (IC50s = 1.4, 9.2, and 1.7 nM for PI3K&a… | 25 mg | 27664-25 | More Info |
| PKI-402 | A dual inhibitor of PI3K and mTOR (IC50s = 1.4, 9.2, and 1.7 nM for PI3K&a… | 5 mg | 27664-5 | More Info |
| PKI (14-22) amide (myristoylated) (trifluoroacetate salt) | A PKA inhibitor; inhibits PKA activity in mouse brain or spinal cord lysat… | 1 mg | 34431-1 | More Info |
| PKI (14-22) amide (myristoylated) (trifluoroacetate salt) | A PKA inhibitor; inhibits PKA activity in mouse brain or spinal cord lysat… | 5 mg | 34431-5 | More Info |
| PKI (14-22) amide (myristoylated) (trifluoroacetate salt) | A PKA inhibitor; inhibits PKA activity in mouse brain or spinal cord lysat… | 500 µg | 34431-500 | More Info |
| PKI-179 (hydrochloride) | A dual PI3K and mTOR inhibitor; inhibits PI3K (IC50s = 8, 24, 17, and 74 n… | 1 mg | 21202-1 | More Info |
| PKI-179 (hydrochloride) | A dual PI3K and mTOR inhibitor; inhibits PI3K (IC50s = 8, 24, 17, and 74 n… | 10 mg | 21202-10 | More Info |
| PKI-179 (hydrochloride) | A dual PI3K and mTOR inhibitor; inhibits PI3K (IC50s = 8, 24, 17, and 74 n… | 5 mg | 21202-5 | More Info |
| PK7242 (maleate) | An inducer of reactivation of mutant p53 in cancer cells that induces grow… | 1 mg | 17230-1 | 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
Sales: sales@caymanchem.com
http://www.caymanchem.com
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