| 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 |
| M7352 | Talsupram hydrochloride | Talsupram hydrochloride is a selective inhibitor of noradrenalin transporters. |
| M7349 | TAK 21d | TAK 21d is a potent FAAH inhibitor. |
| M7348 | TACA | TACA is a gABA A agonist. Also GABA-T substrate and GABA uptake inhibitor. |
| M7347 | Tabimorelin hemifumarate | Tabimorelin hemifumarate is a potent, orally active ghrelin receptor agonist. |
| M7345 | T 98475 | T 98475 is a gnRH receptor antagonist. |
| M7344 | T 5601640 | T 5601640 is a selective LIMK2 inhibitor; antitumor. |
| M7338 | Sulfidefluor 7 AM | Sulfidefluor 7 AM is a h 2S fluorescent probe. |
| M7337 | STOCK2S 26016 | STOCK2S 26016 is a lysine deficient protein kinase (WNK) signaling inhibitor. |
| M7335 | STEARDA | STEARDA is a endogenous lipid, active in vivo. Enhances effects of endovanilloids at TRPV1 receptors. |
| M7334 | ST 1936 oxalate | ST 1936 oxalate is a selective, high affinity 5-HT 6 agonist. |
| M7333 | SSR 69071 | SSR 69071 is a potent, orally active human leukocyte elastase inhibitor. |
| M7332 | SR 7826 | SR 7826 is a potent and selective LIMK inhibitor; antitumor. |
| M7331 | SR 57227 hydrochloride | SR 57227 hydrochloride is a potent, selective 5-HT 3 agonist. |
| M7329 | SR 3576 | SR 3576 is a highly potent and selective JNK3 inhibitor. |
| M7328 | SR 33805 oxalate | SR 33805 oxalate is a ca 2+ channel blocker; binds allosterically to distinct site on L-type channels. |
| M7326 | SR 142948 | SR 142948 is a highly potent NT receptor antagonist. |
| M7324 | SR 12813 | SR 12813 is a pregnane X receptor agonist. |
| M7320 | Spiperone hydrochloride | Spiperone hydrochloride is a 5-HT 2A antagonist. Also D 2-like antagonist. |
| M7313 | SN 2 | SN 2 is a selective TRPML3 channel activator. |
| M7311 | SMBA 1 | SMBA 1 is a high affinity and selective activator of Bax. |
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