Page 64 - วารสารกรมการแพทย์แผนไทยฯ ปีที่ 11 ฉบับที่ 3
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Journal of Thai Traditional & Alternative Medicine  Vol. 11 No. 3 September-December 2013 273



               227 nm, EI-MS: m/z (relative intensity, %);   °—¥À¬“∫‡∂“«—≈¬å‡ª√’¬ß¥â«¬ 50% ‡Õ∑“πÕ≈ ¥â«¬
               [C H O ] 279.47 [M+Na] (65). genistein 7-  «‘∏’‚§√¡“‚∑°√“øï ¡√√∂π– Ÿßæ∫«à“¡’Õß§åª√–°Õ∫
                11 12 7
               O-α-rhamnosyl(1→6)-β-glucopyranoside (2):  ∑“߇§¡’√«¡ª√–¡“≥ 13 ™π‘¥ ‚¥¬æ∫ genistein
               λ    = 261 nm, EI-MS : m/z (relative inten-  7-O-α-rhamnosyl (1→6)-β-glucopyranoside (2)
                max
               sity, %) [C H O ], 601.55 [M+Na] (60),    ‡ªìπÕß§åª√–°Õ∫À≈—°∑’Ë retention time ‡∑à“°—∫ 8.75
                         27 31 14
               579.59(40), 433.63 (30), 271.58 (100) ‚¥¬ Ÿμ√  π“∑’ ·≈– piscidic acid (1) ‡ªìπÕß§åª√–°Õ∫√Õß∑’Ë
               ‚§√ß √â“ß∑“߇§¡’¢Õß “√∑—Èß Õß™π‘¥· ¥ß„π√Ÿª∑’Ë 3  retention time ‡∑à“°—∫ 1.45 π“∑’ (√Ÿª∑’Ë 4) º≈
               ®“°º≈°“√«‘‡§√“–ÀåÕß§åª√–°Õ∫∑“߇§¡’¢Õß “√  °“√»÷°…“ƒ∑∏‘Ϭ—∫¬—È߇Õπ‰´¡å COX æ∫«à“ 1 ‰¡à¡’


                                      1
               μ“√“ß∑’Ë 4 ¢âÕ¡Ÿ≈ 500 MHz H -NMR ¢Õß 2 ‡ª√’¬∫‡∑’¬∫°—∫ genistein 7-O-α-rhamnosy (1  → 6)-β-
                                   5
                       glucopyranoside
                                                                      δ  (ppm) „π d -DMSO ¢Õß
                                                                       H         6
                μ”·Àπàß‚ª√μÕπ      δ  (ppm) „π d -DMSO ¢Õß 2          genistein 7-O-α-rhamnosyl
                                    H
                                              6
                                                                                           5
                                                                     (1 → 6)-β-glucopyranoside
                      2                  8.27 (1H, s)                      8.40 (1H, s)
                      5                12.83 (1H, br s)                   12.88 (1H, br s)
                      6               6.44 (1H, d, J = 2.1)             6.44 (1H, d, J = 2.1)
                      8               6.73 (1H, d, J = 1.8)             6.73 (1H, d, J = 2.1)
                     2'              7.40 (2H, d, J = 8.55)             7.40 (2H, d, J = 8.5)
                     3'               6.83 (2H, d, J = 8.8)             6.83 (2H, d, J = 8.5)
                     4'                 9.65 (1H, br s)                   9.65 (1H, br s)
                     5'               6.83 (2H, d, J = 8.8)             6.83 (2H, d, J = 8.5)
                     6'              7.40 (2H, d, J = 8.55)             7.40 (2H, d, J = 8.5)
                     1''              4.55 (1H, d, J = 7.3)             5.18 (1H, d, J = 6.9)
                     2''                     -*                                -*
                     3''                     -*                                -*
                     4''                     -*                                -*
                     5''                     -*                                -*
                     6''         3.90 (1H, dd, J = 10.99, 1.53),     3.91 (1H, dd, J = 14.2, 3.2),
                                         3.47 (1H, m)                  3.47 (1H, dd, 14.2, 3.2)
                     1'''                4.54 (1H, s)                      4.62 (1H, s)
                     2'''                    -*                                -*
                     3'''                    -*                                -*
                     4'''                    -*                                -*
                     5'''                    -*                                -*
                     6'''                    -*                                -*
               *signals due to most sugar protons were not given
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