| 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 |
| M8375 | S 26948 | S 26948 is a selective PPARγ modulator (SPPARγM). |
| M8374 | JK-P3 | JK-P3 is a VEGFR-2 inhibitor. |
| M8373 | NPC26 | NPC26 induces mitochondrial fragmentation and cell death in RAS expressing cells, similar to erastin. |
| M8370 | NCTT-956 | NCTT-956 is a very potent, specific inhibitor of 12-lipoxygenase (12-LO) activity, with an IC50 of 800 nM, no activity against 5-LO and greater than 25-fold selectivity over 15-LO. |
| M8368 | BQCA | BQCA is a potent muscarinic M1 receptor positive allosteric modulator with selectivity for M1 over M2-M5. |
| M8366 | DDN | DDN (5,8-Diacetyloxy-2,3-dich |
| M8365 | BI-87G3 | BI-87G3 is a cell-permeable, potent and selective competitive inhibitor of the c-Jun N-terminal kinase (JNK). |
| M8364 | Azamulin | Azamulin is a derivative of the antibiotic pleuromutilin. |
| M8363 | DpC | DpC is an iron-chelating agent. |
| M8362 | 3CAI | 3CAI is an orally active, potent and specific allosteric inhibitor of Akt1 and Akt2 that directly binds to Ak1 and Akt2 in an ATP noncompetitive manner. |
| M8361 | Qc1 | Qc1 is a reversible inhibitor of threonine dehydroxygenase (TDH). |
| M8360 | CGP36742 | CGP36742 was the first orally active GABAB-selective antagonist. |
| M8356 | ES936 | ES936 is a very potent and selective inhibitor of NAD(P)H:quinone oxidoreductase 1 (NQO1). |
| M8353 | SPA0355 | SPA0355 inhibits cytokine and LPS-induced activation of NF-kB in cell-based assays, blocking IKK-2 phosphorylation, degradation, and p65 binding to DNA. |
| M8352 | BPD | BPD inhibits LPS-induced NF-kB signaling by inactivation of TAK-1. |
| M8350 | Methylhexanamine hydrochloride | Methylhexanamine is a naturally substance isolated from Pelargonium graveolen. |
| M8349 | AE9C90CB | AE9C90CB is a muscarinic acetylcholine receptor antagonist with 20-fold selectivity for M3 receptor subtypes compared to M2. |
| M8347 | SM-7368 | SM-7368 is a cell-permeable inhibitor of TNF-α-induced MMP-9 upregulation. |
| M8346 | AZ513 | AZ513 is a reversible, noncompetitive FAAH inhibitor. |
| M8343 | BNS-22 | BNS-22 is a derivative of natural product GUT-70 isolated from the stem bark of Calophyllum brasiliense exhibits antiproliferative activity against human cancer cells. |
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