| 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 |
| M6761 | GR 135531 | GR 135531 is a high affinity melatonin MT 3 ligand. |
| M6758 | GP 1a | GP 1a is a cB 2 receptor inverse agonist. |
| M6757 | GNTI dihydrochloride | GNTI dihydrochloride is a potent, selective κ antagonist. |
| M6745 | Gavestinel | Gavestinel is a potent and selective glycine site antagonist; orally available and active in vivo. |
| M6742 | Galiellalactone | Galiellalactone is a sTAT3 inhibitor; active in vivo. |
| M6738 | G 28UCM | G 28UCM is a fASN inhibitor. |
| M6736 | FR 236924 | FR 236924 is a selective PKCε activator. |
| M6729 | FGIN-1-27 | FGIN-1-27 is a potent, specific ligand for mitochondrial DBI receptor. |
| M6726 | FERb 033 | FERb 033 is a potent and selective ERβ agonist. |
| M6724 | Fenoldopam hydrochloride | Fenoldopam hydrochloride is a selective D 1-like partial agonist. |
| M6722 | Fenobam | Fenobam is a potent and selective mGlu 5 antagonist. |
| M6721 | ETP 45658 | ETP 45658 is a potent PI 3-kinase inhibitor; also inhibits DNA-PK and mTOR. |
| M6719 | Eticlopride hydrochloride | Eticlopride hydrochloride is a selective D 2/D 3 Antipsychotic compounds. |
| M6716 | ER 819762 | ER 819762 is a potent EP 4 receptor antagonist; orally bioavailable. |
| M6715 | ER 27319 maleate | ER 27319 maleate is a selective Syk kinase inhibitor. |
| M6713 | Eplivanserin hemifumarate | Eplivanserin hemifumarate is a potent and selective 5-HT 2A antagonist. |
| M6712 | EO 1428 | EO 1428 is a selective inhibitor of p38α and p38β 2. |
| M6711 | Enoximone | Enoximone is a pDE3 inhibitor. |
| M6709 | EMD 66684 | EMD 66684 is a potent, selective non-peptide AT 1 antagonist. |
| M6708 | EMD 386088 hydrochloride | EMD 386088 hydrochloride is a potent 5-HT 6 agonist. |
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