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1-[(3R,3aS,5aR,6R,9bS)-6-Hydroxy-5a-methyl-9-methylene-2-oxoperhydronaphtho[1,2-b]furan-3-ylmethyl]pyrrolidine-2(S)-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148225-52-9

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148225-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148225-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,2,2 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148225-52:
(8*1)+(7*4)+(6*8)+(5*2)+(4*2)+(3*5)+(2*5)+(1*2)=129
129 % 10 = 9
So 148225-52-9 is a valid CAS Registry Number.

148225-52-9Downstream Products

148225-52-9Relevant academic research and scientific papers

Absolute stereostructures and syntheses of saussureamines A, B, C, D and E, amino acid-sesquiterpene conjugates with gastroprotective effect, from the roots of Saussurea lappa

Matsuda, Hisashi,Kageura, Tadashi,Inoue, Yasunao,Morikawa, Toshio,Yoshikawa, Masayuki

, p. 7763 - 7777 (2007/10/03)

From the methanolic extract of the dried roots of Saussurea lappa Clarke, Saussureae Radix, five amino acid-sesquiterpene conjugates, saussureamines A, B, C, D and E, were isolated together with a lignan glycoside, (-)-massoniresinol 4-O-β-D-glucopyranoside. Their stereostructures were determined on the basis of chemical and physicochemical evidence. In addition, saussureamines and the related amino acid-sesquiterpene conjugates were synthesized using a Michael type addition reaction of amino acid to the α-methylene-γ-lactone moiety of sesquiterpenes. Saussureamines A, B and C, costunolide and dehydrocostus lactone showed a gastroprotective effect on acidified ethanol-induced gastric mucosal lesions in rats. Saussureamines A also exhibited an inhibitory effect on gastric mucosal lesions induced by water-immersion stress in mice. (C) 2000 Elsevier Science Ltd.

Saussureamines A, B, C, D, and E, new anti-ulcer principles from Chinese Saussureae radix

Yoshikawa,Hatakeyama,Inoue,Yamahara

, p. 214 - 216 (2007/10/02)

Five new amino acid-sesquiterpene adducts, saussureamines A, B, C, D, and E, were isolated from Chinese Saussureae Radix, the dried root of Saussurea lappa Clarke, together with a new lignan glycoside, (-)-massoniresinol 4-O-β-D-glucopyranoside. Their structures were determined on the basis of chemical and physicochemical evidence. Among of these compounds, saussureamines A, B, C showed anti-ulcer effect on HCl/ethanol-induced lesions in rats, and saussureamine A also exhibited an inhibitory activity on stress-induced ulcer formation in mice. During the course of these studies, facile conversion from sesquiterpene having an α-methylene γ-lactone function to amino acid-sesquiterpene adduct has been accomplished by means of Michael type addition reaction.

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