| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M8339 | Cardionogen-2 | Cardionogen-2 is a biphasic modulator of cardiogenesis that enlarges the size of the zebrafish embryonic heart by promoting cardiomyocyte formation. |
| M8338 | NPD4456 | NPD4456 is an HIV-1 Vpr inhibitor that directly binds to HIV-1 Vpr. |
| M8337 | ST247 | ST247 is a PPAR β/δ selective inverse agonist. |
| M8334 | FQI1 | FQI1 inhibits the DNA-binding activity of LSF, a ubiquitous transcription factor that is up regulated in many hepatocellular carcinomas (HCC). |
| M8333 | IM-54 | IM-54 is a cell permeable, potent and selective inhibitor of necrosis. |
| M8332 | PT-S58 | PT-S58 is a PPAR β/δ full antagonist, and a derivative of GSK0660. |
| M8330 | Carboxyamidotriazole | Carboxyamidotriazole (L-651582) is an orally active calcium channel blocker. |
| M8328 | RBx-0597 | RBx-0597 is a potent, competitive inhibitor of DPP-IV (IC50 = 30 nM), that displays selectivity or 150 and 300 fold over DDP-VIII and DDP-IX, respectively. |
| M8326 | Salsolinol hydrobromide | Salsolinol is the condensation product of acetaldehyde and dopamine. |
| M8325 | DR2313 | DR2313 is a PARP-1; PARP-2 inhibitor (Ki = 0. |
| M8320 | CUR61414 | CUR61414 specifically binds to, and antagonizes the activity of smoothened (Smo) in the hedgehog signaling pathway. |
| M8319 | Eicosapentaenoyl ethanolamide | Eicosapentaenoyl ethanolamide (EPEA) is a lipid mediator that has been found to suppress lifespan extension resulting from dietary restriction in C. |
| M8317 | ALLO-1 | ALLO-1 is a Smoothened (Smo) antagonist that inhibits both wild-type and mutant Smo, including D473H SMO mutant. |
| M8316 | FMP-API-1 | FMP-API-1 is an inhibitor of AKAP-PKA interactions in vitro and in cultured cardiac myocytes that activates PKA. |
| M8315 | Ralfinamide mesylate | Ralfinamide is a mixed sodium and N-type calcium channel blocker. |
| M8314 | CGS 9895 | CGS 9895 is a GABA antagonist that acts via the benzodiazepine binding site of ag containing GABA receptors. |
| M8312 | NSC23925 | NSC23925 is a specific Pgp1 inhibitor. |
| M8310 | CHD-5 | CHD-5 is a potent aryl hydrocarbon receptor antagonist. |
| M8309 | VK3-OCH3 | VK3-OCH3 is an analog of Vitamin K3 (Menadione) with potent antitumor activity. |
| M8308 | Cipamfylline | Cipamfylline is a PDE4 inhibitor that has been shown to cause a cellular redistribution of PDE4A4 into accretion foci, through an association with the ubiquitin scaffolding protein p62. |
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