| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M8190 | Sorbinil | Sorbinil decreases the level of sorbitol in red blood cells and increases the velocity of nerve conduction. |
| M8185 | Strophanthidin | Strophanthidin is a cardiotonic steroid that elevates the activity of Na+/K+-ATPase in cardiac myocytes. |
| M8183 | Suptopin-2 | Sutopin-2 is a suppressor of topoisomerase II inhibition. |
| M8182 | SG-209 | Potassium channel activator; analog of nicorandil; nitrate-free coronary vasodilator. |
| M8181 | SW02 | SW02 is a specific activator/agonist of Hsp70. |
| M8180 | S-15176 difumarate salt | Antioxidant and anti-ischemic agent. |
| M8179 | SYUIQ-5 | SYUIQ-5 is a Cryptolepine derivative, which induces and stabilizes G-quadruplexes. |
| M8177 | SB-271046A | The first potent and selective 5-HT6 antagonist. |
| M8176 | S15535 | Potent, orally active, partial 5-HT1A receptor agonist. |
| M8175 | SF-22 | Radioligand studies reveal that SF-22 also targets 5-HT2B and 5-HT6 serotonin receptors and dopamine transporter. |
| M8174 | SFK1 | SFK1 interacts directly with yeast mitochodria. |
| M8171 | SID 852843 | SID 852843 is an inhibitor of West Nile Virus NS2B-NS3 proteinase. |
| M8167 | SB-204070 hydrochloride | Selective 5-HT4 serotonin receptor antagonist. |
| M8166 | Sulindac sulfide | Sulindac sulfide is a non-steroidal anti-inflammatory compound with a preference for COX-1; it is an inhibitor of Ras activation of Raf-1. |
| M8165 | SC 19220 | EP1 Prostanoid receptor antagonist. |
| M8162 | SKF-83959 hydrobromide | D1 dopamine receptor agonist. |
| M8161 | SE 175 | An organic nitrate compound that acts as an NO donor in vivo following reductive transformation of the nitrate group to nitric oxide. |
| M8158 | SDZ-205,557 hydrochloride | Potent, selective 5-HT4 serotonin receptor antagonist. |
| M8157 | Sordarin sodium salt | Sordarin is an antifungal metabolite possessing a tetracyclic diterpene glycoside structure. |
| M8155 | SID7969543 | SID7969543 is a SF-1 (or NR5A1) inhibitor. |
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