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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
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.
M1634 Chitin (practical grade) Chitin is a large, structural polysaccharide found in the cell walls of fungi, the exoskeletons of insects, and certain hard structures in fish and invertebrates.
M1584 6-β-Naltrexol HCl 6-β-Naltrexol has been reported to act as a neutral antagonist with peripheral selectivity in opioid-naïve and opioid-dependent systems in vitro and in vivo.
M1576 Zolpidic Acid Zolpidic Acid
M1572 DiZPK DiZPK is a genetically encoded, highly efficient photocrosslinking amino acid valuable in unveiling the physiological interaction partners of given proteins and their functions.
M1561 Sofosbuvir metabolites GS566500 Sofosbuvir metabolites GS566500
M1500 Sarcosine Sarcosine is a glycine transporter type 1 (GlyT) inhibitor and an N-methyl-D-aspartate (NMDA) receptor co-agonist at the glycine binding site.
M1498 Methylmalonic acid Methylmalonic acid can be used as a substrate in esterification reactions by various catalysts.
M1491 Silver diethyldithiocarbamate Silver diethyldithiocarbamate is used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues.
M1484 N-Phenylacrylamide N-Phenylacrylamide
M1231 Poly-L-lysine (MW 150000~300000) Poly-L-lysine
M58652 SB-T-1214 SB-T-1214 is a new-generation taxoid. SB-T-1214 possesses significant activity against colon cancer spheroids induced by and enriched with drug resistant tumorigenic CD133high/CD44high cells and efficiently inhibited expression of the majority of stem cell-related genes.
M58649 NG-497 NG-497 is a selective human adipose triglyceride lipase (ATGL) inhibitor that targets the enzymatically active patatin-like domain of human ATGL.




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