| 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 |
| 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. |
| M8147 | RX 821002 hydrochloride | Selective α2-adrenoceptor antagonist. |
| M8145 | Ro4368554 | Ro4368554 is a 5-HT6 receptor antagonist. |
| M8143 | Razoxane | Razoxane is clinically active against angiogenesis and metastasis. |
| M8142 | RRD-251 hydrochloride | RRD-251 hydrochloride is a reversible, potent, and selective disruptor of Rb/Raf-1 interaction. |
| M8140 | REV 5901 | Leukotriene D4 receptor antagonist. |
| M8139 | Ridaifen-B | Ridaifen-B (RID-B) is a novel tamoxifen (TAM) analog that significantly augments apoptosis-inducing effect of TAM in estrogen receptor (ER)-negatives cells. |
| M8138 | RU 26752 | RU 26752 is a mineralocorticoid receptor antagonist. |
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