SCOPUS 정보 검색 플랫폼

Organic Letters

Volumn 9, Issue 22, 2007, Pages 4579-4581

Chamobtusin A, a novel skeleton diterpenoid alkaloid from Chamaecyparis obtusa cv. tetragon

(5) Zhang, Yu Mei a Tan, Ning Hua a Lu, Yang b Chang, Ying b Jia, Rui Rui a

a KUNMING INSTITUTE OF BOTANY (China)

b INSTITUTE OF MATERIA MEDICA (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ANTINEOPLASTIC AGENT; CHAMOBTUSIN A; DITERPENE; UNCLASSIFIED DRUG;

ARTICLE; CHAMAECYPARIS; CHEMICAL STRUCTURE; CHEMISTRY; CLASSIFICATION; DOSE RESPONSE; HUMAN; IC 50; PLANT LEAF; TUMOR CELL LINE;

ALKALOIDS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL LINE, TUMOR; CHAMAECYPARIS; DITERPENES; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; INHIBITORY CONCENTRATION 50; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PLANT LEAVES;

EID: 35948946854 PISSN: 15237060 EISSN: None Source Type: Journal
DOI: 10.1021/ol702087h Document Type: Article

Times cited : (20)

References (19)

1
- 58149089446
- Science Press: China, Tomus 7, pp
- Delectis Florae Reipublicae Popularis Sinicae Agendae Academiae Sinicae Edita. Flora of China; Science Press: China, 1978; Tomus 7, pp 313-397.
- (1978) Flora of China , pp. 313-397
- Florae Reipublicae, D.¹ Sinicae, P.² Academiae, A.³ Edita, S.⁴

2
- 0030049272
- Hieda, T.; Tazaki, M.; Morishita, Y.; Aoki, T. Phytochemistry 1996, 42, 159-162.
- (1996) Phytochemistry , vol.42 , pp. 159-162
- Hieda, T.¹ Tazaki, M.² Morishita, Y.³ Aoki, T.⁴

3
- 0035897222
- Kuo, Y. H.; Chen, C. H. Tetrahedron Lett. 2001, 42, 2985-2986.
- (2001) Tetrahedron Lett , vol.42 , pp. 2985-2986
- Kuo, Y.H.¹ Chen, C.H.²

4
- 0035903943
- Kuo, Y. H.; Chen, C. H.; Chiang, Y. M. Tetrahedron Lett. 2001, 42, 6731-6735.
- (2001) Tetrahedron Lett , vol.42 , pp. 6731-6735
- Kuo, Y.H.¹ Chen, C.H.² Chiang, Y.M.³

5
- 0000092314
- Gadek, P. A.; Quinn, C. J. Phytochemistry 1987, 26, 2551-2552.
- (1987) Phytochemistry , vol.26 , pp. 2551-2552
- Gadek, P.A.¹ Quinn, C.J.²

6
- 33846625183
- Chien, S. C.; Chang, J. Y.; Kuo, C. C.; Hsieh, C. C. Tetrahedron Lett. 2007, 48, 1567-1569.
- (2007) Tetrahedron Lett , vol.48 , pp. 1567-1569
- Chien, S.C.¹ Chang, J.Y.² Kuo, C.C.³ Hsieh, C.C.⁴

7
- 33745114422
- Xu, J. F.; Cao, D. H.; Tan, N. H.; Liu, Z. L.; Zhang, Y. M.; Yang, Y. B. J. Asian Nat. Prod. Res. 2006, 8, 181-185.
- (2006) J. Asian Nat. Prod. Res , vol.8 , pp. 181-185
- Xu, J.F.¹ Cao, D.H.² Tan, N.H.³ Liu, Z.L.⁴ Zhang, Y.M.⁵ Yang, Y.B.⁶

8
- 4644349886
- Barrero, A. F.; Quilez del Moral, J. F.; Mar Herrador, M.; Akssira, M.; Bennamara, A.; Akkad, S.; Aitigri, M. Phytochemistry 2004, 65, 2507-2515.
- (2004) Phytochemistry , vol.65 , pp. 2507-2515
- Barrero, A.F.¹ Quilez del Moral, J.F.² Mar Herrador, M.³ Akssira, M.⁴ Bennamara, A.⁵ Akkad, S.⁶ Aitigri, M.⁷

9
- 33751278908
- Okasaka, M.; Takaishi, Y.; Kashiwada, Y.; Kodzhimatov, O.; Ashurmetov, O.; Lin, A. J.; Consentino, L. M.; Lee, K. H. Phytochemistry 2006, 67, 2635-2640.
- (2006) Phytochemistry , vol.67 , pp. 2635-2640
- Okasaka, M.¹ Takaishi, Y.² Kashiwada, Y.³ Kodzhimatov, O.⁴ Ashurmetov, O.⁵ Lin, A.J.⁶ Consentino, L.M.⁷ Lee, K.H.⁸

10
- 33845984557
- Smith, E. C. J.; Williamson, E. M.; Wareham, N.; Kaatz, G. W.; Gibbons, S. Phytochemistry 2007, 68, 210-217.
- (2007) Phytochemistry , vol.68 , pp. 210-217
- Smith, E.C.J.¹ Williamson, E.M.² Wareham, N.³ Kaatz, G.W.⁴ Gibbons, S.⁵

11
- 35948942026
- +.
- +.

12
- 35948929149
- A pale yellow crystal of dimensions 0.50 x 0.80 x 0.04 mm was used for X-ray diffraction on a MAC DIP-2030K diffractometer with Mo Ka radiation and graphite monochromator by maximum 2θ value of 50.0°. The total number of independent reflections was 3714, of which 3306 were observed, F|2 ≥ 2σ(|F|2), Crystal data: molecular formula (C20H31O2N 1)· (H2O)2.5, M, 317.48 (excluded the solvent, orthorhombic system, space group: C2, a, 23.563(1) Å, b, 8.728(1) Å c, 19.397(1) Å, β, 90.48(1)°, V, 3989.0(5) Å3, Z, 8, d, 1.132 g/cm3. The structure was solved by the direct method (SHELXs-9713) and expanded using difference Fourier techniques, refined by the full-matrix least-squares method NOMCSDP14, Hydrogen atoms were fixed at
- 2), S = 1.053. Crystallographic data (excluding structure factors) for the structures in this paper, have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 651044. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44 (0) 1223-336-033 or e-mail: deposit@ccdc.cam.ac.uk).

13
- 0004150157
- University of Gottingen: Germany
- Sheldrick, G. M. SHELX-97, Program for Crystal Structure Refinement; University of Gottingen: Germany, 1997.
- (1997) SHELX-97, Program for Crystal Structure Refinement
- Sheldrick, G.M.¹

14
- 0000869023
- Lu, Y.; Wu, B. M. Chinese Chem. Lett. 1992, 3, 637-640.
- (1992) Chinese Chem. Lett , vol.3 , pp. 637-640
- Lu, Y.¹ Wu, B.M.²

15
- 0027508436
- Tawara, J. N.; Blockhin, A.; Foderaro, T. A.; Stermitz, F. R. J. Org. Chem. 1993, 58, 4813-4818.
- (1993) J. Org. Chem , vol.58 , pp. 4813-4818
- Tawara, J.N.¹ Blockhin, A.² Foderaro, T.A.³ Stermitz, F.R.⁴

16
- 0032984987
- Tawara, J. N.; Lorenz, D.; Stermitz, F. R. J. Nat. Prod. 1999, 62, 321-323.
- (1999) J. Nat. Prod , vol.62 , pp. 321-323
- Tawara, J.N.¹ Lorenz, D.² Stermitz, F.R.³

17
- 0036899892
- Tan, N.; Kaloga, M.; Radtke, O. A.; Kiderlen, A. F.; Öksüz, S.; Ulubelen, A.; Kolodziej, H. Phytochemistry 2002, 61, 881-884.
- (2002) Phytochemistry , vol.61 , pp. 881-884
- Tan, N.¹ Kaloga, M.² Radtke, O.A.³ Kiderlen, A.F.⁴ Öksüz, S.⁵ Ulubelen, A.⁶ Kolodziej, H.⁷

18
- 33745121907
- Aoyagi, Y.; Takahashi, Y.; Satake, Y.; Takeya, K.; Aiyama, R.; Matsuzaki, T.; Hashimoto, S.; Kurihara, T. Bioorg. Med. Chem. 2006, 14, 5285-5291.
- (2006) Bioorg. Med. Chem , vol.14 , pp. 5285-5291
- Aoyagi, Y.¹ Takahashi, Y.² Satake, Y.³ Takeya, K.⁴ Aiyama, R.⁵ Matsuzaki, T.⁶ Hashimoto, S.⁷ Kurihara, T.⁸

19
- 15944413480
- Son, K. H.; Oh, H. M.; Choi, S. K.; Han, D. C.; Kwon, B. M. Bioorg. Med. Chem. Lett. 2005, 15, 2019-2021.
- (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 2019-2021
- Son, K.H.¹ Oh, H.M.² Choi, S.K.³ Han, D.C.⁴ Kwon, B.M.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.