| 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 |
| M6847 | JNJ 27141491 | JNJ 27141491 is a potent and selective human CCR2 antagonist. |
| M6845 | JNJ 10397049 | JNJ 10397049 is a selective OX 2 receptor antagonist. |
| M6842 | JH 295 | JH 295 is a irreversible Nek2 inhibitor. |
| M6840 | J 113863 | J 113863 is a potent CCR1 chemokine receptor antagonist. |
| M6838 | IT 901 | IT 901 is a nF-κB c-Rel subunit inhibitor. |
| M6837 | Isamoltane hemifumarate | Isamoltane hemifumarate is a 5-HT 1B antagonist. |
| M6836 | Irsogladine maleate | Irsogladine maleate is a pDE4 inhibitor; antiulcer agent. |
| M6832 | IP7e | IP7e is a potent Nurr1 activator. |
| M6829 | INDY | INDY is a dYRK1A/B inhibitor. |
| M6828 | Indiplon | Indiplon is a subtype-selective GABA A receptor positive allosteric modulator. |
| M6827 | Indibulin | Indibulin is a microtubule destabilizer. |
| M6825 | Impentamine dihydrobromide | Impentamine dihydrobromide is a selective H 3 antagonist. |
| M6824 | Imiloxan hydrochloride | Imiloxan hydrochloride is a highly selective α 2B antagonist. |
| M6822 | iMAC2 | iMAC2 is a suppressor of mitochondrial apoptosis. |
| M6819 | IHR 1 | IHR 1 is a potent Smo antagonist. |
| M6818 | Ifenprodil hemitartrate | Ifenprodil hemitartrate is a non-competitive NMDA antagonist. Also σ ligand. |
| M6817 | IEM 1460 | IEM 1460 is a open-channel blocker of AMPA currents; selective for non-GluR2-containing receptors. |
| M6816 | IDRA 21 | IDRA 21 is a inhibits AMPA receptor desensitization. |
| M6815 | IDE 2 | IDE 2 is a induces definitive endoderm formation in mouse and human ESCs. |
| M6812 | ICI 89406 | ICI 89406 is a β antagonist. |
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