| 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 |
| M8282 | Deformylflustrabromine hydrochloride | Desformylflustrabromine (dFBr) is a potent, selective positive allosteric modulator of α4β2 nicotinic receptor; increases efficacy and potency of acetylcholine. |
| M8280 | PSNCBAM-1 | PSNCBAM-1 is an allosteric, non-competitive antagonist of CB-1. |
| M8279 | ABL127 | ABL127 is a potent and selective inhibitor of Protein phosphatase methylesterase-1 (PME-1 or PPME-1). |
| M8278 | MLS000389544 | MLS000389544 is a selective and potent methylsulfonylnitrobenzoa |
| M8275 | LG100268 | LG100268 (LG268) is a potent and selective rexinoid and retinoid-X receptor (RXR) agonist. |
| M8273 | NSC 162535 disodium salt | NSC 162535 is an inhibitor of RNA editing in trypanosomatid pathogens that results from lost of the interaction of core editosome with substrate RNA. |
| M8271 | GSK575594A | GSK575594A is a selective agonist of human GPR55. |
| M8270 | 2OHOA | 2OHOA induces cell cycle arrest and apoptosis in several cancer cell lines, including glioma, leukemia, breast and colon cancer lines. |
| M8268 | 4-MDM | 4-MDM augments the aminopeptidase activity of LTA4 hydrolase without affecting the conversion of LTA4 to LTB4. |
| M8267 | Anisodamine | Anisodamine is a muscarinic receptor antagonist. |
| M8266 | ML169 | ML169 is a positive allosteric modulator (PAM) of the muscurinic acetycholine receptor M1 (CHRM1). |
| M8263 | LY255582 | LY255582 inhibits the diet-associated increases in mesolimbic dopamine levels and reduces the consumption of highly-palatable food intake. |
| M8256 | EAA-090 | EAA-090 inhibits the binding of ligands to glutamate receptors and blocks NMDA-induced currents. |
| M8253 | Mifamurtide | Mifamurtide (Muramyl tripeptide phosphatidylethanolamine; MTP-cephalin; MTP-PE) is a synthetic, lipophilic analog of muramyl dipeptide. |
| M8252 | JFD01307SC | JFD01307SC is a glutamine synthase inhibitor and antituberculous compound. |
| M8251 | CJ-13610 | CJ-13,610 is a potent inhbititor of 5-lipoxygenase (5-LO) activity (IC50 = 70 nM). |
| M8250 | Dp44mT | Dp44mT is an iron chelator that works as a selective anticancer agent. |
| M8249 | EM20-25 | EM20-25 disrupts the BCL-2/BAX interactions and activates caspase-9 in cells overexpressing BCL-2. |
| M8248 | S 17092 | S-17092 is a potent, selective inhibitor of Prolyl oligopeptidase (POP), also known as prolyl endopeptidase (PEP or PE). |
| M8246 | GPR35 Agonist, Compound 10 | GPR35 agonist Compound 10 is a GPR35 agonist the binds with higher affinity than other known agonists, such as kynurenic acid and zaprinast. |
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