| 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 |
| M8252 | JFD01307SC | JFD01307SC is a glutamine synthase inhibitor and antituberculous compound. |
| M8231 | Perhexiline maleate salt | Perhexiline maleate is an anti-anginal metabolic modulator. |
| M8222 | Acenocoumarol | Acenocoumarol is a warfarin analog, an anticoagulant that inhibits Vitamin K epoxide reductase. |
| M8221 | Trapidil | Terapidil is an antiplatelet compound that partially acts as a competitive inhibitor of phosphodiesterase inhibitors and platelet-derived growth factor (PDGF) receptors. |
| M8217 | BLT-1 | Block lipid transport-1 (BLT-1) is a specific inhibitor of the SR-BI (Scavenger receptor, class B, type I) mediated lipid transfer. |
| M8201 | Sesamin | Non-competitive Δ5-desaturase inhibitor. |
| M8187 | SB 657510 | SB 657510 slows development of diabetes-associated atherosclerosis in mouse model of diabetes. |
| M8164 | Stauprimide | Stauprimide is an enhancer stem cell differentiation into endoderm. |
| M8159 | STX64 | STX64 is a potent, irreversible inhibitor of steroid sulfatase. |
| M8151 | SR-95531 | SR-95531 is a specific GABAA receptor antagonist that does not affect GABA-transaminase or glutamate-decarboxylase activities. |
| M8130 | Ro 41-0960 | Ro 41-0960 is a selective catechol-O-methyltransferase(COMT) inhibitor. |
| M8129 | RN-1747 | TRPV4, a close relative of the vanilloid receptor TRPV1, is activated by diverse modalities such as endogenous lipid ligands, hypotonicity, protein kinases and, possibly, mechanical inputs. |
| M8123 | Quinidine sulfate salt dihydrate | Class IA antiarrhythmic; potassium channel blocker. |
| M8122 | PF-06456384 trihydrochloride | PF-06456384 is a highly potent and selective inhibitor against voltage-gated sodium channel NaV1. |
| M8103 | CP724714 | CP724714 is a potent and selective inhibitor of HER2/ErbB2 with an IC50 value of 10 nM. |
| M8043 | PD-161570 | PD-161570 is an inhibitor of human FGF-1 receptor tyrosine kinase. |
| M8042 | CP-335963 | CP-335963 is an aurora 2 kinase inhibitor, PDGF inhibitor, and anti-proliferative. |
| M8034 | Dofetilide | Dofetilide is a Class III antiarrhythmic and hERG channel blocker. |
| M8000 | Pirenperone | 5-HT2 serotonin receptor antagonist. |
| M7996 | PRL-3 Inhibitor I | PRL-3 Inhibitor I is a rhodanine derivative with an IC50 value of 0. |
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