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Amyloid β

Amyloid β denotes peptides of 36–43 amino acids result from the APP (amyloid precursor protein) and are involved in Alzheimer's disease as the main component of the amyloid plaques.

  1. Cat.No. Product Name Information
  2. GC63273 β-Amyloid (1-14),mouse,rat β-Amyloid (1-14),mouse,rat  Chemical Structure
  3. GC66089 β-Amyloid (1-40) (TFA) β-Amyloid (1-40) TFA is a primary protein in plaques found in the brains of patients with Alzheimer's disease. β-Amyloid (1-40) (TFA)  Chemical Structure
  4. GC70182 β-Amyloid (1-40), FAM-labeled TFA β-Amyloid (1-40), FAM-labeled TFA  Chemical Structure
  5. GC63274 β-Amyloid (1-42), (rat/mouse) (TFA) β-Amyloid (1-42), (rat/mouse) (TFA)  Chemical Structure
  6. GC37984 β-Amyloid (1-42), rat β-Amyloid (1-42), rat is a 42-aa peptide, shows cytotoxic effect on acute hippocampal slices, and used in the research of Alzheimer's disease. β-Amyloid (1-42), rat  Chemical Structure
  7. GC66416 β-Amyloid (22-35) (TFA) β-Amyloid 22-35 (Amyloid β-Protein 22-35) TFA, the residues 22-35 fragment ofβ-amyloid protein, has a cytotoxic effect on cultured neurons from the rat hippocampus in serum-free medium. β-Amyloid 22-35 TFA forms aggregates and typical amyloid fibrils resembling those of the β-amyloid protein in neutral buffer solution). β-Amyloid (22-35) (TFA)  Chemical Structure
  8. GC66346 β-Amyloid (42-1), human TFA β-Amyloid (42-1), human TFA is the inactive form of Amyloid β Peptide (1-42). β-Amyloid (42-1), human TFA is a 42-amino acid peptide which plays a key role in the pathogenesis of Alzheimer disease. β-Amyloid (42-1), human TFA  Chemical Structure
  9. GC37986 β-Amyloid 1-17 β-Amyloid 1-17 is a peptide of β-Amyloid, stabilizes the fibres and plays a role in Aβ fibre formation. β-Amyloid 1-17  Chemical Structure
  10. GC37987 β-Amyloid 1-20 β-Amyloid 1-20 consists of amino acids 1 to 20 of beta amyloid protein. β-Amyloid 1-20  Chemical Structure
  11. GC37993 β-Amyloid 1-9 β-Amyloid 1-9, an N-terminal fragment of beta amyloid, consists of amino acid residues 1 to 9. β-Amyloid 1-9  Chemical Structure
  12. GC37985 β-Amyloid 11-22 β-Amyloid 11-22 is a peptide fragment of β-Amyloid. β-Amyloid 11-22  Chemical Structure
  13. GC37988 β-Amyloid 12-20 β-Amyloid 12-20 is a peptide fragment of β-Amyloid. β-Amyloid 12-20  Chemical Structure
  14. GC37991 β-Amyloid 15-21 β-Amyloid 15-21  Chemical Structure
  15. GC37992 β-Amyloid 18-28 β-Amyloid 18-28 is a peptide fragment of β-Amyloid. β-Amyloid 18-28  Chemical Structure
  16. GC37994 β-Amyloid 22-40 β-Amyloid 22-40 is a peptide fragment of β-Amyloid. β-Amyloid 22-40  Chemical Structure
  17. GC37995 β-Amyloid 33-40 β-Amyloid 33-40 is a peptide consisting of amino acid of 33 to 40 of beta amyloid protein. β-Amyloid 33-40  Chemical Structure
  18. GC37996 β-Amyloid 35-42 β-Amyloid 35-42 is a peptide consisting of amino acid of 35 to 42 of beta amyloid protein. β-Amyloid 35-42  Chemical Structure
  19. GC37997 β-Amyloid 4-10 β-Amyloid 4-10 is an epitope for the polyclonal anti-Aβ(1-42) antibody, reduces amyloid deposition in a transgenic Alzheimer disease mouse model. β-Amyloid 4-10  Chemical Structure
  20. GC34242 β-Amyloid (1-42), rat TFA β-Amyloid (1-42), rat TFA  Chemical Structure
  21. GC31146 β-Amyloid (10-35), amide β-Amyloid (10-35), amide is composed of 26 aa (10-35 residues of the Aβ peptide) and is the primary component of the amyloid plaques of Alzheimer's disease. β-Amyloid (10-35), amide  Chemical Structure
  22. GC31129 β-Amyloid 1-16 (Amyloid β-Protein (1-16)) β-Amyloid 1-16 (Amyloid β-Protein (1-16)) is a β-Amyloid protein fragment involved in metal binding. β-Amyloid 1-16 (Amyloid β-Protein (1-16))  Chemical Structure
  23. GC31171 β-Amyloid 1-28 (Amyloid β-Protein (1-28)) β-Amyloid 1-28 (Amyloid β-Protein (1-28)) is a β-Amyloid protein fragment involved in metal binding. β-Amyloid 1-28 (Amyloid β-Protein (1-28))  Chemical Structure
  24. GC30325 β-Amyloid 22-35 (Amyloid β-Protein (22-35)) β-Amyloid 22-35 (Amyloid β-Protein 22-35), the residues 22-35 fragment ofβ-amyloid protein, has a cytotoxic effect on cultured neurons from the rat hippocampus in serum-free medium. β-Amyloid 22-35 (Amyloid β-Protein (22-35))  Chemical Structure
  25. GC31137 β-Amyloid 29-40 (Amyloid beta-protein(29-40)) β-Amyloid 29-40 (Amyloid beta-protein(29-40)) is a fragment of Amyloid-β peptide. β-Amyloid 29-40 (Amyloid beta-protein(29-40))  Chemical Structure
  26. GC31179 β-Amyloid 31-35 β-Amyloid 31-35 is the shortest sequence of native Amyloid-β peptide that retains neurotoxic activity. β-Amyloid 31-35  Chemical Structure
  27. GC16032 (R,S)-Anatabine Aβ inhibitor (R,S)-Anatabine  Chemical Structure
  28. GC16139 (R,S)-Anatabine (tartrate) Aβ inhibitor (R,S)-Anatabine (tartrate)  Chemical Structure
  29. GC30952 4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine 4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine is a potent amyloid imaging agent which binds to Amyloid-β (1-40) with a KD of 1.7 nM. 4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine  Chemical Structure
  30. GC31208 4-(6-Bromo-2-benzothiazolyl)benzenamine 4-(6-Bromo-2-benzothiazolyl)benzenamine is a β-amyloid PET (positron emission tomography) tracer that can be used in the diagnosis of neurological diseases, such as Alzheimer's and Down's syndrome. 4-(6-Bromo-2-benzothiazolyl)benzenamine  Chemical Structure
  31. GC63502 Aβ/tau aggregation-IN-1 Aβ/tau aggregation-IN-1 is a potent Aβ1-42 β-sheets formation and tau aggregation inhibitor. Aβ/tau aggregation-IN-1  Chemical Structure
  32. GC66406 Aducanumab Aducanumab (BIIB037), a human monoclonal antibody selective for aggregated forms of amyloid beta (Aβ). Aducanumab shows brain penetration, and can be used for Alzheimer's disease (AD) research. Aducanumab  Chemical Structure
  33. GC31259 Aftin-4 An inducer of Aβ42 Aftin-4  Chemical Structure
  34. GC65281 Aleplasinin Aleplasinin is an orally active, potent, BBB-penetrated and selectiveSERPINE1 (PAI-1, Plasminogen activator inhibitor-1) inhibitor. Aleplasinin  Chemical Structure
  35. GC62834 ALZ-801 ALZ-801 is a potent and orally available small-molecule β-amyloid (Aβ) anti-oligomer and aggregation inhibitor, valine-conjugated prodrug of Tramiprosate with substantially improved PK properties and gastrointestinal tolerability compared with the parent compound. ALZ-801  Chemical Structure
  36. GC35334 Amyloid β Peptide (42-1)(human) Amyloid β Peptide (42-1)(human) is the inactive form of Amyloid β Peptide (1-42). Amyloid β Peptide (42-1)(human)  Chemical Structure
  37. GA20733 Amyloid β-Protein (1-42)

    Compared to the inner salt, the HCl salt of Aβ42 aggregates more readily at pH 7.4.

    Amyloid β-Protein (1-42)  Chemical Structure
  38. GA20730 Amyloid β-Protein (1-42) (HFIP-treated) H-7442 was obtained by dissolving Amyloid β-Protein (1-42) (H-1368) in HFIP, aliquoting, and removing the solvent as described in the literature. Amyloid β-Protein (1-42) (HFIP-treated)  Chemical Structure
  39. GA20736 Amyloid β-Protein (1-43) Amyloid β-Protein (1-43) is more prone to aggregation and has higher toxic properties than the long-known Aβ1-42. Amyloid β-Protein (1-43)  Chemical Structure
  40. GP10099 amyloid A protein fragment [Homo sapiens] Apolipoproteins related to HDL in plasma amyloid A protein fragment [Homo sapiens]  Chemical Structure
  41. GP10118 Amyloid Beta-Peptide (1-40) (human) Amyloid Beta-Peptide (1-40) (human)  Chemical Structure
  42. GP10049 Amyloid Beta-Peptide (12-28) (human) Amyloid Beta-Peptide (12-28) (human)  Chemical Structure
  43. GP10082 Amyloid Beta-peptide (25-35) (human) Amyloid Beta-peptide (25-35) (human)  Chemical Structure
  44. GC33160 amyloid P-IN-1 amyloid P-IN-1 is used in the research of diseases or disorders wherein depletion of serum amyloid P component (SAP), including amyloidosis, Alzheimer's disease, type 2 diabetes mellitus and osteoarthritis. amyloid P-IN-1  Chemical Structure
  45. GP10046 Amyloid Precursor C-Terminal Peptide

    For beta amyloid generation

    Amyloid Precursor C-Terminal Peptide  Chemical Structure
  46. GP10057 Amyloid β-Peptide (10-20) (human) Amyloid β-Peptide (10-20) (human)  Chemical Structure
  47. GP10094 Amyloid β-peptide (10-35), amide Amyloid β-peptide (10-35), amide  Chemical Structure
  48. GP10097 Amyloid β-Protein (1-15) Amyloid β-Protein (1-15)  Chemical Structure
  49. GC39254 Anatabine dicitrate Anatabine dicitrate is a tobacco alkaloid that can cross the blood-brain barrier. Anatabine dicitrate  Chemical Structure
  50. GC11309 ARN2966

    APP expression modulator

    ARN2966  Chemical Structure
  51. GC19053 Azeliragon TTP488 is an antagonist at the Receptor for Advanced Glycation End products, is evaluated as a potential treatment for patients with mild-to-moderate Alzheimer's disease (AD). Azeliragon  Chemical Structure
  52. GP10083 Beta-Amyloid (1-11) Beta-Amyloid (1-11)  Chemical Structure
  53. GC34232 Beta-Amyloid(1-14),mouse,rat Beta-Amyloid(1-14),mouse,rat  Chemical Structure
  54. GC31124 BF 227

    BF 227 is a candidate for an amyloid imaging probe for PET, with a Ki of 4.3 nM for Aβ1-42 fibrils.

    BF 227  Chemical Structure
  55. GC33750 BF-168 BF-168, a candidate probe for PET, is found to specifically recognize both neuritic and diffuse plaques, with a Ki of 6.4 nM for Aβ1-42. BF-168  Chemical Structure
  56. GC15950 CGP 52411 EGFR inhibitor CGP 52411  Chemical Structure
  57. GC61887 Cl-NQTrp Cl-NQTrp signifcantly disrupts the preformed fbrillar aggregates of Tau-derived PHF6 (VQIVYK) peptide and full-length tau protein. Cl-NQTrp  Chemical Structure
  58. GC14854 Colivelin Colivelin (CLN) is A brain-permeable neuroprotective peptide. Colivelin  Chemical Structure
  59. GC35720 Colivelin TFA Colivelin TFA is a brain penetrant neuroprotective peptide and a potent activator of STAT3, suppresses neuronal death by activating STAT3?in vitro. Colivelin TFA  Chemical Structure
  60. GC14828 CPHPC CPHPC is a ligand for serum amyloid P component (SAP) and intends to inhibit and dissociate SAP binding to amyloid fibrils and tangles. CPHPC  Chemical Structure
  61. GC10230 CRANAD 2 near-infrared probe that binds to Aβ40 aggregates CRANAD 2  Chemical Structure
  62. GC12942 DAPT (GSI-IX) Inhibitor of γ-secretase DAPT (GSI-IX)  Chemical Structure
  63. GC50733 Davunetide Davunetide is an eight amino acid snippet derived from activity-dependent neuroprotective protein (ADNP), a neurotrophic factor that exists in the mammalian CNS. Davunetide  Chemical Structure
  64. GC13554 Deferoxamine mesylate

    Deferoxamine mesylate is a drug that chelates iron by forming a stable complex that prevents the iron from entering into further chemical reactions, and is used for the treatment of chronic iron overload in patients with transfusion-dependent anemias.

    Deferoxamine mesylate  Chemical Structure
  65. GC13256 Dihydroergocristine mesylate 5-HT receptor antagonist and partial agonist of adrenergic and dopaminergic receptors Dihydroergocristine mesylate  Chemical Structure
  66. GC31083 DWK-1339 (MDR-1339) DWK-1339 (MDR-1339) (DWK-1339) is an orally active and blood-brain-barrier-permeable Aβ-aggregation inhibitor, used in the research of Alzheimer's disease. DWK-1339 (MDR-1339)  Chemical Structure
  67. GC30823 Edonerpic maleate (T-817 maleate) Edonerpic maleate (T-817 maleate) is a novel neurotrophic agent which can inhibit amyloid-β peptides (Aβ). Edonerpic maleate (T-817 maleate)  Chemical Structure
  68. GC10660 EHT 1864 Rac family small GTPases inhibitor EHT 1864  Chemical Structure
  69. GC10089 EUK 134 Salen-manganese complexes;SOD mimetic EUK 134  Chemical Structure
  70. GC62966 Ezeprogind disulfate Ezeprogind disulfate  Chemical Structure
  71. GC61476 Fmoc-Ala-Glu-Asn-Lys-NH2 Fmoc-Ala-Glu-Asn-Lys-NH2 is a selective asparagine endopeptidase (AEP) inhibitor peptide and suppresses amyloid precursor protein (APP) cleavage. Fmoc-Ala-Glu-Asn-Lys-NH2  Chemical Structure
  72. GC15105 FPS-ZM1 A RAGE Inhibitor FPS-ZM1  Chemical Structure
  73. GC36076 Frentizole Frentizole, an FDA-approved immunosuppressant, is a Aβ-ABAD (binding alcohol dehydrogenase) interaction inhibitor with an IC50 value of 200 μM. Frentizole  Chemical Structure
  74. GC36110 gamma-Secretase Modulators gamma-Secretase Modulators (Amyloid-β production inhibitor) is a Amyloid-β production inhibitor. gamma-Secretase Modulators  Chemical Structure
  75. GN10428 Geniposide Geniposide  Chemical Structure
  76. GN10307 Ginsenoside Re Ginsenoside Re  Chemical Structure
  77. GN10544 Ginsenoside Rg1 Ginsenoside Rg1  Chemical Structure
  78. GN10614 Ginsenoside Rg2 Ginsenoside Rg2  Chemical Structure
  79. GN10799 Ginsenoside Rg3 Ginsenoside Rg3  Chemical Structure
  80. GC30892 Glutaminyl Cyclase Inhibitor 1 Glutaminyl Cyclase Inhibitor 1 is a glutaminyl cyclase inhibitor with an IC50 of 0.5 μM. Glutaminyl Cyclase Inhibitor 1  Chemical Structure
  81. GC31110 Glutaminyl Cyclase Inhibitor 2 Glutaminyl Cyclase Inhibitor 2 is a glutaminyl cyclase inhibitor with an IC50 of 1.23 μM. Glutaminyl Cyclase Inhibitor 2  Chemical Structure
  82. GC36156 Glutaminyl Cyclase Inhibitor 3 Glutaminyl Cyclase Inhibitor 3 (compound 212 ), a designed anti-Alzheimer’s compound, is a potent human Glutaminyl Cyclase (GC) inhibitor, with an IC50 of 4.5 nM. Glutaminyl Cyclase Inhibitor 3  Chemical Structure
  83. GC17657 Hoechst 34580

    The nucleic acid stain Hoechst 34580 (Ex/Em: 392/440 nm) is frequently utilized as a cell-permeable nuclear counterstain that emits a blue fluorescence upon binding to dsDNA.

    Hoechst 34580  Chemical Structure
  84. GC36247 Hoechst 34580 tetrahydrochloride

    The nucleic acid stain Hoechst 34580 tetrahydrochloride (Ex/Em: 392/440 nm) is frequently utilized as a cell-permeable nuclear counterstain that emits a blue fluorescence upon binding to dsDNA.

    Hoechst 34580 tetrahydrochloride  Chemical Structure
  85. GC10988 J 147 reduces soluble Aβ40 and Aβ42 levels J 147  Chemical Structure
  86. GC30920 K 01-162 (K162) K 01-162 (K162) (K162) inhibits the fibril formation of Aβ peptides and eliminates their neurotoxicity. K 01-162 (K162)  Chemical Structure
  87. GC17974 Latrepirdine dihydrochloride Latrepirdine is a neuroactive compound with antagonist activity at histaminergic, α-adrenergic, and serotonergic receptors. Latrepirdine dihydrochloride  Chemical Structure
  88. GC38628 Licochalcone B Licochalcone B  Chemical Structure
  89. GC12366 LPYFD-NH2 neuroprotective peptide that binds to amyloid beta (Aβ) LPYFD-NH2  Chemical Structure
  90. GC30884 LX2343 An inhibitor of BACE1 and PI3K LX2343  Chemical Structure
  91. GC10894 Methoxy-X04

    Fluorescent amyloid β (Aβ) probe

    Methoxy-X04  Chemical Structure
  92. GC31285 MK-3328 MK-3328 is a β-Amyloid PET ligand, which exhibits high binding potency with an IC50 of 10.5 nM. MK-3328  Chemical Structure
  93. GN10695 Notoginsenoside R1 Notoginsenoside R1  Chemical Structure
  94. GC17037 NQTrp inhibitor of Alzheimer’s disease-associated amyloid β (Aβ) oligomerization and fibrillization NQTrp  Chemical Structure
  95. GC68377 OAB-14 OAB-14  Chemical Structure
  96. GC13783 Phenserine acetylcholinesterase inhibitor Phenserine  Chemical Structure
  97. GC36954 PQM130 PQM130, a Feruloyl-Donepezil Hybrid compound with brain penatration, is a multitarget drug candidate against the neurotoxicity induced by Aβ1-42 oligomer (AβO) and shows anti-inflammatory activity. PQM130  Chemical Structure
  98. GC62702 RAGE antagonist peptide TFA RAGE antagonist peptide TFA is an advanced glycation end products (RAGE) antagonist. RAGE antagonist peptide TFA  Chemical Structure
  99. GC10425 Ro 90-7501

    Inhibitor of amyloid β42 (Aβ42) fibril assembly

    Ro 90-7501  Chemical Structure
  100. GC44856 Rutin (hydrate) Rutin (Rutoside) trihydrate is a multifunctional natural flavonoid glycoside. Rutin (hydrate)  Chemical Structure
  101. GN10502 Saikosaponin C Saikosaponin C  Chemical Structure

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