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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.
M7887 α-Linolenic acid An ω-3 fatty acid that serves as a precursor to eicosapentaenoic acid (EPA) but not docosahexaenoic acid.
M7884 Lidocaine N-ethyl chloride Lidocaine N-ethyl chloride is an intracellular voltage-gated sodium channel blocker.
M7873 Kynurenic acid Kynurenic acid is a non-selective antagonist at NMDA and AMPA/kainate receptors; blocks kainic acid neurotoxicity.
M7867 JNJ-10198409 JNJ-10198409 is a potent ATP-competitive inhibitor of Platelet-Derived Growth Factor receptor tyrosine kinase (PDGF-RTK) with both antiangiogenic and a direct tumor cell antiproliferative activity.
M7858 Ibandronate sodium salt Ibandronate sodium inhibits farnesyl diphosphate synthase (IC50 = 20 nM).
M7851 ITX3 ITX3 is a specific inhibitor of endogenous TrioN activity acting on the GEF domain and selective cell active inhibitor of the Trio/RhoG/Rac1 pathway.
M7820 GW8510 GW8510 is an inhibitor of cyclin kinase 2 (CDK2).
M7804 5-Fluoro-2′-deoxycytidine 5-Fluoro-2′-deoxycytidine is a mechanism based DNMT (DNA cytosine-5 methyltransferase) inhibitor, that forms a covalent link with the cysteine residue in the active site of DNMT.
M7802 Fadrozole hydrochloride Fadrozole is a nonsteroidal aromatase inhibitor.
M7773 dPPA Selective activator of PKC beta.
M7761 Diacylglycerol Kinase Inhibitor II Diacylglycerol kinase inhibitor.
M7746 Dexrazoxane Dexrazoxane (ICRF-187, ADR-529, DXZ) is an iron chelator that can be used to prevent DOX-induced cardiotoxicity.
M7741 DNQX DNQX is a competitive kainate, quisqualate (non-NMDA) glutamate receptor antagonist.
M7720 Caerulomycin A Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties.
M7696 Choline bitartrate Choline bitartrate is a precursor of the neurotransmitter acetylcholine and acts as a methyl donor in various metabolic processes and lipid metabolism.
M7643 Bongkrekic acid solution An antiapoptotic agent, it protects against NMDA receptor induced neuronal apoptosis,­ extends cell survival in cells undergoing apoptosis following infection with viral vectors and abrogates apoptosis induced by hydrogen peroxide in T-cells.
M7639 BF-170 hydrochloride BF-170 is a new probe for neurofibrillary tangles (tau fibrils).
M7621 Auraptene Auraptene is an estrogen receptor modulator that also acts as an ACAT inhibitor.
M7610 Ancitabine hydrochloride Antineoplastic.
M7602 Acepromazine maleate Acepromazine is a phenothiazine antipsychotic compound commonly used as a veterinary drug (horse, dog, and cat).




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