CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 797 of 865
Non-Antibody Products
Page 797 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| TG003 | A novel benzothiazole compound that inhibits Clk1 / Sty and Clk4 (IC50 = 2… | 25 mg | 10398-25 | More Info |
| TG003 | A novel benzothiazole compound that inhibits Clk1 / Sty and Clk4 (IC50 = 2… | 5 mg | 10398-5 | More Info |
| TG100713 | An inhibitor of PI3K; (IC50s = 50, 24, 165, and 215 nM for PI3Kγ, PI… | 1 mg | 30195-1 | More Info |
| TG100713 | An inhibitor of PI3K; (IC50s = 50, 24, 165, and 215 nM for PI3Kγ, PI… | 10 mg | 30195-10 | More Info |
| TG100713 | An inhibitor of PI3K; (IC50s = 50, 24, 165, and 215 nM for PI3Kγ, PI… | 25 mg | 30195-25 | More Info |
| TG100713 | An inhibitor of PI3K; (IC50s = 50, 24, 165, and 215 nM for PI3Kγ, PI… | 5 mg | 30195-5 | More Info |
| TG101209 | A potent inhibitor of the tyrosine kinases JAK2, FLT3, RET, and JAK3 (IC50… | 1 mg | 14696-1 | More Info |
| TG101209 | A potent inhibitor of the tyrosine kinases JAK2, FLT3, RET, and JAK3 (IC50… | 10 mg | 14696-10 | More Info |
| TG101209 | A potent inhibitor of the tyrosine kinases JAK2, FLT3, RET, and JAK3 (IC50… | 25 mg | 14696-25 | More Info |
| TG101209 | A potent inhibitor of the tyrosine kinases JAK2, FLT3, RET, and JAK3 (IC50… | 5 mg | 14696-5 | More Info |
| TG101348 | A JAK2 inhibitor (IC50 = 3 nM for wild-type and JAK2V617F enzymes); is 35-… | 1 mg | 16289-1 | More Info |
| TG101348 | A JAK2 inhibitor (IC50 = 3 nM for wild-type and JAK2V617F enzymes); is 35-… | 10 mg | 16289-10 | More Info |
| TG101348 | A JAK2 inhibitor (IC50 = 3 nM for wild-type and JAK2V617F enzymes); is 35-… | 25 mg | 16289-25 | More Info |
| TG101348 | A JAK2 inhibitor (IC50 = 3 nM for wild-type and JAK2V617F enzymes); is 35-… | 5 mg | 16289-5 | More Info |
| TG2-179-1 | A BAP1 inhibitor; inhibits BAP1 deubiquitinase activity in a cell-free ass… | 1 mg | 38874-1 | More Info |
| TG2-179-1 | A BAP1 inhibitor; inhibits BAP1 deubiquitinase activity in a cell-free ass… | 10 mg | 38874-10 | More Info |
| TG2-179-1 | A BAP1 inhibitor; inhibits BAP1 deubiquitinase activity in a cell-free ass… | 5 mg | 38874-5 | More Info |
| TG4-155 | A selective, brain penetrant EP2 antagonist (KB = 2.4 nM); blocks the indu… | 10 mg | 17639-10 | More Info |
| TG4-155 | A selective, brain penetrant EP2 antagonist (KB = 2.4 nM); blocks the indu… | 25 mg | 17639-25 | More Info |
| TG4-155 | A selective, brain penetrant EP2 antagonist (KB = 2.4 nM); blocks the indu… | 5 mg | 17639-5 | More Info |
| TG4-155 | A selective, brain penetrant EP2 antagonist (KB = 2.4 nM); blocks the indu… | 50 mg | 17639-50 | More Info |
| TG6-10-1 | A potent EP2 receptor antagonist (Kb = 17.8 nM in C6 glioma cells overexpr… | 1 mg | 23444-1 | More Info |
| TG6-10-1 | A potent EP2 receptor antagonist (Kb = 17.8 nM in C6 glioma cells overexpr… | 10 mg | 23444-10 | More Info |
| TG6-10-1 | A potent EP2 receptor antagonist (Kb = 17.8 nM in C6 glioma cells overexpr… | 25 mg | 23444-25 | More Info |
| TG6-10-1 | A potent EP2 receptor antagonist (Kb = 17.8 nM in C6 glioma cells overexpr… | 5 mg | 23444-5 | More Info |
| TG6-129 | A selective antagonist of the EP2 receptor, suppressing PGE2-induced eleva… | 1 mg | 19085-1 | More Info |
| TG6-129 | A selective antagonist of the EP2 receptor, suppressing PGE2-induced eleva… | 5 mg | 19085-5 | More Info |
| TG6-129 | A selective antagonist of the EP2 receptor, suppressing PGE2-induced eleva… | 500 µg | 19085-500 | More Info |
| TG11-77 (hydrochloride) | An EP2 receptor antagonist (KB = 9.7 nM); selective for EP2 over DP1, EP4,… | 1 mg | 30188-1 | More Info |
| TG11-77 (hydrochloride) | An EP2 receptor antagonist (KB = 9.7 nM); selective for EP2 over DP1, EP4,… | 10 mg | 30188-10 | More Info |
| TG11-77 (hydrochloride) | An EP2 receptor antagonist (KB = 9.7 nM); selective for EP2 over DP1, EP4,… | 5 mg | 30188-5 | More Info |
| TGN 020 | An AQP4 inhibitor (IC50 = 3.1 µM in X. laevis oocytes transfected wi… | 10 mg | 30955-10 | More Info |
| TGN 020 | An AQP4 inhibitor (IC50 = 3.1 µM in X. laevis oocytes transfected wi… | 100 mg | 30955-100 | More Info |
| TGN 020 | An AQP4 inhibitor (IC50 = 3.1 µM in X. laevis oocytes transfected wi… | 25 mg | 30955-25 | More Info |
| TGN 020 | An AQP4 inhibitor (IC50 = 3.1 µM in X. laevis oocytes transfected wi… | 50 mg | 30955-50 | More Info |
| TGR-1202 | A PI3K p110δ inhibitor (IC50 = 22 nM); selective for p110δ ove… | 100 mg | 32877-100 | More Info |
| TGR-1202 | A PI3K p110δ inhibitor (IC50 = 22 nM); selective for p110δ ove… | 25 mg | 32877-25 | More Info |
| TGR-1202 | A PI3K p110δ inhibitor (IC50 = 22 nM); selective for p110δ ove… | 5 mg | 32877-5 | More Info |
| TGR-1202 | A PI3K p110δ inhibitor (IC50 = 22 nM); selective for p110δ ove… | 50 mg | 32877-50 | More Info |
| TGR5 (GP-BAR1) Reporter Assay Kit | Cayman's TGR5 (GP-BAR1) Reporter Assay Kit consists of a 96-well plate coa… | 1 ea | 601440-96WELLS | More Info |
| TGR5 Receptor Agonist | An agonist of the bile acid G protein-coupled receptor TGR5 (EC50s = 31.6-… | 1 mg | 16291-1 | More Info |
| TGR5 Receptor Agonist | An agonist of the bile acid G protein-coupled receptor TGR5 (EC50s = 31.6-… | 10 mg | 16291-10 | More Info |
| TGR5 Receptor Agonist | An agonist of the bile acid G protein-coupled receptor TGR5 (EC50s = 31.6-… | 25 mg | 16291-25 | More Info |
| TGR5 Receptor Agonist | An agonist of the bile acid G protein-coupled receptor TGR5 (EC50s = 31.6-… | 5 mg | 16291-5 | More Info |
| TGX-221 | A potent, selective, and cell permable inhibitor of PI3K p110b; IC50 value… | 1 mg | 10007349-1 | More Info |
| TGX-221 | A potent, selective, and cell permable inhibitor of PI3K p110b; IC50 value… | 10 mg | 10007349-10 | More Info |
| TGX-221 | A potent, selective, and cell permable inhibitor of PI3K p110b; IC50 value… | 5 mg | 10007349-5 | More Info |
| TGX-221 | A potent, selective, and cell permable inhibitor of PI3K p110b; IC50 value… | 500 µg | 10007349-500 | More Info |
| TH1020 | An inhibitor of the TLR5-flagellin protein-protein interaction; disrupts T… | 10 mg | 33553-10 | More Info |
| TH1020 | An inhibitor of the TLR5-flagellin protein-protein interaction; disrupts T… | 25 mg | 33553-25 | More Info |
| TH1020 | An inhibitor of the TLR5-flagellin protein-protein interaction; disrupts T… | 5 mg | 33553-5 | More Info |
| TH1020 | An inhibitor of the TLR5-flagellin protein-protein interaction; disrupts T… | 50 mg | 33553-50 | More Info |
| TH257 | An inhibitor of LIMK1 and LIMK2 (IC50s = 84 and 39 nM, respectively) | 10 mg | 34236-10 | More Info |
| TH257 | An inhibitor of LIMK1 and LIMK2 (IC50s = 84 and 39 nM, respectively) | 25 mg | 34236-25 | More Info |
| TH257 | An inhibitor of LIMK1 and LIMK2 (IC50s = 84 and 39 nM, respectively) | 5 mg | 34236-5 | More Info |
| TH257 | An inhibitor of LIMK1 and LIMK2 (IC50s = 84 and 39 nM, respectively) | 50 mg | 34236-50 | More Info |
| TH263 | An inactive analog of TH257; has been used as a negative control for the k… | 10 mg | 37295-10 | More Info |
| TH263 | An inactive analog of TH257; has been used as a negative control for the k… | 25 mg | 37295-25 | More Info |
| TH263 | An inactive analog of TH257; has been used as a negative control for the k… | 5 mg | 37295-5 | More Info |
| TH263 | An inactive analog of TH257; has been used as a negative control for the k… | 50 mg | 37295-50 | More Info |
| TH287 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 1 mg | 18132-1 | More Info |
| TH287 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 10 mg | 18132-10 | More Info |
| TH287 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 5 mg | 18132-5 | More Info |
| TH-302 | A hypoxia-activated prodrug and DNA alkylating agent with anticancer activ… | 1 mg | 22195-1 | More Info |
| TH-302 | A hypoxia-activated prodrug and DNA alkylating agent with anticancer activ… | 10 mg | 22195-10 | More Info |
| TH-302 | A hypoxia-activated prodrug and DNA alkylating agent with anticancer activ… | 25 mg | 22195-25 | More Info |
| TH-302 | A hypoxia-activated prodrug and DNA alkylating agent with anticancer activ… | 5 mg | 22195-5 | More Info |
| TH588 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 1 mg | 18133-1 | More Info |
| TH588 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 10 mg | 18133-10 | More Info |
| TH588 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 25 mg | 18133-25 | More Info |
| TH588 | A selective inhibitor of the nucleotide pool sanitizing enzyme MTH1 (IC50… | 5 mg | 18133-5 | More Info |
| TH-1760 | A NUDT15 inhibitor (IC50 = 25 nM); selective for NUDT15 over a panel of ad… | 10 mg | 40469-10 | More Info |
| TH-1760 | A NUDT15 inhibitor (IC50 = 25 nM); selective for NUDT15 over a panel of ad… | 25 mg | 40469-25 | More Info |
| TH-1760 | A NUDT15 inhibitor (IC50 = 25 nM); selective for NUDT15 over a panel of ad… | 5 mg | 40469-5 | More Info |
| TH-1760 | A NUDT15 inhibitor (IC50 = 25 nM); selective for NUDT15 over a panel of ad… | 50 mg | 40469-50 | 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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