CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 493 of 1
Non-Antibody Products
Page 493 of 1,297
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Fructose-1,6-bisphosphatase-1 Inhibitor | A cell-permeable benzoxazolo-sulfonamide compound that blocks human FBPase… | 10 mg | 18860-10 | More Info |
| Fructose-1,6-bisphosphatase-1 Inhibitor | A cell-permeable benzoxazolo-sulfonamide compound that blocks human FBPase… | 5 mg | 18860-5 | More Info |
| Fructose-1,6-bisphosphatase-1 Inhibitor | A cell-permeable benzoxazolo-sulfonamide compound that blocks human FBPase… | 50 mg | 18860-50 | More Info |
| Fruquintinib | A VEGFR inhibitor (IC50s = 33, 35, and 0.5 nM for VEGFR1, -2, and -3, resp… | 10 mg | 29425-10 | More Info |
| Fruquintinib | A VEGFR inhibitor (IC50s = 33, 35, and 0.5 nM for VEGFR1, -2, and -3, resp… | 100 mg | 29425-100 | More Info |
| Fruquintinib | A VEGFR inhibitor (IC50s = 33, 35, and 0.5 nM for VEGFR1, -2, and -3, resp… | 250 mg | 29425-250 | More Info |
| Fruquintinib | A VEGFR inhibitor (IC50s = 33, 35, and 0.5 nM for VEGFR1, -2, and -3, resp… | 50 mg | 29425-50 | More Info |
| FSB | A fluorescent probe; has been used for the detection of amyloid plaques in… | 5 mg | 10651-5 | More Info |
| FSEN1 | An inhibitor of FSP1 (IC50 = 313 nM); selective for FSP1 over NQO1 (IC50 =… | 1 mg | 38025-1 | More Info |
| FSEN1 | An inhibitor of FSP1 (IC50 = 313 nM); selective for FSP1 over NQO1 (IC50 =… | 10 mg | 38025-10 | More Info |
| FSEN1 | An inhibitor of FSP1 (IC50 = 313 nM); selective for FSP1 over NQO1 (IC50 =… | 25 mg | 38025-25 | More Info |
| FSEN1 | An inhibitor of FSP1 (IC50 = 313 nM); selective for FSP1 over NQO1 (IC50 =… | 5 mg | 38025-5 | More Info |
| FSLLRY-amide | A peptide antagonist of PAR2 which blocks activation by trypsin (IC50 = ~5… | 1 mg | 14709-1 | More Info |
| FSLLRY-amide | A peptide antagonist of PAR2 which blocks activation by trypsin (IC50 = ~5… | 10 mg | 14709-10 | More Info |
| FSLLRY-amide | A peptide antagonist of PAR2 which blocks activation by trypsin (IC50 = ~5… | 25 mg | 14709-25 | More Info |
| FSLLRY-amide | A peptide antagonist of PAR2 which blocks activation by trypsin (IC50 = ~5… | 5 mg | 14709-5 | More Info |
| FSL-1 (trifluoroacetate salt) | A synthetic lipopeptide agonist of TLR2 / TLR6; increases NF-κB acti… | 1 mg | 24220-1 | More Info |
| FSL-1 (trifluoroacetate salt) | A synthetic lipopeptide agonist of TLR2 / TLR6; increases NF-κB acti… | 5 mg | 24220-5 | More Info |
| FSL-1 (trifluoroacetate salt) | A synthetic lipopeptide agonist of TLR2 / TLR6; increases NF-κB acti… | 500 µg | 24220-500 | More Info |
| FSP1 Fluorescent Inhibitor Screening Assay Kit | Cayman's FSP1 Fluorescent Inhibitor Screening Assay Kit provides a robust… | 384 Well | 701900-384WELLS | More Info |
| FSP1 Fluorescent Inhibitor Screening Assay Kit | Cayman's FSP1 Fluorescent Inhibitor Screening Assay Kit provides a robust… | 96 Well | 701900-96WELLS | More Info |
| FSP1 (human, recombinant) | Source: Active recombinant N-terminal His-tagged human FSP1 expressed in E… | 50 µg | 29611-50 | More Info |
| FT113 | A FASN inhibitor (IC50 = 213 nM); inhibits the proliferation of PC3 and MV… | 10 mg | 37545-10 | More Info |
| FT113 | A FASN inhibitor (IC50 = 213 nM); inhibits the proliferation of PC3 and MV… | 25 mg | 37545-25 | More Info |
| FT113 | A FASN inhibitor (IC50 = 213 nM); inhibits the proliferation of PC3 and MV… | 5 mg | 37545-5 | More Info |
| FT113 | A FASN inhibitor (IC50 = 213 nM); inhibits the proliferation of PC3 and MV… | 50 mg | 37545-50 | More Info |
| FT709 | A USP9X inhibitor (IC50 = 82 nM); selective for USP9X over a panel of 20 d… | 1 mg | 39971-1 | More Info |
| FT709 | A USP9X inhibitor (IC50 = 82 nM); selective for USP9X over a panel of 20 d… | 10 mg | 39971-10 | More Info |
| FT709 | A USP9X inhibitor (IC50 = 82 nM); selective for USP9X over a panel of 20 d… | 5 mg | 39971-5 | More Info |
| FTAC6 | A detergent used to stabilize membrane proteins; CMC = 0.37 mM; has been u… | 250 mg | 24786-250 | More Info |
| FTAC6 | A detergent used to stabilize membrane proteins; CMC = 0.37 mM; has been u… | 500 mg | 24786-500 | More Info |
| FTAC8 | A detergent used to stabilize membrane proteins; CMC = 0.02 mM; has been u… | 250 mg | 24787-250 | More Info |
| FTase Inhibitor I | A potent and selective FTase inhibitor (IC50 = 21 nM); greater than 30-fol… | 1 mg | 22755-1 | More Info |
| FTase Inhibitor I | A potent and selective FTase inhibitor (IC50 = 21 nM); greater than 30-fol… | 500 µg | 22755-500 | More Info |
| FTase Inhibitor II (trifluoroacetate salt) | A cell-permeable analog of FPP that potently inhibits FTase (IC50 = 50-75… | 1 mg | 16607-1 | More Info |
| FTase Inhibitor II (trifluoroacetate salt) | A cell-permeable analog of FPP that potently inhibits FTase (IC50 = 50-75… | 5 mg | 16607-5 | More Info |
| FTI-276 (trifluoroacetate salt) | A peptidomimetic inhibitor of FTase (IC50 = 500 pM); selective for FTase o… | 1 mg | 10011661-1 | More Info |
| FTI-276 (trifluoroacetate salt) | A peptidomimetic inhibitor of FTase (IC50 = 500 pM); selective for FTase o… | 10 mg | 10011661-10 | More Info |
| FTI-276 (trifluoroacetate salt) | A peptidomimetic inhibitor of FTase (IC50 = 500 pM); selective for FTase o… | 5 mg | 10011661-5 | More Info |
| FTO (human, recombinant) | Source: Recombinant N-terminal histidine-tagged FTO purified from E. coli… | 100 µg | 26340-100 | More Info |
| F1 (trifluoroacetate salt) | An anti-inflammatory peptide; inhibits LPS-induced phosphorylation of IKK&… | 1 mg | 35846-1 | More Info |
| F1 (trifluoroacetate salt) | An anti-inflammatory peptide; inhibits LPS-induced phosphorylation of IKK&… | 10 mg | 35846-10 | More Info |
| F1 (trifluoroacetate salt) | An anti-inflammatory peptide; inhibits LPS-induced phosphorylation of IKK&… | 25 mg | 35846-25 | More Info |
| F1 (trifluoroacetate salt) | An anti-inflammatory peptide; inhibits LPS-induced phosphorylation of IKK&… | 5 mg | 35846-5 | More Info |
| F9170 (trifluoroacetate salt) | An antiviral peptide; binds to the LLP1 domain within the HIV-1 envelope p… | 1 mg | 36962-1 | More Info |
| F9170 (trifluoroacetate salt) | An antiviral peptide; binds to the LLP1 domain within the HIV-1 envelope p… | 10 mg | 36962-10 | More Info |
| F9170 (trifluoroacetate salt) | An antiviral peptide; binds to the LLP1 domain within the HIV-1 envelope p… | 25 mg | 36962-25 | More Info |
| F9170 (trifluoroacetate salt) | An antiviral peptide; binds to the LLP1 domain within the HIV-1 envelope p… | 5 mg | 36962-5 | More Info |
| FTT5 | A lipid-like compound; LLNs containing FTT5 and encapsulating an mRNA repo… | 1 mg | 37413-1 | More Info |
| FTT5 | A lipid-like compound; LLNs containing FTT5 and encapsulating an mRNA repo… | 5 mg | 37413-5 | 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
Return to Profile