SCOPUS 정보 검색 플랫폼

Journal of Natural Products

Volumn 73, Issue 11, 2010, Pages 1743-1750

Synthesis and biological evaluation of oleanolic acid derivatives as inhibitors of protein tyrosine phosphatase 1B

(6) Qian, Shan a,b Li, Haijiao b Chen, Yin c Zhang, Weiyu c Yang, Shengyong b Wu, Yong b

a XIHUA UNIVERSITY (China)

b SICHUAN UNIVERSITY (China)

c Drug Screening Center (China)

Author keywords

[No Author keywords available]

Indexed keywords

3 OXO 12 ENE 28 BROMO OLEANANE; 3 OXO 12 ENOLEAN 28 OIC ACID TRIFLUOROMETHANESULFONATE; 3 OXO 28 (ADIPOYL 4')ERYTHRANE; 3 OXO 28 (BENZYLADIPOYL 4')ERYTHRANE; 3 OXO 28 (BENZYLGLUTARYL 4')ERYTHRANE; 3 OXO 28 (BENZYLMALONYL 4')ERYTHRANE; 3 OXO 28 (BENZYLPHTHALOYL 4')ERYTHRANE; 3 OXO 28 (BENZYLSEBACOYL 4')ERYTHRANE; 3 OXO 28 (BENZYLSUCCINYL 4' )ERYTHRANE; 3 OXO 28 (GLUTARYL 4')ERYTHRANE; 3 OXO 28 (MALONYL 4')ERYTHRANE; 3 OXO 28 (PHTHALOYL 4')ERYTHRANE; 3 OXO 28 (SEBACOYL 4')ERYTHRANE; 3 OXO 28 (SUCCINYL 4')ERYTHRANE; 3 OXO ERYTHRODIOL; 3 OXO OLEAN 12ALPHA HYDROXY 28 OIC ACID GAMMA LACTONE; 3 SPIRO[1',2']DIOXOLANERYTHRODIOL; 3BETA (2' CARBOXYBENZOYL) 12ALPHA HYDROXY 28 OIC ACID GAMMA LACTONE; ENZYME INHIBITOR; OLEAN 12 EN 28 CARBOXY 3 OIC ACID EPSILON LACTONE; OLEAN 12 EN 4 HYDROXY 3,28 DIOIC ACID; OLEAN 12 ENE 2 FORMYL 28 CARBOXY 3 OIC ACID METHYL ESTER; OLEAN 12 OXO 28 METHOXYCARBONYL 3 OIC ACID EPSILON LACTONE; OLEAN 12 OXO 4 HYDROXY 3 CARBOXY 28 OIC ACID GAMMA LACTONE; OLEAN 12 OXO 4 HYDROXY 3,28 DIOIC ACID; OLEAN 12ALPHA HYDROXY 3 EPSILON LACTON 28 OIC ACID GAMMA LACTONE; OLEAN 4,12ALPHA DIHYDROXY 3 CARBOXY 28 OIC ACID GAMMA LACTONE; OLEANOLIC ACID DERIVATIVE; PROTEIN TYROSINE PHOSPHATASE 1B; UNCLASSIFIED DRUG;

ARTICLE; BAEYER VILLIGER REACTION; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ACTIVITY; DRUG OXIDATION; DRUG STRUCTURE; DRUG SYNTHESIS; IC 50; MOLECULAR DOCKING; PROTEIN PHOSPHORYLATION; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION;

DIABETES MELLITUS; DRUGS, CHINESE HERBAL; ESCHERICHIA COLI; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OBESITY; OLEANOLIC ACID; PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 1; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 78650191760 PISSN: 01633864 EISSN: 15206025 Source Type: Journal
DOI: 10.1021/np100064m Document Type: Article

Times cited : (59)

References (19)

1
- 0024287614
- Tonks, N. K., Diltz, C. D., and Fischer, E. H. J. Biol. Chem. 1988, 263, 6731-6737
- (1988) J. Biol. Chem. , vol.263 , pp. 6731-6737
- Tonks, N.K.¹ Diltz, C.D.² Fischer, E.H.³

2
- 0034308201
- Kennedy, B. P. and Ramachandran, C. Biochem. Pharmacol. 2000, 60, 877-883
- (2000) Biochem. Pharmacol. , vol.60 , pp. 877-883
- Kennedy, B.P.¹ Ramachandran, C.²

3
- 0028880718
- Barford, D., Jia, Z., and Tonks, N. K. Nat. Struct. Biol. 1996, 2, 1043-1053
- (1996) Nat. Struct. Biol. , vol.2 , pp. 1043-1053
- Barford, D.¹ Jia, Z.² Tonks, N.K.³

4
- 0037317489
- Zhang, Z. Y. and Lee, S. Y. Expert Opin. Investig. Drugs 2003, 12, 223-233
- (2003) Expert Opin. Investig. Drugs , vol.12 , pp. 223-233
- Zhang, Z.Y.¹ Lee, S.Y.²

5
- 5744220107
- Pei, Z. H., Liu, G., Lubben, T. H., and Szczepankiewicz, B. G. Curr. Pharm. Des. 2004, 10, 3481-3504
- (2004) Curr. Pharm. Des. , vol.10 , pp. 3481-3504
- Pei, Z.H.¹ Liu, G.² Lubben, T.H.³ Szczepankiewicz, B.G.⁴

6
- 51449111044
- Zhang, Y. N., Zhang, W., Hong, D., Shi, L., Shen, Q., Li, J. Y., Li, J., and Hua, L. H. Bioorg. Med. Chem. 2008, 16, 8697-8705
- (2008) Bioorg. Med. Chem. , vol.16 , pp. 8697-8705
- Zhang, Y.N.¹ Zhang, W.² Hong, D.³ Shi, L.⁴ Shen, Q.⁵ Li, J.Y.⁶ Li, J.⁷ Hua, L.H.⁸

7
- 0026525833
- Singh, G. B., Singh, S., Bani, S., Gupta, B. D., and Banerjee, S. K. J. Pharm. Pharmacol. 1992, 44, 456-458
- (1992) J. Pharm. Pharmacol. , vol.44 , pp. 456-458
- Singh, G.B.¹ Singh, S.² Bani, S.³ Gupta, B.D.⁴ Banerjee, S.K.⁵

8
- 0031024074
- Hsu, H. Y., Yang, J. J., and Lin, C. C. Cancer Lett. 1997, 111, 7-13
- (1997) Cancer Lett. , vol.111 , pp. 7-13
- Hsu, H.Y.¹ Yang, J.J.² Lin, C.C.³

9
- 0029617925
- Liu, J., Liu, Y., and Parkinson, A. J. Pharmacol. Exp. Ther. 1995, 275, 768-774
- (1995) J. Pharmacol. Exp. Ther. , vol.275 , pp. 768-774
- Liu, J.¹ Liu, Y.² Parkinson, A.³

10
- 49949144833
- Tursch, B., Savoir, R., Ottinger, R., and Chiurdoglu, G. Tetrahedron Lett. 1967, 8, 539-543
- (1967) Tetrahedron Lett. , vol.8 , pp. 539-543
- Tursch, B.¹ Savoir, R.² Ottinger, R.³ Chiurdoglu, G.⁴

11
- 0000820093
- Huneck, S. Tetrahedron 1963, 19, 479-482
- (1963) Tetrahedron , vol.19 , pp. 479-482
- Huneck, S.¹

12
- 45749110639
- Wen, X. A., Sun, H. B., Liu, J., Cheng, K. G., Zhang, P., Zhang, L. Y., Hao, J., Zhang, L. Y., Ni, P. Z., Zographos, S. E., Leonidas, D. D., Alexacou, K. M., Gimisis, T., Hayes, J. M., and Oikonomakos, N. G. J. Med. Chem. 2008, 51, 3540-3554
- (2008) J. Med. Chem. , vol.51 , pp. 3540-3554
- Wen, X.A.¹ Sun, H.B.² Liu, J.³ Cheng, K.G.⁴ Zhang, P.⁵ Zhang, L.Y.⁶ Hao, J.⁷ Zhang, L.Y.⁸ Ni, P.Z.⁹ Zographos, S.E.¹⁰ Leonidas, D.D.¹¹ Alexacou, K.M.¹² Gimisis, T.¹³ Hayes, J.M.¹⁴ Oikonomakos, N.G.¹⁵

13
- 0037030814
- Ali, M. S., Jahangir, M., Hussan, S. S., and Choudhary, M. I. Phytochemistry 2002, 60, 295-299
- (2002) Phytochemistry , vol.60 , pp. 295-299
- Ali, M.S.¹ Jahangir, M.² Hussan, S.S.³ Choudhary, M.I.⁴

14
- 33646027276
- Chen, J., Liu, J., Zhang, L. Y., Wu, G. Z., Hua, W. Y., Wu, X. M., and Sun, H. B. Bioorg. Med. Chem. Lett. 2006, 16, 2915-2919
- (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 2915-2919
- Chen, J.¹ Liu, J.² Zhang, L.Y.³ Wu, G.Z.⁴ Hua, W.Y.⁵ Wu, X.M.⁶ Sun, H.B.⁷

15
- 29544449934
- Wen, X. A., Zhang, P., Liu, J., Zhang, L. Y., Wu, X. M., Ni, P. Z., and Sun, H. B. Bioorg. Med. Chem. Lett. 2006, 16, 722-726
- (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 722-726
- Wen, X.A.¹ Zhang, P.² Liu, J.³ Zhang, L.Y.⁴ Wu, X.M.⁵ Ni, P.Z.⁶ Sun, H.B.⁷

16
- 70149111759
- (ISSN: 1006-0103, in Chinese)
- Jiang, Q. L., Wu, L. Y., and Wu, Y. West China J. Pharm. Sci. 2005, 20, 12-14 (ISSN: 1006-0103, in Chinese)
- (2005) West China J. Pharm. Sci. , vol.20 , pp. 12-14
- Jiang, Q.L.¹ Wu, L.Y.² Wu, Y.³

17
- 0029066496
- Jia, Z., Barford, D., Flint, A. J., and Tonks, N. Science 1995, 268, 1754-1758
- (1995) Science , vol.268 , pp. 1754-1758
- Jia, Z.¹ Barford, D.² Flint, A.J.³ Tonks, N.⁴

18
- 32944477948
- Moretto, A. F., Kirincich, S. J., Xu, W. X., Smith, M. J., Wan, Z. K., Wilson, D. P., Follows, B. C., Binnun, E., Joseph-McCarthy, D., Foreman, K., Erbe, D. V., Zhang, Y. L., Tam, S. K., Tama, S. Y., and Lee, J. Bioorg. Med. Chem. 2006, 14, 2162-2177
- (2006) Bioorg. Med. Chem. , vol.14 , pp. 2162-2177
- Moretto, A.F.¹ Kirincich, S.J.² Xu, W.X.³ Smith, M.J.⁴ Wan, Z.K.⁵ Wilson, D.P.⁶ Follows, B.C.⁷ Binnun, E.⁸ Joseph-Mccarthy, D.⁹ Foreman, K.¹⁰ Erbe, D.V.¹¹ Zhang, Y.L.¹² Tam, S.K.¹³ Tama, S.Y.¹⁴ Lee, J.¹⁵

19
- 0033578739
- Konoike, T., Araki, Y., and Kanda, Y. Tetrahedron Lett. 1999, 40, 6971-6974
- (1999) Tetrahedron Lett. , vol.40 , pp. 6971-6974
- Konoike, T.¹ Araki, Y.² Kanda, Y.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.