| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M2483 | Cabazitaxel | Cabazitaxel (XRP6258) is a semi-synthetic derivative of a natural taxoid. |
| M2458 | Bismuth Subsalicylate | Bismuth Subsalicylate is the active ingredient in Pepto-Bismol and inhibits prostaglandin G/H Synthase 1/2. |
| M2457 | Bisacodyl | Bisacodyl is a stimulant laxative agent. Bisacodyl increases the secretion of PGE2 by direct activation of colon macrophages. |
| M2414 | Azaguanine-8 | Azaguanine-8 is a purine analogs showing antineoplastic activity by competing with guanine in the metabolism. |
| M2396 | Anisindione | Anisindione is a synthetic anticoagulant and an indanedione derivative. |
| M2389 | Amoxapine | Amoxapine is a tricyclic dibenzoxazepine (an N-aryl piperazine) which acts similarly to several other tricyclic antidepressants, amoxapine inhibits GLYT2a transport activity with IC50 of 92 μM. Amoxapine is also a potent GUSB (β-glucuronidase) inhibitor. |
| M2386 | Amikacin disulfate | Amikacin sulfate binds to 16S rRNA (bacterial 30S ribosome), causing misreading of mRNA and supressing proteins synthesis. |
| M2382 | Amfenac Sodium Monohydrate | Amfenac Sodium monohydrate is a non-steroidal analgesic anti-inflammatory compound with acetic acid moiety. |
| M2373 | Allylthiourea | Allylthiourea is a metabolic inhibitor that selective inhibits ammonia oxidation. |
| M2369 | AdipoRon | AdipoRon is a novel, and orally bioavailable adiponectin receptor agonist with KD of 1.8 and 3.1 μM for AdipoR1 and AdipoR2, respectively. |
| M2367 | Acesulfame K | Acesulfame potassium is a non-nutritive sweetener. |
| M2355 | 1-Hexadecanol | 1-Hexadecanol is a fatty alcohol used to make other chemicals. 1-hexadecanol acts as a ferroptosis activator. |
| M2351 | (Z)-Pugnac | (Z)-Pugnac is a potent O-GlcNAc-β-N-acetylglucosaminidase (O-GlcNAcase, OGA) and β-hexosaminidase inhibitor with Ki of 46 nM and 36 nM respectively. |
| M2281 | Exemestane | Exemestane, a kind of Aromatase (CYP19A1) inhibitor, more profoundly inhibited the cell proliferation of KKU-213 cells highly expressing CYP19A1, and inhibited Aromatase in human placenta and rat ovary, with IC50 of 30 nM and 40 nM, respectively. |
| M2273 | Clodronate disodium | Clodronate disodium is the disodium salt of a nitrogen-free bisphosphonate analog of naturally occurring pyrophosphate. |
| M2246 | Bumetanide | Bumetanide is a loop diuretic that inhibits the NKCC cotransporter. |
| M2208 | Lomitapide | Lomitapide (AEGR-733, BMS-201038) is an inhibitor of microsomal triglyceride-transfer protein (MTP) wtih in vitro IC50 of 8 nM. |
| M2107 | Calcium levofolinate | Calcium levofolinate is a calcium salt of folinic acid that is an adjuvant used in cancer chemotherapy. |
| M2085 | Tie2 kinase inhibitor | Tie2 kinase inhibitor is a potent, reversible, and ATP-binding site-targeting Tie2 inhibitor with an IC50 of 250 nM. |
| M1868 | NXY-059 | NXY-059 is a free radical-trapping neuroprotectant that has been reported to reduce infarct size and preserve brain function in experimental models of acute ischemic stroke. |
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