Dehydrotrametenonic Acid and Dehydroeburiconic Acid fromPoria cocosand Their Inhibitory Effects on Eukaryotic DNA Polymerase α and β

Author:

AKIHISA Toshihiro,MIZUSHINA Yoshiyuki,UKIYA Motohiko,OSHIKUBO Manabu,KONDO Seizo,KIMURA Yumiko,SUZUKI Takashi,TAI Takaaki

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

Reference5 articles.

1. 1) Zhong Shan Medical College, Clinical Application of Chinese Medicine, Guang Dong People’s Publisher, p. 136 (1975).

2. 8) Dehydrotrametenonic Acid (1). colorless needles from MeOH, mp 233–235°C. [α]D25+14.8° (c0.35, CHCl3). UV λmax(EtOH) nm: 236, 243, 252. IR νmax(KBr) cm−1: 1713, 1698, 1656, 813.13C- and1H-NMR, see Table 1. EIMSm⁄z: 452 (M+) (100), 437 (24), 434 (9), 370 (11), 311 (27), 309 (40), 270 (32), 269 (38), 257 (14), 255 (12), 244 (20), 229 (8), 69 (25). HREIMSm⁄z(M+): Calcd. for C30H44O3: 452.3287, Found: 452.3290.

3. 9) Dehydroeburiconic acid (2). colorless needles from MeOH, mp 237–239°C;1H-NMR δH(C5D5N): 1.00 (3H, s, H-18), 1.03 (3H, s, H-30), 1.03 and 1.04 (both 3H, two d, bothJ=7.0 Hz, H-26 and H-27), 1.07 (3H, s, H-29), 1.13 (3H, s, H-19), 1.14 (3H, s, H-28), 4.90 and 4.94 (both 1H, two s, H-241), 5.34 (1H, br s, H-11), 5.58 (1H, br d,J=5.9 Hz, H-7). EIMSm⁄z: 466 (M+) (100), 451 (22), 439 (7), 423 (9), 370 (8), 309 (68), 295 (28), 270 (24), 269 (37), 257 (16), 255 (12), 244 (12), 229 (9).

4. 11) Goad, L. J., and Akihisa, T. “Analysis of Sterols”, Blackie Academic & Professional, London, pp. 152–196 (1997).

5. 12) Tai, T. “On the Constituents ofPoria cocosWOLF”, Dissertation, Kobe-Gakuin University, Kobe, p. 86 (1996).

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