Kuo CC - Search Results

1

Four new 6-nor5(6-->7)abeo-abietane type diterpenes and antitumoral cytotoxic diterpene constituents from the bark of Taiwania cryptomerioides.

Chang CI, Chang JY, Kuo CC, Pan WY, Kuo YH. Chang CI, et al. Among authors: kuo yh, kuo cc. Planta Med. 2005 Jan;71(1):72-6. doi: 10.1055/s-2005-837754. Planta Med. 2005. PMID: 15678377

2

2,2'-Diphenyl-1-picrylhydrazyl radical-scavenging active components from adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) hulls.

Kuo CC, Chiang W, Liu GP, Chien YL, Chang JY, Lee CK, Lo JM, Huang SL, Shih MC, Kuo YH. Kuo CC, et al. Among authors: kuo yh. J Agric Food Chem. 2002 Oct 9;50(21):5850-5. doi: 10.1021/jf020391w. J Agric Food Chem. 2002. PMID: 12358449

3

Antioxidative 7-oxodehydropodocarpane-type trinorditerpenes from the bark of Taiwania cryptomerioides.

Kuo YH, Chien SC, Kuo CC. Kuo YH, et al. Among authors: kuo cc. Planta Med. 2002 Nov;68(11):1020-3. doi: 10.1055/s-2002-35648. Planta Med. 2002. PMID: 12451494

4

Salvinal, a novel microtubule inhibitor isolated from Salvia miltiorrhizae Bunge (Danshen), with antimitotic activity in multidrug-sensitive and -resistant human tumor cells.

Chang JY, Chang CY, Kuo CC, Chen LT, Wein YS, Kuo YH. Chang JY, et al. Among authors: kuo yh, kuo cc. Mol Pharmacol. 2004 Jan;65(1):77-84. doi: 10.1124/mol.65.1.77. Mol Pharmacol. 2004. PMID: 14722239

5

Three new oleanane-type triterpenes from Ludwigia octovalvis with cytotoxic activity against two human cancer cell lines.

Chang CI, Kuo CC, Chang JY, Kuo YH. Chang CI, et al. Among authors: kuo yh, kuo cc. J Nat Prod. 2004 Jan;67(1):91-3. doi: 10.1021/np030267m. J Nat Prod. 2004. PMID: 14738395

6

A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells.

Juang SH, Pan WY, Kuo CC, Liou JP, Hung YM, Chen LT, Hsieh HP, Chang JY. Juang SH, et al. Among authors: kuo cc. Biochem Pharmacol. 2004 Jul 15;68(2):293-303. doi: 10.1016/j.bcp.2004.03.036. Biochem Pharmacol. 2004. PMID: 15194001

7

BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo.

Kuo CC, Hsieh HP, Pan WY, Chen CP, Liou JP, Lee SJ, Chang YL, Chen LT, Chen CT, Chang JY. Kuo CC, et al. Cancer Res. 2004 Jul 1;64(13):4621-8. doi: 10.1158/0008-5472.CAN-03-3474. Cancer Res. 2004. PMID: 15231674

8

Cytotoxic triterpenes from the aerial roots of Ficus microcarpa.

Chiang YM, Chang JY, Kuo CC, Chang CY, Kuo YH. Chiang YM, et al. Among authors: kuo yh, kuo cc. Phytochemistry. 2005 Feb;66(4):495-501. doi: 10.1016/j.phytochem.2004.12.026. Phytochemistry. 2005. PMID: 15694457

9

DNA repair enzyme, O6-methylguanine DNA methyltransferase, modulates cytotoxicity of camptothecin-derived topoisomerase I inhibitors.

Kuo CC, Liu JF, Chang JY. Kuo CC, et al. J Pharmacol Exp Ther. 2006 Feb;316(2):946-54. doi: 10.1124/jpet.105.095919. Epub 2005 Oct 28. J Pharmacol Exp Ther. 2006. PMID: 16258022

10

Structure-activity relationship studies of 3-aroylindoles as potent antimitotic agents.

Liou JP, Mahindroo N, Chang CW, Guo FM, Lee SW, Tan UK, Yeh TK, Kuo CC, Chang YW, Lu PH, Tung YS, Lin KT, Chang JY, Hsieh HP. Liou JP, et al. Among authors: kuo cc. ChemMedChem. 2006 Oct;1(10):1106-18. doi: 10.1002/cmdc.200600125. ChemMedChem. 2006. PMID: 16952120

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