CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 974 of 1
Non-Antibody Products
Page 974 of 1,304
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Pitstop2 | An inhibitor of the amphiphysin-clathrin interaction (IC50 = 12 µM);… | 5 mg | 23885-5 | More Info |
| Pivaloyl fentanyl (hydrochloride) | An analytical reference standard categorized as an opioid; regulated as a… | 1 mg | 22991-1 | More Info |
| Pivaloyl fentanyl (hydrochloride) | An analytical reference standard categorized as an opioid; regulated as a… | 5 mg | 22991-5 | More Info |
| Pixantrone-d8 (maleate) | An internal standard for the quantification of pixantrone by GC- or LC-MS | 1 mg | 33292-1 | More Info |
| Pixantrone-d8 (maleate) | An internal standard for the quantification of pixantrone by GC- or LC-MS | 5 mg | 33292-5 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 1 mg | 20055-1 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 10 mg | 20055-10 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 25 mg | 20055-25 | More Info |
| Pixantrone (maleate) | A DNA topoisomerase II inhibitor; induces SV40 DNA cleavage in the presenc… | 5 mg | 20055-5 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 1 g | 20765-1 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 100 mg | 20765-100 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 250 mg | 20765-250 | More Info |
| Pizotifen (malate) | A triptan with high affinity for serotonin and dopamine receptors (Kis = 7… | 500 mg | 20765-500 | More Info |
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 1 mg | 14440-1 | More Info |
| PJ-34 (hydrochloride) | An inhibitor of PARPs which can be used in cells or in animals; binds and… | 10 mg | 14440-10 | More Info |
| 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 |
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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