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Results for "

amyloid β

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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Cys-Gly-Lys-Lys-Gly-Amyloid β-Protein (36-42)
T763941802078-25-6
Amyloid β-Protein (36-42), the 36-42 fragment of β-Amyloid, consists of a polypeptide chain of 36-43 amino acids and is a primary constituent of amyloid plaques in Alzheimer's disease (AD) patients' brains. β-Amyloid oligomers (Aβos) critically contribute to AD progression by causing neuronal harm and cognitive decline [1].
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(Met(O)35)-Amyloid β-Protein (1-42)
T76395
(Met(O)35)-Amyloid β-Protein (1-42) is the oxidized form of Methionine 35 in Aβ42, capable of producing an oligomer size distribution similar to Aβ40. This compound is utilized in Alzheimer's disease (AD) research [1].
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(Met(O2)35)-Amyloid β-Protein (1-42)
T76396
(Met(O2)35)-Amyloid β-Protein (1-42) is a peptide [1].
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(Nle35)-Amyloid β-Protein (1-42) (ammonium)
T76397
(Nle35)-Amyloid β-Protein (1-42) ammonium is a peptide.
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Amyloid β-Protein (33-42) (TFA)
T76401
Amyloid β-Protein (33-42) TFA, encompassing residues 33-42 of the β-amyloid protein, mitigates the toxicity induced by Aβ42 [1].
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(Gly22)-Amyloid β-Protein (1-42)
T764241802086-23-2
(Gly22)-Amyloid β-Protein (1-42), a peptide fragment of Amyloid β-Protein (Aβ), plays a crucial role in Alzheimer's disease by forming the main component of vascular and parenchymal amyloid deposits. The Glu22 to Gly22 mutation in Aβ is known to enhance aggregation [1] [2].
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(Glu20)-Amyloid β-Protein (1-42)
T764251802086-22-1
(Glu20)-Amyloid β-Protein (1-42) represents a variant of amyloid β-protein (Aβ) that fibrillizes more slowly due to the Glu20 mutation, which diminishes Aβ42's tendency to aggregate and inhibits the accumulation of this slowly fibrillizing peptide. Amyloid β-protein is the principal constituent of amyloid deposits in the vascular system and brain parenchyma in Alzheimer's disease [1] [2].
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(D-Asp1)-Amyloid β-Protein (1-42)
T764321802086-19-6
(D-Asp1)-Amyloid β-Protein (1-42), a peptide fragment of amyloid β-protein (Aβ), serves as the primary constituent of vascular and parenchymal amyloid deposits associated with Alzheimer's disease [1].
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Cys-Gly-Lys-Arg-Amyloid β-Protein (1-42)
T764331802086-21-0
Cys-Gly-Lys-Arg-Amyloid β-Protein (1-42), a peptide fragment derived from amyloid β-protein (Aβ), is crucial in Alzheimer's disease research [1].
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Biotinyl-Amyloid β-Protein (1-42) (ammonium)
T76434
Biotinyl-Amyloid β-Protein (1-42) ammonium, a biotinylated form of Amyloid β-Protein (1-42), is used in research on the conversion of Aβ1-42 to Aβ1-40 in the brain [1].
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FITC-β-Ala-Amyloid β-Protein (1-42) (ammonium)
T76464
FITC-β-Ala-Amyloid β-Protein (1-42) ammonium, a fluorescein isothiocyanate (FITC)-tagged monomer peptide of Aβ1-42, is instrumental in Alzheimer's disease pathogenesis [1].
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Biotinyl-Ahx-Amyloid β-Protein (1-42) (ammonium)
T76465
Biotinyl-Ahx-Amyloid β-Protein (1-42) ammonium is an N-terminally biotin-tagged form of Amyloid β-Protein (1-42), the primary component of vascular and parenchymal amyloid deposits associated with Alzheimer's disease [1].
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(Asp37)-Amyloid β-Protein (1-42)
T765881875128-79-2
'(Asp37)-Amyloid β-Protein (1-42) [1]' refers to the G37D mutant variant of the wild-type Amyloid-beta (1-42) peptide.
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(Gln22)-Amyloid β-Protein (1-42)
T76623147335-12-4
(Gln22)-Amyloid β-Protein (1-42), a Dutch mutation (E22Q) variant of β-Amyloid (1-42), exhibits enhanced fibrillogenic and pathogenic properties [1].
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(Lys22)-Amyloid β-Protein (1-42)
T76625383200-59-7
'(Lys22)-Amyloid β-Protein (1-42) represents a mutation of the wild-type (WT) Amyloid β-Protein (1-42) peptide [1].'
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Acetyl-Amyloid β-Protein (1-6) amide
T76647903883-22-7
Acetyl-Amyloid β-Protein (1-6) amide, a hexapeptide potentially binding copper(II), is used in Alzheimer's disease research and related disorders [1].
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Amyloid β-Protein (3-42)
T83123157884-74-7
Amyloid β-Protein (3-42), the precursor of Pyr peptide, serves as the foundation of the amyloid template block in Alzheimer's disease when modified to pyroglutamate Aβ (pEAβ) (3-42). This modified form, pEAβ(3-42), hastens the aggregation of Aβ(1-42) although Aβ(1-42) markedly decelerates both the primary and secondary nucleation of pEAβ(3-42) [1].
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(Pyr11)-Amyloid β-Protein (11-40)
T83539192377-94-9
(Pyr11)-Amyloid β-Protein (11-40) (Aβ11pE-40), a peptide, is utilized in Alzheimer's disease research [1].
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(Gln22,Asn23)-Amyloid β-Protein (1-40)
T83541374796-75-5
(Gln22,Asn23)-Amyloid β-Protein (1-40) is a peptide used to study Cerebral Amyloid Angiopathy Mutations [1].
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Amyloid β Peptide (42-1)(human) acetate
Amyloid β Peptide (42-1)(human) acetate(317366-82-8 free base)
TP1359L
Amyloid β Peptide (42-1)(human) acetate is the inactive form of Amyloid β Peptide (1-42). Amyloid β Peptide (42-1)(human) acetate is a 42-amino acid peptide which plays a key role in the pathogenesis of Alzheimer disease.
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Amyloid β-Protein 10-20 acetate
Amyloid β-Protein 10-20 acetate(152286-31-2 free base)
TP1786L
Amyloid β-Protein 10-20 acetate (Amyloid β-Protein 10-20 acetate (152286-31-2 free base)) is a fragment of Amyloid-β peptide, maybe used in the research of neurological disease.Amyloid β protein fragment containing the α-secretase processing site (Lys16-Leu17 bond). It also contains the HHQK domain (residues 13-16) responsible for binding to microglial cells.
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Biotin-β-Amyloid (1-42), human TFA
Biotin-amyloid β-peptide (1-42) (human) TFA
T80035
Biotin-β-Amyloid (1-42), human TFA, also known as Biotin-Amyloid β-Peptide (1-42) (human) TFA, is a biotin-labeled 42-amino acid peptide implicated in the pathogenesis of Alzheimer's disease.
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β-Amyloid (1-42), human
β-Amyloid (1-42), human, Amyloid β-Peptide (1-42) human
TP1007107761-42-2
β-Amyloid (1-42), human, is a 42-amino acid peptide integral to the pathogenesis of Alzheimer disease.
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β-Amyloid (31-35)
β-Amyloid 31-35
T7562149385-65-9
β-Amyloid (31-35) (β-Amyloid 31-35) is the shortest sequence of native Amyloid-β peptide.
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