| 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 |
| M7594 | AH 11110 | α1B-adrenoceptor ligand. |
| M7593 | ATPA | Selective kainate receptor agonist. |
| M7592 | 5α-Androstan-3β-ol | mCAR (constitutive androstane receptor) inverse agonist; testosterone metabolite. |
| M7589 | Arecaidine propargyl ester hydrobromide | Potent muscarinic acetylcholine receptor agonist exhibiting slight selectivity for M2 receptors; inactive at nicotinic receptors. |
| M7586 | AC-7954 | Nonpeptide GPR14 / urotensin-UII (UII) receptor agonist that has an EC50 of 300 nM at the human UII receptor (h-UTR). |
| M7503 | YM 511 | YM 511 is a potent aromatase (CYP19) inhibitor. |
| M7502 | YM 298198 hydrochloride | YM 298198 hydrochloride is a highly potent, selective non-competitive mGlu 1 antagonist. |
| M7501 | YM 022 | YM 022 is a highly potent, selective non-peptide CCK 2 antagonist. |
| M7499 | YE 120 | YE 120 is a gPR35 agonist. |
| M7498 | Y-26763 | Y-26763 is a k ir6 (K ATP) channel opener. |
| M7497 | Y 11 | Y 11 is a potent and selective FAK inhibitor. |
| M7496 | XRP44X | XRP44X is a ras-Net pathway inhibitor. |
| M7494 | XE 991 dihydrochloride | XE 991 dihydrochloride is a potent, selective K V7 (KCNQ) channel blocker; blocks M-currents. |
| M7492 | XAP 044 | XAP 044 is a potent and selective mGlu 7 antagonist. |
| M7491 | WR 1065 | WR 1065 is a p53 activator. Also ROS scavenger. |
| M7488 | WIN 64338 hydrochloride | WIN 64338 hydrochloride is a bradykinin B 2 antagonist. |
| M7485 | WAY 208466 dihydrochloride | WAY 208466 dihydrochloride is a selective 5-HT 6 agonist. |
| M7484 | WAY 207024 dihydrochloride | WAY 207024 dihydrochloride is a gnRH receptor antagonist. |
| M7482 | WAY 181187 oxalate | WAY 181187 oxalate is a high affinity and selective 5-HT 6 agonist. |
| M7480 | W-5 hydrochloride | W-5 hydrochloride is a calmodulin antagonist. |
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