| 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 |
| M57256 | PM102 | PM102 (HepArrest) is a heparin antagonist that can reverses the anticoagulant effect of heparin. |
| M57255 | CRSP-1 | CRSP-1 is short for calcitonin receptor-stimulating peptide-1. |
| M57254 | ARN14686 | ARN14686 is an activity-based protein profiling (ABPP) probe. |
| M57243 | S07662 | S07662 is a human constitutive androstane receptor (hCAR) inhibitor with an IC50 of 0.7 μM. |
| M57065 | Sm4 | Sm4 is a SOX18 inhibitor. |
| M57064 | YMU1 | YMU1 is a selective inhibitor of human thymidylate kinase (hTMPK) with an IC50 of 610 nM. |
| M57063 | BNN3 | BNN3 is a caged nitric oxide (NO) donor. |
| M57062 | Ap3A | Ap3A is a vasoactive molecule. |
| M57061 | BMPO | BMPO (BocMPO) is a cell-permeable superior spin trap with favorable chemical and spectroscopic features. |
| M57059 | FL104 | FL104 is a potent small molecule urotensin II receptor agonist with pEC50 of 7.11 for UTII receptor in R-SATTM assay. |
| M57056 | X5050 | X5050 is a REST inhibitor, with an EC50 of 2.1 μM. |
| M57055 | ZT-1a | ZT-1a is a potent, non-ATP-competitive and selective SPAK inhibitor. |
| M57054 | ML179 | ML179 (SR-1309) is a inverse LRH1 (Liver receptor homologue-1) agonist with IC50 of 320 nM. |
| M57053 | HOPan | HoPan inhibits phosphopantotenoylcysteine synthetase activity. |
| M57052 | IND24 | IND24 is a potent antiprion agent with an EC50 value of 1.27 µM. |
| M57051 | MKI-1 | MKI-1, an inhibitor of MASTL (microtubule-associated serine/threonine kinase-like) with an IC50 of 9.9 μM, exerts antitumor and radiosensitizer activities through PP2A activation in breast cancer. |
| M57050 | CIL62 | CIL62 is a caspase-3/7-independent cell death inducer. |
| M57049 | ML095 | ML095 is a biochemical inhibitor of PLAP. |
| M57048 | Valnivudine hydrochloride | FV-100 is a potent, selective and orally active anti-varicella zoster virus agent. |
| M57047 | GPi688 | GPi688 is a potent and orally active glycogen phosphorylase (GPa) inhibitor with IC50s of 19 nM, 61 nM and 12 nM for human liver GPa, rat liver GPa and human skeletal muscle GPa, respectively. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
