| 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 |
| M8206 | PDI inhibitor 16F16 | 16F16 is a protein disulfide isomerase (PDI) inhibitor, first identified in a screen for compounds that prevent apoptosis induced by mutant huntingtin protein. |
| M8205 | SR 142948A | SR 142948A is a non-peptide Neurotensin receptor antagonist. |
| M8204 | VAHA | Hydroxamic acid derivatives of valproic acid exhibit anticonvulsant activity with no teratogenic activity in mouse neural tube defect model. |
| M8200 | SB 220025 trihydrochloride | SB 220025 is a potent, specific inhibitor of human p38 mitogen-activated protein (MAP) kinase, with an IC50 value of 60 nM and 50- to 1000-fold selectivity. |
| M8198 | Sulprostone | Selective EP3 prostanoid receptor agonist. |
| M8194 | SKI 5C | SKI 5C is a selective Sphingosine Kinase 1 (SPHK1) inhibitor. |
| M8192 | SJ000025081 | SJ000025081 is a dihydropyridine effective against Plasmodium yoelii. |
| M8191 | Salvinorin A | Salvinorin A is a potent, non-nitrogenous κ opioid selective receptor agonist. |
| 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. |
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