Amyloid-β
货号 | 产品名 | CAS号 | 信息 |
---|---|---|---|
FB08354 | Tramiprosate | 3687-18-1 | Tramiprosate targets soluble Aβ to decrease amyloid plaque deposition and maintains Aβ in a non-fibrillar form. |
FB06996 | PE859 | 1402727-29-0 | PE859 is a Curcumin-derived inhibitor of Amyloid-β and Tau aggregation and can ameliorate cognitive dysfunction in senescence-accelerated mouse Prone 8. |
FB11705 | MK-3328 | 1201323-97-8 | MK-3328 is a β-Amyloid PET ligand, which exhibits high binding potency with an IC50 of 10.5 nM. |
FB00593 | MK-0752 | 471905-41-6 | MK-0752 is a moderately potent γ-secretase inhibitor, which reduces Aβ40 production with IC50 of 5 nM. |
FB06242 | K 01-162 | 677746-25-7 | K 01-162 binds and destabilizes AβO (β-amyloid), with an EC50 of 80 nM. |
FB12987 | HP-β-CD | 128446-35-5 | HP-β-CD is used to improve the solubility of lipophilic drugs. It is also an inhibitor of amyloid-β aggregation and Aβ-induced toxicity. |
FB03927 | Ginsenoside Re | 52286-59-6 | Ginsenoside Re is a panaxatriol saponin that has diverse in vitro and in vivo effects, including vasorelaxant, antioxidant, antihyperlipidemic, and angiogenic actions. |
FB02013 | Frentizole | 26130-02-9 | Frentizole, an immunosuppressive drug, is an inhibitor of the Aβ-ABAD interaction. |
FB01399 | FPS-ZM1 | 945714-67-0 | FPS-ZM1 is a high-affinity RAGE-specific inhibitor that blocks Aβ binding to the V domain of RAGE with Ki of 25 ± 5 nM in RAGE-transfected CHO cells. |
FB09146 | EUK 134 | 81065-76-1 | EUK 134, a synthetic superoxide dismutase (SOD)/catalase mimetic, exhibits potent antioxidant activities, and inhibits the formation of β-amyloid and related amyloid fibril. |
FB12509 | Edonerpic Maleate | 519187-97-4 | Edonerpic maleate can inhibit amyloid-β peptides (Aβ) and used as a neurotrophic agent. |
FB00710 | DWK-1339 | 1018946-38-7 | DWK-1339 is an orally active and blood-brain-barrier-permeable Aβ-aggregation inhibitor, used in the research of Alzheimer's disease. |
FB12690 | CRANAD 2 | 1193447-34-5 | CRANAD-2 is a difluoroboron-derivatized curcumins as near-infrared probe for in vivo detection of amyloid-beta deposits. Upon interacting with Abeta aggregates, CRANAD-2 undergoes a range of changes, which include a 70-fold fluorescence intensity increase, a 90 nm blue shift (from 805 to 715 nm), and a large increase in quantum yield. Moreover, this probe also shows a high affinity for Abeta aggregates (K(d) = 38.0 nM), a reasonable log P value (log P = 3), considerable stability in serum, and a weak interaction with albumin. After intravenous injection of this probe, 19-month-old Tg2576 mice exhibited significantly higher relative signal than that of the control mice over the same period of time. |
FB17598 | Colivelin TFA | N/A | Colivelin TFA is a brain penetrant neuroprotective peptide and a potent activator of STAT3, suppresses neuronal death by activating STAT3 in vitro . Colivelin TFA exhibits long-term beneficial effects against neurotoxicity, Aβ deposition, neuronal apoptosis, and synaptic plasticity deficits in neurodegenerative disease . Colivelin TFA has the potential for the treatment of alzheimer's disease and ischemic brain injury . |
FB01932 | ARN2966 | 102212-26-0 | ARN2966 is a potent post-transcriptional modulator of APP expression and reduces expression of APP with resultant lower production of Aβ. |
FB10116 | Amyloid P-IN-1 | 1819986-22-5 | Amyloid P-IN-1 is a potential compound for treating amyloidosis, Alzheimer's disease, type 2 diabetes mellitus and osteoarthritis. |
FB11565 | Aftin-4 | 866893-90-5 | Aftin-4 is a potent and selective Aβ42 inducer with an EC50 of 30 μM. |
FB11585 | 4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine | 566169-98-0 | 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. |
FB01240 | 2-D08 | 144707-18-6 | 2-D08 interacts with amyloid β, showing an anti-aggregatory and neuroprotective effect. |