| 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 |
| M8398 | 21H7 | 21H7 is an inhibitor of Wnt/β-catenin signaling that act downstream of the symb-catenin destruction complex to inhibit both Wnt-induced and cancer associated constitutive Wnt signaling via destabilization of β-catenin. |
| M8396 | VU0359595 | VU0359595 is a PLD1 specific inhibitor with an IC50 of 3. |
| M8395 | REDD1 inducer | 6-(1,3-Dioxo-6-(piperidin |
| M8393 | NN414 | NN414 is a potent Kir6. |
| M8389 | SR 27417 | SR 27417 is a long-acting, highly potent, specific competitive platelet-activating factor (PAF) receptor antagonist. |
| M8387 | MI-1 | MI-1 is a Menin-MLL interaction inhibitor. |
| M8386 | IWP-3 | IWP-3 is a Wnt inhibitor that prevents palmitylation of Wnt proteins by Porcupine (Porcn). |
| M8384 | Clonixin | Clonomycin is a non - steroidal anti - inflammatory compound (NSAID) with analgesic effect. |
| M8383 | BIM5078 | BIM5078 is a potent Hepatocyte nuclear factor 4a (HNF4a) antagonist that directly binds to ligand-binding pocket and modulates the expression of known HNF4a target genes. |
| M8381 | JM6 | JM6 is a precursor compound inhibitor of Kynurenine 3-monooxygenase (KMO) that increases kynurenine acid levels and reduces extracellular glutamate in the brain. |
| M8378 | DCAP | DCAP is a potent broad-spectrum antibiotic that specifically targets the membranes of both Gram-positive and Gram-negative bacteria. |
| M8377 | UCM710 | UCM710 is a dual inhibitor of fatty acid amide hydrolase (FAAH) and α/β hydrolase domain 6 (ABHD6) the enzymes that hydrolyze endocannabinoids. |
| M8376 | BLT-4 | BLT-4 is a blocker of lipid transport-4 (BLT-1). |
| 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). |
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