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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
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.
M8163 Spermine tetrahydrochloride Mixed NMDA agonist/antagonist at the polyamine site.
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.
M8153 N-Methylspiperone hydrochloride D2 dopamine receptor antagonist.
M8152 ST638 Protein tyrosine kinase inhibitor (IC50 = 370 nM).
M8150 SB-668875 SB-668875 is a novel, selective peptide agonist at OX2 orexin receptors.
M8148 LY-165,163 Selective 5-HT1A serotonin receptor agonist and 5-HT1D serotonin receptor antagonist.




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