| 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 |
| M8839 | U-74389G | Free radical lipid peroxidation inhibitor in cultured brain cells, monocytic THP1 cells, and LLC-PK1 cell layers. |
| M8835 | UA62784 | Studies have also reported that UA62784 associates with tubulin at or near the colchicine-binding sites in cells and functions as a cytotoxic, microtubule inhibitor. |
| M8834 | U-62066 | Highly selective κ opioid receptor agonist; antitussive. |
| M8831 | 5-Methylurapidil | Selective α1A-adrenoceptor antagonist; antihypertensive. |
| M8828 | Tofisopam | Ligand for the GABAA receptor benzodiazepine modulatory site. |
| M8827 | Tyrphostin 51 | Tyrphostin 51 is an EGFR tyrosine kinase inhibitor. |
| M8826 | TN-16 | Inhibitor of microtubule assembly. |
| M8817 | THI | 2-Acetyl-4-tetrahydroxybu |
| M8816 | TPh A | TPh A is an inhibitor of the nuclear protein pirin. |
| M8814 | Trap-101 hydrochloride | Trap-101 Hydrochloride is a nociceptin/orphanin FQ peptide (NOP) receptor blocker. |
| M8813 | Tyrphostin AG 825 | EGF receptor tyrosine kinase inhibitor, inactive against IGF-1 Receptor. |
| M8812 | TPBM | TPBM is a potent inhibitor of estrogen receptor α via blocking ERα binding to consensus estrogen response element (cERE) DNA. |
| M8810 | Taprostene sodium salt | Highly selective IP1 prostanoid receptor agonist. |
| M8809 | Trandolapril | Studies have reported that trandolapril inhibits atherosclerosis1 and decreases the occurrence of atrial fibrillation2. |
| M8808 | Terodiline hydrochloride | Terodiline is known to increase corrected QT interval (QTc) and decrease resting heart rate in elderly patients. |
| M8805 | Terameprocol | Terameprocol is a synthetic derivative of NDGA, a non-selective lipoxygenase inhibitor. |
| M8801 | TIQ-A | TIQ-A is a potent inhibitor of PARP, anti-apoptotic. |
| M8800 | T3MG | T3MG is a selective inhibitor of excitatory amino acid transporters GLT-1, EAAT2, and EAAT4. |
| M8799 | Talsaclidine | Talsaclidine is a M1 selective muscarinic receptor agonist. |
| M8797 | (+)-Thalidomide | (-)-Thalidomide selectively inhibits biosynthesis of tumor necrosis factor α (TNF-α). |
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