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Loganin is an iridoid glycoside that has been found in C. fructus and has diverse biological activities. It reduces hydrogen peroxide-induced apoptosis in SH-SY5Y cells when used at concentrations ranging from 0.25 to 12.5 µM. Loganin inhibits COX-1 activity (IC50 = 3.55 µM), as well as LPS-induced TNF-alpha formation (IC50 = 154.6 µM) in RAW 264.7 cells. In vivo, loganin (20 and 100 mg/kg) reduces food intake, blood glucose levels, and serum triglyceride levels, as well as increases serum HDL levels in db/db diabetic mice. It attenuates scopolamine-induced memory deficits in the Morris water maze and passive avoidance test in mice. Loganin (20 and 1,000 mg/kg) reduces serum and kidney advanced glycation end-product (AGE) and malondialdehyde (MDA) levels and improves renal function in a mouse model of diabetic nephropathy.Formal Name: 1-(beta-D-glucopyranosyloxy)-1S,4aS,5,6S,7R,7aS-hexahydro-6-hydroxy-7-methyl-cyclopenta[c]pyran-4-carboxylic acid, methyl ester. CAS Number: 18524-94-2. Synonyms: NSC 606403, 7-hydroxy-6-desoxy Verbenalin. Molecular Formula: C17H26O10. Formula Weight: 390.4. Purity: >98%. Formulation: (Request formulation change), A crystalline solid. Solubility: DMF: 15 mg/ml, DMSO: 10 mg/ml, PBS (pH 7.2): 10 mg/ml. lambdamax: 236 nm. SMILES: OC[C@H]1O[C@](O[C@@H]2OC=C(C(OC)=O)[C@]3([H])[C@@]2([H])[C@@H](C)[C@@H](O)C3)([H])[C@H](O)[C@@H](O)[C@@H]1O. InChi Code: InChI=1S/C17H26O10/c1-6-9(19)3-7-8(15(23)24-2)5-25-16(11(6)7)27-17-14(22)13(21)12(20)10(4-18)26-17/h5-7,9-14,16-22H,3-4H2,1-2H3/t6-,7+,9-,10+,11+,12+,13-,14+,16-,17-/m0/s1. InChi Key: AMBQHHVBBHTQBF-UOUCRYGSSA-N. Origin: Plant/Cornus.
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