176 Publications (Page 5 of 8)
2002
Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro.
Perchellet, Elisabeth M⋅Sperfslage, Bonnie J⋅Wang, Yang⋅Huang, Xiaodong⋅Tamura, Masafumi⋅Hua, Duy H and Perchellet, Jean Pierre H
Anti-cancer drugs, vol. 13, (no. 6), pp. 567-81, 2002/Jul. | Journal Article
 
Induction of poly(ADP-ribose) polymerase-1 cleavage by antitumor triptycene bisquinones in wild-type and daunorubicin-resistant HL-60 cell lines.
Wang, Yang⋅Perchellet, Elisabeth M⋅Tamura, Masafumi⋅Hua, Duy H and Perchellet, Jean Pierre H
Cancer letters, vol. 188, (no. 1-2), pp. 73-83, 2002/Dec/15. | Journal Article
 
Novel tricyclic pyrone compounds prevent intracellular APP C99-induced cell death.
Jin, Lee Way⋅Hua, Duy H⋅Shie, Feng-Shiun⋅Maezawa, Izumi⋅Sopher, Bryce and Martin, George M
Journal of molecular neuroscience : MN. , vol. 19, (no. 1-2), pp. 57-61, 2002 Aug-Oct. | Journal Article
 
Syntheses and bioactivities of substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetrones. Unusual reactivities with amines.
Hua, Duy H⋅Tamura, Masafumi⋅Huang, Xiaodong⋅Stephany, Heidi A⋅Helfrich, Brian A⋅Perchellet, Elisabeth M⋅Sperfslage, Bonnie J⋅Perchellet, Jean-Pierre⋅Jiang, Suping⋅Kyle, Dennis E and Chiang, Peter K
The Journal of organic chemistry, vol. 67, (no. 9), pp. 2907-12, 2002/May/3. | Journal Article
2001
2,4,6‐Tris(1′‐phenyl­thio‐1‐ferrocenyl)­boroxin
Hua, Duy H.⋅McGill, James W.⋅Robinson, Paul D. and Meyers, Cal Y.
Acta crystallographica. Section E, Structure reports online, vol. 57, (no. 9), pp. m415, September 2001. | Journal Article
 
2‐Chloro‐2‐propyl mesityl sulfone
Hua, Duy H.⋅Meyers, Cal Y.⋅Hou, Yuqing and Robinson, Paul D.
Acta crystallographica. Section E, Structure reports online, vol. 57, (no. 7), pp. o589, July 2001. | Journal Article
 
A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines.
Wang, B⋅Wu, M⋅Perchellet, E M⋅McIlvain, C J⋅Sperfslage, B J⋅Huang, X⋅Tamura, M⋅Stephany, H A⋅Hua, Duy H and Perchellet, J P
International journal of oncology, vol. 19, (no. 6), pp. 1169-78, 2001/Dec. | Journal Article
 
ChemInform Abstract: Palladium-Mediated Ring Closure Reactions. Facile Syntheses of Enantiopure Bicyclic and Tricyclic Alkenones
Hua, Duy H.⋅Takasu, Kiyosei⋅Huang, Xiaodong⋅Millward, Gail S.⋅Chen, Yi and Fan, Jingmei
ChemInform, vol. 32, (no. 2), pp. no, 2001-01-09. | Journal Article
 
Resolution of 8′-alkoxy- and hydroxy-1,1′-binaphthalen-8-ols
Hua, Duy H.⋅Nguyen, Trieu X.C.⋅McGill, James W.⋅Chen, Yi and Robinson, Paul D.
Tetrahedron: asymmetry, vol. 12, (no. 14), pp. 2004, 2001-08-14. | Journal Article
 
Short syntheses of 8-substituted 8′-[1-(1′-phenylthio)ferrocenyl]-1,1′-binaphthyls from Suzuki coupling reactions. A strategy for generating new chiral ligands and charge-transfer complexes
Hua, Duy H⋅McGill, James W⋅Ueda, Masato and Stephany, Heidi A
Journal of organometallic chemistry, vol. 637, pp. 836, 2001-12-03. | Journal Article
 
Synthesis and evaluation of novel aldose reductase inhibitors: Effects on lens protein kinase Cgamma.
Lewis, S⋅Karrer, J⋅Saleh, S⋅Chan, X⋅Tan, Z⋅Hua, Duy H⋅McGill, J⋅Pang, Y. P.⋅Fenwick, B⋅Brightman, A and Takemoto, D
Molecular vision, vol. 7, pp. 164-71, 2001/Jul/18. | Journal Article
 
Synthetic 1,4-anthracenediones, which block nucleoside transport and induce DNA fragmentation, retain their cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines.
Wu, M⋅Wang, B⋅Perchellet, E M⋅Sperfslage, B J⋅Stephany, H A⋅Hua, Duy H and Perchellet, Jean Pierre H
Anti-cancer drugs, vol. 12, (no. 10), pp. 807-19, 2001/Nov. | Journal Article
2000
1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro.
Perchellet, E M⋅Magill, M J⋅Huang, X⋅Dalke, D M⋅Hua, Duy H and Perchellet, Jean Pierre H
Anti-cancer drugs, vol. 11, (no. 5), pp. 339-52, 2000/Jun. | Journal Article
 
cis, cis, cis-Tetramethyl 1,2,4,5-cyclohexanetetracarboxylate
ROBINSON, Paul D⋅HUA, Duy H⋅FAN, JINGMEI⋅LIU, LANZHU⋅MCGILL, James W⋅ARSHID, Mohammed and MEYERS, Cal Y
Acta crystallographica. Section C, Crystal structure communications, vol. 56, (no. 12), pp. 1472, 2000-12-01. | Journal Article
 
Palladium-Mediated Ring Closure Reactions. Facile Syntheses of Enantiopure Bicyclic and Tricyclic Alkenones
Hua, D.H.⋅Hua, Duy H⋅Takasu, K.⋅Takasu, Kiyosei⋅Huang, Xiaodong⋅Huang, X.⋅Millward, Gail S⋅Millward, G.S.⋅Chen, Yi⋅Chen, Y.⋅Fan, Jingmei and Fan, J.
Tetrahedron, vol. 56, (no. 38), pp. 7398, 2000-09-15. | Journal Article
1999
6,7,8,9-Tetrahydro-3-methyl-1H-pyrano-[4,3-b]quinolin-1-one.
Hua, Duy H⋅Chen, Y⋅Sin, H S⋅Robinson, P D⋅Meyers, C Y⋅Perchellet, E M⋅Perchellet, J P⋅Chiang, P K and Biellmann, J F
Acta crystallographica. Section C, Crystal structure communications, vol. 55 ( Pt 10), pp. 1698-701, 1999/Oct/15. | Journal Article
 
ChemInform Abstract: N-Alkylidenesulfinamides
Hua, Duy H.⋅Chen, Yi and Millward, Gail S.
ChemInform, vol. 30, (no. 25), pp. no, 1999-06-22. | Journal Article
 
N-Alkylidenesulfinamides
Hua, Duy H.⋅Chen, Yi and Millward, Gail S.
Sulfur reports, vol. 21, (no. 3), pp. 239, 2/1/1999. | Journal Article
 
Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivo
Perchellet, EM⋅Ladesich, JB⋅Magill, MJ⋅Chen, Yi⋅Hua, Duy H and Perchellet, J-P
Anti-Cancer Drugs, vol. 10, (no. 5), pp. 489-504, 1999. | Journal Article
 
Triptycenes: a novel synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro
Perchellet, EM⋅Magill, MJ⋅Huang, Xiaodong⋅Brantis, CE⋅Hua, Duy H and Perchellet, J-P
Anti-Cancer Drugs, vol. 10, (no. 8), pp. 749-766, 1999. | Journal Article
1998
Antitumor activity of tricyclic pyrone analogs, a new synthetic class of microtubule de-stabilizing agents, in the murine EMT-6 mammary tumor cell line in vitro
Perchellet, EM⋅Ladesich, JB⋅Chen, Yi⋅Sin, Hong-Sig⋅Hua, Duy H⋅Kraft, Susan L and Perchellet, J-P
Anti-Cancer Drugs, vol. 9, (no. 6), pp. 565-576, 1998. | Journal Article
 
Chiral sulfur-containing 1,2-disubstituted ferrocenes
Lagneau, N.M.⋅Lagneau, Nadege M.⋅Chen, Yi⋅Chen, Y.⋅Robben, P.M.⋅Robben, Paul M.⋅Sin, Hong-Sig⋅Sin, H.-S.⋅Takasu, K.⋅Takasu, Kiyosei⋅Chen, J.-S.⋅Chen, Jin-Shan⋅Robinson, Paul D.⋅Robinson, P.D.⋅Hua, Duy H. and Hua, D.H.
Tetrahedron, vol. 54, (no. 26), pp. 7334, 1998-06-25. | Journal Article
 
Tricyclic pyrone analogs: a new class of microtubule-disrupting anticancer drugs effective against murine leukemia cells in vitro.
Newell, S W⋅Perchellet, E M⋅Ladesich, J B⋅Freeman, Jonathan A⋅Chen, Y⋅Liu, L⋅Hua, Duy H⋅Kraft, Susan L⋅Basaraba, R J and Perchellet, J P
International journal of oncology, vol. 12, (no. 2), pp. 433-42, 1998/Feb. | Journal Article
1997
Anticancer activities of 2,5,8,9-substituted 6-oxo-1,2,3,4,5,6-hexahydrophenanthridines on multi-drug-resistant phenotype cells.
Hua, Duy H⋅Saha, S and Takemoto, Dolores J
Anticancer research, vol. 17, (no. 4A), pp. 2435-41, 1997 Jul-Aug. | Journal Article
 
Antitumor activity of novel tricyclic pyrone analogs in murine leukemia cells in vitro.
Perchellet, J P⋅Newell, S W⋅Ladesich, J B⋅Perchellet, E M⋅Chen, Y⋅Hua, Duy H⋅Kraft, Susan L⋅Basaraba, R J⋅Omura, S and Tomoda, H
Anticancer research, vol. 17, (no. 4A), pp. 2427-34, 1997 Jul-Aug. | Journal Article