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Thioflavin T. Group: Biochemicals. Alternative Names: Basic Yellow 1; CI 495. Grades: Highly Purified. CAS No. 2390-54-7. Pack Sizes: 50g, 100g. US Biological Life Sciences.
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Thioflavin T
Thioflavin T is a cationic Benzothiazole dye that shows enhanced fluorescence upon binding to amyloid in tissue sections. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Basic Yellow 1. CAS No. 2390-54-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-D0218.
Thioflavin T ≥90%
Thioflavin T ≥90%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g. US Biological Life Sciences.
2-(4-(dimethylamino)phenyl)-6-methyl-benzothiazole is an uncharged derivative of Thioflavin-T. Group: Biochemicals. Grades: Highly Purified. CAS No. 10205-62-6. Pack Sizes: 25mg, 50mg. Molecular Formula: C16H16N2S, Molecular Weight: 268.38. US Biological Life Sciences.
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2-Phenyl-3,4-dihydro-2H-thiochromene
2-Phenyl-3,4-dihydro-2H-thiochromene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: THIOFLAVIN, CID22251, 5961-99-9. Product Category: Heterocyclic Organic Compound. CAS No. 5961-99-9. Molecular formula: C15H14S. Mole weight: 226.337 g/mol. Purity: 0.96. IUPACName: 2-phenyl-3,4-dihydro-2H-thiochromene. Canonical SMILES: C1CC2=CC=CC=C2SC1C3=CC=CC=C3. Density: 1.132g/cm³. Product ID: ACM5961999. Alfa Chemistry ISO 9001:2015 Certified.
Frentizole
Frentizole is a novel inhibitor of the Aβ-ABAD interaction (IC50 = 200 lM). Frentizole, a nontoxic antiviral and immunosuppressive agent used clinically in rheumatoid arthritis and systemic lupus erythematosus, displayed a slightly improved activity (IC50 = 200 lM) compared to thioflavine T (IC50 = 230 lM). Uses: Anti-alzheimer agents; amyloid-β inhibitor. Synonyms: LY 53616; LY53616; LY-53616; Frentizole; 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenylurea; 7EY946394I; frentizole; mono-hydrate of frentizole; FRENTIZOLE; 26130-02-9; Frentizol; Compound 53616; MLS000555007; CHEMBL128988; UNII-7EY946394I; 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenylurea; NCGC00160657-01; SMR000147124; 1-(6-Methoxy-benzothiazol-2-yl)-3-phenyl-urea; DSSTox_CID_26279; DSSTox_RID_81505; 1-(6-methoxybenzo[d]thiazol-2-yl)-3-phenylurea; DSSTox_GSID_46279; CAS-26130-02-9; Frentizolum; Frenazole; AC1Q4EVH; Frentizole (USAN/INN); Opera_ID_1653; Frentizol [INN-Spanish]; Frentizolum [INN-Latin]; AC1L1PF2; Oprea1_516941; cid_33334; MLS001201824; Bio-0413; Frentizole [USAN:INN:BAN]; SCHEMBL599582; DTXSID5046279; HMS2233G12; HMS3370C02; ZINC8994439; Tox21_111964; 3684AH; BDBM50189352; STK078558; ZINC08994439; AKOS001049350; Tox21_111964_1; 7EY946394I; CS-0841; MCULE-7561551977; NCGC00160657-03; AK468739; DR001179; HE329695; HY-15374; LY 53616; ST50103599; 1-(6-Methoxy-2-benzothiazolyl)-3-phenylurea; 1-(6-methoxybenzothiazol-2-yl)-3-phenylurea; D00159; W-5046; Urea, N-(6-methoxy-2-benzothiazolyl)-N'-phenyl-; 3-(6-methoxy-1,3-benzothiazol-2-yl)-1-phenylurea; N-(6-methoxybenzothiazol-2-yl)(phenylamino)carboxamide; T0510-0233. CAS No. 26130-02-9. Molecular formula: C15H13N3O2S. Mole weight: 299.35.
PM-1
PM-1, a derivative of Thioflavin-T (ThT; HY-D0218), is a small but highly specific plasma membrane (PM) fluorescent dye for specific and long-time membrane imaging of living and fixed cells. PM-1 is embedded directly into the cell membrane and exhibits a very long retention time on the plasma membrane with a half-life of approximately 15 h. PM-1 can be used in combination with protein labeling probes to study ectodomain shedding and endocytosis processes of cell surface proteins [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 1449483-78-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156404.
RAGE Antagonist, FPS-ZM1
A blood-brain-barrier-permeant, non-toxic, tertiary amide compound that acts as a high affinity, potent, multimodal blocker of RAGE (Receptor for Advanced Glycation End products) V domain-mediated ligand binding (Ki = 25, 148, and 230nM, respectively, against Ab40, HMGB1, and S100B, binding to sRAGE). Blocks RAGE-mediated influx of Ab40 and Ab42 into the brain. Also shown to suppress Ab-RAGE induced NF-kB activation and NF-kB-dependent transcription of b-secretase. Daily treatment of APPsw/0 murine AD model (1mg/kg/d via i.p.) is reported to greatly reduce Thioflavin S-positive amyloid plaques in cortex and hippocampus (by 70 to 80%) and restore congnitive performance to the level of non-AD mice.CAS No:945714-67-0. Group: Biochemicals. Grades: Highly Purified. CAS No. 945714-67-0. Pack Sizes: 25mg. US Biological Life Sciences.
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