| 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 |
| M57025 | ARN19702 | ARN19702 is a selective, orally active, reversible, and brain-penetrant N-acylethanolamine acid amidase (NAAA) inhibitor with an IC50 of 230 nM for human NAAA. |
| M57024 | Axomadol | Axomadol (EN3324) is a centrally active analgesic agent with opioid agonistic properties and inhibitory effects on the reuptake of monoamines. |
| M57023 | TDRL-551 | TDRL-551 is a potent replication protein A (RPA) inhibitor (IC50=18 µM). |
| M57022 | FR901463 | FR901463 is a potent anti-cancer agent and can be used for cancer research. |
| M57021 | FR901465 | FR901465 is a potent anti-cancer and anti-tumor agent. |
| M57020 | Euquinine | Euquinine is an odorless salt that can be used as a substitute for quinine. |
| M57019 | Clomazone | Clomazone is a broad spectrum herbicide used for control of annual grasses and broadleaf weeds in cotton, peas, pumpkins, soybeans, sweet potatoes, and tobacco. |
| M57018 | TC HSD 21 | TC HSD 21 is a potent 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) inhibitor with an IC50 of 14 nM. |
| M57016 | QDPR-IN-1 | QDPR-IN-1 is a potent QDPR inhibitor with an IC50 of 0.72 μM. |
| M57015 | MZ-101 | MZ-101 is a glycogen synthase 1 (GYS1) inhibitor. |
| M57014 | BDP-13176 | BDP-13176 is a potent fascin 1 inhibitor, with a Kd of 90 nM and an IC50 of 240 nM. |
| M57013 | MDH1-IN-2 | MDH1-IN-2 is a potent and selelctive inhibitor of MDH1 with an IC50 of 2.27 μM. |
| M57012 | MDH1-IN-1 | MDH1-IN-1 is a potent inhibitor of MDH1 with an IC50 of 6.79 μM. |
| M57011 | Ethiazide | Ethiazide is a thiazole diuretic which inhibits renal reabsorption of sodium and water, thereby increasing urine excretion, reducing fluid retention, and lowering blood volume and blood pressure. |
| M57010 | GV-150013 | GV-150013 is a selective CCK-B receptor antagonist. |
| M57009 | AR-C67085 | AR-C67085 (PSB 0413; FPL 67085) is a potent platelet P2T receptor antagonist with an pIC50 value of 8.60. |
| M57008 | AS1134900 | AS1134900 is a highly selective, allosteric and uncompetitive NADP+-dependent malic enzyme 1 (ME1) inhibitor. |
| M57007 | TNIK-IN-7 | TNIK-IN-7 is an inhibitor of Traf2 and Nck-interacting kinase (TNIK), with IC50 of 11 nM, that has antitumor activity. |
| M57006 | NBD-amine | NBD-amine is a fluorogenic amine. |
| M57005 | CBM-301940 | CBM-301940 is an orally active malonate CoA decarboxylase (MCD) inhibitor with IC50 value of 23 nM. |
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