| 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 |
| M7890 | L-365260 | L-365260 is a CCK2 selective antagonist. |
| M7889 | LPK-26 | LPK-26 is an analog of ICI-199441 and (-)U50,488H (classic kappa agonists). |
| M7888 | Levocabastine hydrochloride | Non-peptide histamine H1 receptor antagonist; neurotensin NTS2 receptor ligand. |
| M7884 | Lidocaine N-ethyl chloride | Lidocaine N-ethyl chloride is an intracellular voltage-gated sodium channel blocker. |
| M7883 | L-741,626 | Selective D2 dopamine receptor antagonist. |
| M7882 | Levallorphan tartrate salt | Partial agonist (antagonist) at μ and δ opioid receptors. |
| M7881 | LY-487379 hydrochloride | LY-487379 is a positive allosteric modulator of the metabotropic glutamate receptor mGluR2. |
| M7875 | KRM-III | KRM-III is an inhibitor of T cell antigen receptor (TCR), an inhibitor of phorbol myristate acetate (PMA) /ionomycin-induced nuclear factor of activated T cells (NFAT) activation and T cell proliferation. |
| M7868 | JFD00244 | JFD00244 is a SIRT (sirtuin, human silent information regulator) inhibitor. |
| M7864 | JS-K | Nitric oxide donor; antiproliferative. |
| M7862 | IMS2186 | IMS2186 is an anti-proliferative and anti-angiogenic compound. |
| M7861 | H-7 | Inhibitor of cyclic nucleotide dependent protein kinase (PKA) and protein kinase C. |
| M7860 | ISCK03 | ISCK03 inhibits in vitro phosphorylation of c-Kit in a dose dependent manner. |
| M7859 | Idazoxan hydrochloride | α2-adrenoceptor antagonist; I2 imidazoline receptor agonist; I1 imidazoline receptor antagonist. |
| M7858 | Ibandronate sodium salt | Ibandronate sodium inhibits farnesyl diphosphate synthase (IC50 = 20 nM). |
| M7856 | Immepip dihydrobromide | Immepip is a H3 and H4 histamine receptor agonist. |
| M7855 | ICI 192605 | ICI 192605 is a potent thromboxane A2 receptor antagonist. |
| M7854 | Ilmofosine | Protein Kinase C (PKC) inhibitor; an ether lipid derivative of lysophosphatidylcholine has antineoplastic activity in vitro and in vivo. |
| M7852 | I-AB-MECA | Reference standard for radioiodinated I-AB-MECA, a widely used, high affinity radioligand for the A3 adenosine receptor. |
| M7851 | ITX3 | ITX3 is a specific inhibitor of endogenous TrioN activity acting on the GEF domain and selective cell active inhibitor of the Trio/RhoG/Rac1 pathway. |
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