Beta Amyloid

Beta Amyloid

As the primary component of the amyloid plaques seen in the brains of Alzheimer patients, amyloid- (A) refers to peptides of 36–43 amino acids that are crucially involved in Alzheimer's disease. The amyloid precursor protein (APP), which is cut by specific enzymes to produce A, produces the peptides. Amyloid molecules can group together to create a variety of flexible, soluble oligomers.A amyloid-peptide buildup results from excessive A production or malfunctioning clearance mechanisms. Amyloid- forms diffuse and neuritic plaques in the parenchyma and blood vessels by self-aggregating into oligomers of various sizes. Strong synaptotoxins, proteasome inhibition, mitochondrial inhibition, alteration of intracellular Ca2+ levels, and induction of inflammatory processes are all characteristics of amyloid-oligomers and plaques. Neuronal dysfunction is also thought to be influenced by the loss of A's typical physiological functions.

Beta Amyloid related products

Structure Cat No. Product Name CAS No. Product Description
V71443 7-Deoxy-trans-dihydronarciclasine 145987-74-2 7-Deoxy-trans-dihydronarciclasine is an alkaloid and an inhibitor (blocker/antagonist) of tobacco mosaic virus (TMV) (IC50= 1.80 μM).
V71439 [Ala28]-β Amyloid(25-35) (β(25-35)KA) 173993-86-7 [Ala28]-β Amyloid(25-35) (β(25-35)KA) is an electroneutral mutant peptide of Aβ(25-35) that accelerates the aggregation of firefly luciferase.
V71378 [Arg6]-β-Amyloid (1-40), england mutation 1802084-26-9 [Arg6]-β-Amyloid (1-40), england mutation is a biologically active peptide.
V77472 [Arg6]-β-Amyloid (1-42), england mutation [Arg6]-β-Amyloid (1-42), england mutation is a biologically active peptide.
V71392 [Asn23] β-Amyloid (1-40), Iowa mutation 374796-72-2 [Asn23] β-Amyloid (1-40), Iowa mutation is a biologically active peptide.
V77473 [Asn23]-beta-Amyloid (1-42), iowa mutation [Asn23]-beta-Amyloid (1-42), iowa mutation is a biologically active peptide.
V71399 AC 253 151804-79-4 AC 253 is an antagonist of amylin, inhibiting 125I-adrenomedullin binding, with IC50 of 25 nM.
V71397 Acetly-β Amyloid(15-20), Amide 189064-06-0 Acetly-β Amyloid (15-20), Amide is a polypeptide fragment.
V71434 Acetyl-Amyloid β-Protein (1-6) amide 903883-22-7 Acetyl-Amyloid β-Protein (1-6) amide is a hexapeptide that contains potential copper(II) binding sites.
V71431 Acetyl-Tau Peptide (273-284)amide 1684399-52-7 Acetyl-Tau Peptide (273-284) amide is an acetylated Tau peptide fragment.
V79836 AChE/Aβ-IN-1 AChE/Aβ-IN-1 (compound 32) is a potent oral acetylcholinesterase (AChE) inhibitor (antagonist) with IC50 of 86 nM and an NMDA receptor (GluN1-1b/GluN2B subunit combination) antagonist.
V79835 AChE/Aβ-IN-2 AChE/Aβ-IN-2 (compound 32) is a potent oral acetylcholinesterase (AChE) inhibitor (antagonist) with IC50 of 86 nM and an NMDA receptor (GluN1-1b/GluN2B subunit combination) antagonist.
V79262 AChE/BChE-IN-12 AChE/BChE-IN-12 (compound 10b), a 3,5-dimethoxy analog, is a potent inhibitor of AChE, BChE and beta-secretase-1 (BACE-1) with IC50s respectively are 2.57, 3.26 and 10.65 μM.
V79102 AChE/MAO-B-IN-3 AChE/MAO-B-IN-3 (Compound D30) is an inhibitor (blocker/antagonist) of AChE and MAO-B, with IC50 of 0.0257 μM and 0.0456 μM for human AChE and MAO-B, respectively.
V79287 AChE/MAO-IN-1 AChE/MAO-IN-1 (Compound D28) is a potent inhibitor of AChE, MAO-A and MAO-B with IC50 of 0.0248, 0.0409 and 0.1108 μM for human AChE, MAO-B and MAO-A respectively.
V29026 Aftin-4 866893-90-5 Aftin-4 is an inducer of beta-amyloid 42 (Aβ42).
V10910 ALZ-801 1034190-08-3 ALZ-801 (ALZ801; BLU-8499; NRM-8499) is an orally bioavailable, small-molecule inhibitor of beta amyloid (Aβ) oligomer formation with the potential for treating Alzheimers disease (AD).
V71385 Amyloid β-Protein (1-12) 142047-91-4 Amyloid β-Protein (1-12) is a bioactive peptide discovered by peptide screening.
V71410 Amyloid β-Protein (1-24) 138648-77-8 Amyloid β-Protein (1-24) is a bioactive peptide discovered by peptide screening.
V71419 Amyloid β-Protein (1-46) 285554-31-6 Amyloid β-Protein (1-46) is an Aβ fragment.
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