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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.
M14750 o-Toluic acid o-Toluic acid (2-Methylbenzoic acid) is a benzoic acid substituted by a methyl group at position 2. O-Toluic acid plays a role as a xenobiotic metabolite.
M14747 NSC668394 NSC668394 is a potent ezrin (Thr567) phosphorylation inhibitor, with a Kd of 12.59 μM.
M14742 N-Nitrosodibutylamine N-Nitrosodibutylamine (N-Nitroso-di-n-butylamine) is a nitrosamine enriched in the drinking water.
M14737 N-Bis(2-hydroxypropyl)nitrosamine N-Bis(2-hydroxypropyl)nitrosamine is an agent with carcinogenic activity.
M14729 Mexenone Mexenone is a potent benzophenone-type UV filter. Mexenone is used for sunscreening agent.
M14723 Lith-O-Asp Lith-O-Asp is a sialytransferase (ST) inhibitor, with IC50s of 12-37 μM.
M14722 Levobunolol hydrochloride Levobunolol hydrochloride is a non-selective beta blocker. It is used topically to manage glaucoma.
M14721 KRN2 bromide KRN2 (bromide) is a selective inhibitor of nuclear factor of activated T cells (NFAT5), with an IC50 of 0.1 μM.
M14717 Iodipamide Iodipamide is a tri-iodinated benzoate derivative and ionic dimeric contrast agent used in diagnostic imaging.
M14714 HC-056456 HC-056456 is an effective but not perfectly-selective blocker of CatSper channels. The [Na+]i rise is slowed by HC-056456 (IC50~3 µM).
M14712 GSK 525768A GSK 525768A is the inactive enantiomer of GSK525762A. GSK 525768A has no activity towards BET.
M14711 Glyoxalase I inhibitor free base Glyoxalase I inhibitor (free base) is a potent Glyoxalase I (GLO1) inhibitor, candidate for anticancer agents.
M14710 Glyoxalase I inhibitor Glyoxalase I inhibitor is a potent Glyoxalase I inhibitor, candidate for anticancer agents.
M14709 Glycerophosphoric acid disodium salt hydrate (α and β mixture) Glycerophosphoric acid (disodium salt hydrate) (α and β mixture) is a complex contains α and β Glycerophosphoric acid isomers.
M14708 GKI-1 GKI-1 is a Greatwall (GWL) kinase inhibitor with IC50s of 4.9 and 2.5 µM against hGWLFL and hGWL-KinDom, respectively. GKI-1 robustly inhibits ROCK1 with an IC50 of 11 µM, but only weakly affected PKA.
M14705 Gadodiamide Gadodiamide(Omniscan) is a gadolinium-based MRI contrast agent, used in MR imaging procedures to assist in the visualization of blood vessels.
M14702 Fluorene Fluorene, a polycyclic aromatic hydrocarbon (PAH), is a precursor to other fluorene compounds. Fluorene and its derivative can be used as a precursor to fluorene-based dyes.
M14699 Ethyl docosa-4,7,10,13,16,19-hexaenoate Ethyl cis-4,7,10,13,16,19-Docosahexaenoate, the ethyl ester of Docosahexaenoate (DHA), is enriched in the ethyl ester fraction by the selective alcoholysis of fatty acid ethyl esters originating from tuna oil with lauryl alcohol.
M14695 E-982 E-982 is a steroid used for the on-line screening of the DNA unwinding element binding protein (DUE-B) immobilized protein column.
M14693 DZ2002 DZ2002 is a potent and reversible S-Adenosyl-L-homocysteine Hydrolase(SAHH; AdoHcy Hydrolase) inhibitor with Ki of 17.9 nM.




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