| 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 prevent 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. |
| M9331 | 10-Hydroxy-trans-2-decenoic acid | 10-hydroxy-2-decenoic acid (10-H2DA) is the principal lipid component in royal jelly which is the food for queen and larvae honeybees. |
| M7985 | Olprinone hydrochloride | Selective phosphodiesterase 3 (PDE3) inhibitor. |
| M7984 | Opipramol dihydrochloride | σ1/σ2 opioid receptor agonist; an antagonist at D2, 5HT2 and H1 receptors; atypical antidepressant, antipsychotic and anxiolytic. |
| M7983 | 9,12-Octadecadiynoic acid | Potent cyclooxygenase and lipoxygenase inhibitor. |
| M7981 | Oxamflatin | Histone deacetylase inhibitor; anti-cancer agent. |
| M7980 | Ouabain octahydrate | Cardiac glycoside, inhibits Na(+)/K(+) ATPase, regulates transcription of MDR (increase, Pgp) and MRP (increase MRP1 and decrease CFTR, cyctic fibrosis transport receptor or cAMP-activated Cl- channel) genes, also alters localization of MRP1. |
| M7978 | OPC 31260 hydrochloride | OPC 31260 is a vasopressin V2 selective antagonist. |
| M7977 | Octoclothepin maleate salt | Octoclothepin maleate salt is a D2 dopamine receptor antagonist; 5-HT2 serotonin receptor antagonist. |
| M7976 | Oxotremorine M | Nonselective muscarinic acetylcholine receptor agonist. |
| M7974 | Netropsin dihydrochloride | Netropsin is an unusual n-methylpyrrole-containin |
| M7973 | NSC 295642 | NSC 295642 is a potent inhibitor of cell migration. |
| M7972 | NSC308848 | NSC308848 is a small molecular transcription factor inhibitor. |
| M7971 | NSC727447 | NSC727447 is an inhibitor of ribonuclease H (Rnase H) of HIV-1 and HIV-2. |
| M7970 | NIDA-41020 | NIDA-41020 is a CB1 cannabinoid receptor antagonist. |
| M7969 | NS3694 | NS3694 is an Inhibitor of apoptosome formation. |
| M7968 | 7-Nitroindazole | Selective inhibitor of nitric oxide synthase from mouse brain. |
| M7967 | NN-DNJ | Nn-dnj is a glucosidase inhibitor that acts as a compound chaperone. |
| M7966 | Norharmane | Inhibitor of indoleamine 2,3-dioxygenase (IDO). |
| M7965 | Neridronate | Neridronate is a bone resorption inhibitor. |
| M7962 | NBI 27914 | NBI 27914 is a CRF1 corticotropin-releasing factor receptor antagonist. |
| M7957 | (+)-Norfenfluramine hydrochloride | (+)-Norfenfluramine is the major hepatic metabolite of (+)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects; (+)-norfenfluramine causes vasoconstriction and a blood pressure increase in rats with normal blood; acts primarily on the cytoplasmic pool of serotonin; more potent than fenfluramine at inducing dopamine release. |
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