| 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 |
| M6884 | L-732,138 | L-732,138 is a potent, selective NK 1 antagonist. |
| M6883 | L-694,247 | L-694,247 is a 5-HT 1D agonist. |
| M6882 | L-690,488 | L-690,488 is a cell permeable prodrug of the IMPase inhibitor L-690,330. |
| M6880 | L-689,560 | L-689,560 is a very potent NMDA antagonist. |
| M6878 | L-168,049 | L-168,049 is a potent, orally active human glucagon receptor antagonist. |
| M6877 | L-165,041 | L-165,041 is a potent PPARδ agonist. |
| M6873 | KW 3902 | KW 3902 is a selective A 1 antagonist. |
| M6871 | KRCA 0008 | KRCA 0008 is a potent Ack1 and ALK dual inhibitor; orally bioavailable. |
| M6862 | K-252c | K-252c is a protein kinase C inhibitor. |
| M6861 | K 114 | K 114 is a amyloid fibril-specific fluorescent dye. |
| M6860 | JZP 430 | JZP 430 is a potent and irreversible α/β-hydrolase domain 6 (ABHD6) inhibitor. |
| M6859 | JZP 361 | JZP 361 is a potent and selective reversible MAGL inhibitor. |
| M6858 | JX 401 | JX 401 is a potent, reversible p38α inhibitor. |
| 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. |
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