Publications

  1. Rajaputra, P., Bio, M., Thapa, P., You, Y.* Photo-unclick chemistry and its application to visible/near IR-activatable prodrugs for a combination of PDT and site-specific chemotherapy. Methods Mol. Biol. in press. - An Invited Book Chapter

  2. Subramaniyan, B., Rajaputra, P., Nguyen, L., Li, M., Peer, C. J., Kindrick, J., Figg, W. D., Woo, S., You, Y.* Local and Systemic Antitumor Effects of Photo-activatable Paclitaxel Prodrug on Rat Breast Tumor Models. Photochem. Photobiol. in press.
  1. Li, M., Nguyen, L., Subramaniyan, B., Bio, M., Peer, C. J., Kindrick, J., Figg, W. D., Woo, S.,* You, Y.* PBPK modeling-based optimization of site-specific chemo-photodynamic therapy with far-red light-activatable paclitaxel prodrug. J. Control. Release. 2019, 308, 86-97. [abstract]

  2. Bio, M., Rahman, M. K. M., Lim, I., Rajaputra, P., Hurst, R. E., You, Y.* Singlet oxygen-activatable Paclitaxel prodrugs via intermolecular activation for combined PDT and chemotherapy. Bioorg. Med. Chem. Lett. 2019, 29, 1537-1540. [abstract]
  3. https://www.sciencedirect.com/science/article/pii/S0960894X19302070?via%3Dihub

  4. Thapa, P., Li, M., Karki, R., Bio, M., Rajaputra, P., Nkepang, G., Woo, S., You, Y.* Folate-PEG conjugates of a far-red light-activatable paclitaxel prodrug to improve selectivity towards folate receptor-positive cancer cells. ACS Omega 2017, 2, 6349-6360. [abstract]

  5. Li, M., Thapa, P., Rajaputra, P., Bio, M., Peer, C. J., Figg, W. D., You, Y.,* Woo, S.* Quantitative modeling of the dynamics and intracellular trafficking of far-red light-activatable prodrugs: implications in stimuli-responsive drug delivery system. J. Pharmacokinet. Pharmacodyn. 2017, 44, 521-536. [abstract] Journal Cover Article
       

  6. Bio, M., Rajaputra, P., Lim, I., Thapa, P., Tienabeso, B., Hurst, R. E., You, Y.* Efficient activation of visible light-activatable CA4 prodrug through intermolecular photo-unclick chemistry in mitochondria. Chem. Comm. 2017, 53, 1884-1887. [abstract]
    1. http://pubs.rsc.org/en/content/articlepdf/2017/cc/c6cc09994g

  7. Thapa, P., Li, M., Bio, M., Rajaputra, P., Nkepang, G., Sun, Y., Woo, S., You, Y.* Far-red light-activatable prodrug of paclitaxel for the combined effects of photodynamic therapy and site-specific paclitaxel chemotherapy. J. Med. Chem.   2016, 59, 3204–3214. [abstract] Highlighted in ChemistryViews
  8. http://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.5b01971

  9. Rajaputra, P., Bio, M., Nkepang, G., Thapa, P., Woo, S., You, Y.* Anticancer drug released from near IR-activated prodrug overcomes spatiotemporal limits of singlet oxygen. Bioorg. Med. Chem. 2016, 24, 1540-1549. [abstract]
  10. http://www.sciencedirect.com/science/article/pii/S0968089616301134

  11. Bio, M., Rajaputra, P., You, Y.* Photodynamic therapy via FRET following bioorthogonal click reaction in cancer cells. Bioorg. Med. Chem. Lett. 2016, 26, 145-148. [abstract]

  12. Muli, D. K., Rajaputra, P., You, Y.,* McGrath, D. V.* Asymmetric ZnPc–TEG photosensitizers: the effect of Pc substitution on phototoxicity. Tetrahedron Lett. 2015, 56, 6236-6239. [abstract]
     
  13. Hurst, R. E.,* Hauser, P. J., You, Y., Bailey-Downs, L. C., Bastian, A., Mathews, S. M., Thorpe, J., Earle, C., Bourguignon L. Y. Y., Ihnat, M. I. Identification of novel drugs to target dormant micrometastases, BMC Cancer 2015, 15, 404. [abstract].

  14. Watley, R. L., Awuah, S. G., Bio, M., Cantu, R., Gobeze, H. H., Nesterov, V., N., D'Souza, F.* You, Y.* Dual functioning thieno-pyrrole fused BODIPY dyes for NIR optical imaging and photodynamic therapy – singlet oxygen generation without heavy halogen atom assistance, Chem. Asian J. 2015, 10, 1335-1343. [abstract]
  15. http://onlinelibrary.wiley.com/doi/10.1002/asia.201500140/abstract   http://onlinelibrary.wiley.com/doi/10.1002/asia.201580604/abstract

  16. Nkepang, G., Bio, M., Rajaputra, P., Awuah, S., You, Y.* Folate receptor-mediated enhanced and specific delivery of far-red light-activatable prodrugs of Combretastatin A-4 to FR-positive tumor, Bioconjugate Chem. 2014, 25, 2175-2188. [abstract]

  17. Muli, D. K.,  Rajaputra, R., You, Y.*, McGrath, D. V.* Asymmetric ZnPc-Rhodamine B conjugates for mitochondrial targeted photodynamic therapy, Bioorg. Med. Chem. Lett. 2014, 24, 4496-4500 [abstract]
  18. http://www.sciencedirect.com/science/article/pii/S0960894X14008178


  19. Bandi, V., Das, S., Awuah, S., You, Y.*, D'Souza, F.*, Thieno-Pyrrole-Fused BODIPY – Fullerene Dyads: Utilization of Near-Infrared Sensitizers for Ultrafast Charge Separation in Donor-Acceptor Systems, J. Am. Chem. Soc. 2014, 136, 7571-7574. [abstract
    http://pubs.acs.org/doi/abs/10.1021/ja503015f

  20. Bio, M., Rajaputra, P., Nkepang, G., You, Y.*, A far-red light activatable, multi-functional prodrug for fluorescence optical imaging and combinational treatment, J. Med. Chem. 2014, 57, 3401-3409. [abstract]
           
  1. Nkepang, G., You, Y. Heteroatom-substituted dioxetanes and their emerging biomedical applications. In Patai's Chemistry of Functional Groups, Edited by I. Marek. John Wiley & Sons, Ltd: Chichester, UK.  Published online 04/28/2014. [abstract] - An Invited Book Chapter

  2. Awuah, S. G.; Das, S.; D'Souza, F.; You, Y.* Thieno-pyrrole fused BODIPY intermediate as platform for multi-functional NIR agents, Chemistry - An Asian Journal 2013, 8, 3123-3132. [abstract]

  3. Bio, M., You, Y.*, Emerging strategies for controlling drug release by using visible/near IR light, Med. Chem. 2013, 3, 192-198. [abstract] - An Invited Review Article
  4. https://www.omicsonline.org/emerging-strategies-for-controlling-drug-release-by-using-visiblenear-ir-light-2161-0444.1000138.php?aid=14325

  5. Bio, M., Rajaputra, P., Nkepang, G., Awuah, S. G., Hossion, A. M. L., You, Y.*, Site-specific and far-red light-activatable prodrug of combretastain A-4 using photo-unclick chemistry, J. Med. Chem. 2013, 56, 3936-3942. [abstract] - Highlighted in SciBX: Science-Business eXchange

  6. Ngen, E., Xiao, L., Rajaputra, P., Yan, X.*, You, Y.*, Enhanced singlet oxygen generation from porphyrin-rhodamine B dyad by two-photon excitation through resonance energy transfer, Photochem. Photobiol. 2013, 89, 841-848 [abstract]
  1. Rajaputra, P., Nkepang, G., Watley, R., You, Y.*, Synthesis and in vitro biological evaluation of lipophilic cation conjugated photosensitizers for targeting mitochondria, Bioorg. Med. Chem. 2013, 21 (2), 379-387.
 [abstract]
  1. Hossion, A. M. L., Bio, M., Nkepang, G., Awuah, S. G., You, Y.*, Visible light controlled release of anti-cancer drug through double activation of prodrug, ACS Med. Chem. Lett. 2013, 4, 124-127. [abstract] - Highlighted in the Editor's Choice
  1. Awuah, G. S., You, Y.*, Boron dipyrromethene (BODIPY) based photosensitizers for photodynamic therapy. RSC Advances 2012, 2(30), 11169-11183. [abstract] - Review Article - Top ten most accessed articles in September
  1. Bio, M., Nkepang, G., You, Y.*, Click and photo-unclick chemistry of aminoacrylate for visible light-triggered drug release, Chem. Comm. 2012, 48, 6517-6519. [abstract]
  1. Nkepang, G., Pogular, P.K., Bio, M., You, You.*, Synthesis and singlet oxygen reactivity of 1,2-diaryloxyethenes and selected sulfur and nitrogen analogs, Photochem. Photobiol. 2012, 88, 753-759. [abstract]
  1. Awuah, S. G., Polreis, J., Prakash, J., Qiao, Q., You, Y.*, New pyran dyes for dye-sensitized solar cells, J. Photochem. Photobiol. A 2011, 224, 116-122. [abstract]
  1. Paul, B., Rajaputra, P., You, Y.*, In vitro and in vivo photodynamic activity of core-modified porphyrin IY69 using 690 nm diode laser, Photochem. Photobiol. 2011, 87, 1468-1473. [abstract]
  1. Awuah, S. G., Polreis, J., Biradar, V., You, Y.*, Singlet oxygen generation by novel NIR BODIPY dyes, Org. Lett. 2011, 13, 3884-3887. [abstract]
  1. Johnson, C., Darling, S. B., You, Y.*, Density functional theory as a guide for the design of pyran dyes for dye sensitized solar cells, Monatsh. Chem. 2011, 142, 45-52.[abstract]
  1. Ngen, E. J., Rajaputra, P., You, Y.*, Evaluation of delocalized lipophilic cationic dyes as delivery vehicles for photosensitizers to mitochondria, Bioorg. Med. Chem. 2009, 17, 6631-6640.[abstract]
  1. Murthy, R. M., Bio, M., You, Y.*, Low energy light-triggered oxidative cleavage of olefins, Tetrahedron Lett. 2009, 50, 1041-1044[abstract]
  1. Xie, Y., Joshi, P., Ropp, M., Galipeau, D, Zhang, L., Fong, H., You, Y.*, Qiao, Q.*, Structural effects of core-modified porphyrins in dye-sensitized solar cells, J. Porphyrins Phthalocyanines 2009, 13, 903-909. [abstract]
  1. Minnes, M, Weitman, H., You, Y., Detty, M.R., Ehrenberg, B., Dithiaporphyrin derivatives as photosensitizers in membranes and cells. J. Phy. Chem. B 2008, 112, 3268-3276. [abstract]
  1. Ngen, E. J., Daniels, T. S., Murthy, R. S., Detty, M. R., You, Y.*, Core-modified porphyrins. Part 6: Effects of lipophilicity and core system on physicochemical and biological properties in vitro. Bioorg. Med. Chem. 2008, 16, 3171-3183[abstract]
  1. Chintharlapalli, S., Papineni, S., Liu, S., Jutooru, I., Chadalapaka, G., Cho, S., Murthy, R., You, Y., Safe, S., 2-Cyano-lup-1-en-3-oxo-20-oic acid, a cyano derivative of betulinic acid activates peroxisome proliferator-activated receptor g in colon and pancreatic cancer cells. Carcinogenesis 2007, 28, 2337-2346.  [abstract]
  1. You, Y.*, Daniels, T. S., Dominiak, P. M., Detty, M. R., Synthesis, spectral data, and crystal structure of two novel substitution patterns in dithiaporphyrins. J. Porphyrins Phthalocyanines 2007, 11, 1-8. [abstract]
  1. You, Y.*, Gibson, S. L., Detty, M. R., Phototoxicity of a core-modified porphyrin and induction of apoptosis. J. Photochem. Photobiol., B. 2006, 85, 155-162. [abstract]
  1. Tombline, G., Donnelly, D. J., Holt, J. J., You, Y., Ye, M., Gannon, M. K., Nygren, C. L., Detty, M. R., Stimulation of P-glycoprotein ATPase by analogues of tetramethylrosamine: coupling of drug binding at the "R" site to the ATP hydrolysis transition state. Biochemistry 2006, 45, 8037-8047. [abstract]
  1. Gibson, S. L., Holt, J. J., Ye, M., Donnelly, D. J., Ohulchanskyy, T. Y., You, Y., Detty, M. R., Structure-activity studies of uptake and phototoxicity with heavy-chalcogen analogues of tetramethylrosamine in vitro in chemosensitive and multidrug-resistant cells. Bioorg. Med. Chem. 2005, 13, 6394-6403. [abstract]
  1. You, Y.*, Gibson, S. L., Detty, M. R., Core-modified porphyrins. Part 5: electronic effects on photophysical and biological properties in vitro. Bioorg. Med. Chem. 2005, 13, 5968-5980. [abstract]
  1. You, Y.*, Gibson, S.L., Hilf, R., Ohulchanskyy, T.Y., Detty, M.R.,* Core-modified porphyrins. Part 4: steric effects on photophysical and biological properties in vitro. Bioorg. Med. Chem. 2005, 13, 2235-2261. [abstract]   
  1. You, Y.*, Podophyllotoxin Derivatives: Current synthetic approaches for new anticancer agents. Curr. Pharm. Design 200511, 1695-1717. (invited review) [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., New constituents from Crinum latifolium with inhibitory effects against tube-like formation of human umbilical venous endothelial cells. Nat. Prod. Res. 2004, 18, 485-491. [abstract]
  1. Nam, N. H., Hong, D. H., You, Y. J., Kim, Y., Bang, S. C., Kim, H. M., Ahn, B. Z., Synthesis and cytotoxicity of 2,5-dihydroxychalcones and related compounds. Arch. Pharm. Res. 2004, 27, 581-588. [abstract]
  1. You, Y., Kim, Y., Nam, N.H., Bang, S. C., Ahn, B.Z., Alkyl and carboxyalkyl esters of 4'-demethyl-4-deoxypodophyllotoxin: synthesis, cytotoxic, and antitumor activity. Europ. J. Med. Chem. 2004, 39, 189-193. [abstract]
  1. You, Y., Kim, Y., Nam, N.H., Ahn, B.Z., Lupane derivatives: synthesis and cytotoxic activity-III, A-ring modified derivatives. Bioorg. Med. Chem. Lett. 200313, 3137-3140. [abstract]
  1. You, Y., Gibson, S.L., Hilf, R., Davies, S.R., Oserff, A.R., Roy, I., Ohulchansky, T.Y., Bergey, E.J., Detty, M.R., Water-soluble, core-modified porphyrins. III. synthesis, photophysical properties, and in Vitro studies of cellular uptake, distribution and photosensitization with carboxilic acid substituted derivatives. J. Med. Chem. 2003, 46, 3734-3747. [abstract]
  1. You, Y., Kim, Y., Nam, N.H., Ahn, B.Z., Antitumor activity of unsaturated fatty acid esters of 4’-demethyldeoxypodophyllotoxin. Bioorg. Med. Chem. Lett. 2003, 13, 2629-2632. [abstract]
  1. Ahsan, K., Drake, M. D., Higgs, D. E., Wojciechowski, A. L., Tse, B. N., Beteman, M. A., You, Y., Detty, M. R., Dendrimeric organotelluride catalysts for the activation of hydrogen peroxide. Improved catalytic activity through statistical and stereoelectronic effects. Organometallics 2003, 22, 2883-2890. [abstract]
  1. You, Y., Kim, Y., Nam, N.H., Ahn, B.Z., Inhibitory effect of Adonis amurensis components on tube-like formation of human umbilical venous cells. Phytother. Res. 2003, 17, 568-570. [abstract]
  1. You, Y., Ahsan, K., Detty, M.R., Mechanistic studies of the tellurium(II)/tellurium(IV) redox cycle in thiol peroxidase-like reactions of diorganotellurides in methanol. J. Am. Chem. Soc. 2003, 125, 4918-4927. [abstract]
  1. You, Y., Nam, N.H., Kim, Y., Bae, K.H., Ahn, B.Z., Antiangiogenic activity of lupeol from Bombax ceiba. Phytother. Res. 2003, 17, 341-344. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Water soluble prodrugs of the antitumor agent 3-[(3-amino-4-methoxy)phenyl]-2-(3,4,5-trimethoxyphenyl)cyclopent-2-ene-1- one. Bioorg. Med. Chem. 2003, 11, 1021-1029. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Cytotoxic 2',5'-dihydroxychalcones with unexpected antiangiogenic activity. Eur. J. Med. Chem. 2003, 38, 179-187. [abstract]
  1. You, Y., Kim, Y., Nam, N.H., Ahn, B.Z., Synthesis and cytotoxic activity-II, aminoacetyl derivatives. Yakhak Hoeji 2002, 46, 301-306. [abstract]
  1. You, Y., Kim, Y., Ahn, B.Z., Lupane derivatives-I: synthesis and cytotoxic activity. Yakhak Hoeji 2002, 46, 295-300. [abstract]
  1. Cuong, N.-M., Nam, N.-H., Kim, Y., You, Y.-J., Bae, K.-H., Sung, T.-V., Ahn, B.-Z., Cytotoxic activity of Vietnamese herbal medicines against A549 cells. Kor. J. Pharmacogn. 2002, 33, 64-68. [abstract]
  1. Kim, Y., You, Y., Nam, N. H., Ahn, B. Z., Prodrugs of 4'-demethyl-4-deoxypodophyllotoxin: synthesis and evaluation of the antitumor activity. Bioorg. Med. Chem. Lett. 200212(23), 3435-3438. [abstract]
  1. Abe, M., You, Y., Detty, M. R., 21-Telluraporphyrins. II. Catalysts for bromination reactions with hydrogen peroxide and sodium bromide. Organometallics 2002, 21, 4546-4551. [abstract]
  1. You, Y., Lee, I.S., Kim, Y., Bae, K.H., Ahn, B.Z., Antiangiogenic activity of Bupleurum longiradiatum on human umbilical venous endothelial cells. Arch. Pharm. Res. 2002, 25(5), 640-642. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Synthesis, cytotoxicity and antitumor activity of 2,3-diarylcyclopent-2-ene-1-ones. Arch. Pharm. Res. 2002, 25, 600-607. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Synthesis and anti-tumor activity of novel combretastatins: combretocyclopentenones and related analogues. Bioorg. Med. Chem. Lett. 2002, 12, 1955-1958. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Preliminary structure-antiangiogenic activity relationships of 4-senecioyloxymethyl-6,7-dimethoxycoumarin. Bioorg. Med. Chem. Lett. 2002, 12, 2345-2348. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Synthesis and cytotoxicity of some rigid derivatives of methyl 2,5-dihydroxycinnamate. Arch. Pharm. Res. 2002, 25, 590-599. [abstract]
  1. Kim, Y., You, Y., Nam, N. H., Ahn, B. Z., 2,3-Dibenzylbutyrolactones and 1,2,3,4-tetrahydro-2-naphthoic acid gamma-lactones: structure and activity relationship in cytotoxic activity. Arch. Pharm. Res. 2002, 25, 240-249. [abstract]
  1. Kim, Y., You, Y., Kim, S. B., Ahn, B. Z., Deoxypodophyllotoxin; the cytotoxic and antiangiogenic component from Pulsatilla koreana Nakai. Planta Med. 2002, 68, 271-274. [abstract]
  1. Kim, Y., Nam, N. H., You, Y. J., Ahn, B. Z., Synthesis and cytotoxicity of 3,4-diaryl-2(5H)-furanones. Bioorg. Med. Chem. Lett. 2002, 12, 719-722. [abstract]
  1. Nam, N. H., Kim, Y., You, Y. J., Hong, D. H., Kim, H. M., Ahn, B. Z., Combretoxazolones: synthesis, cytotoxicity and antitumor activity. Bioorg. Med. Chem. Lett. 2001, 11, 3073-3076. [abstract]
  1. Kim, Y., You, Y. J., Ahn, B. Z., 6-(1-Acyloxyalkyl)-5,8-Dimethoxy-1,4-Naphthoquinones: Synthesis and evaluation of inhibitory effect on DNA topoisomerase-I and cytotoxic activity. Arch. Pharm. (Weinheim) 2001, 334, 318-322. [abstract]
  1. Jin, G. J., You, Y. J., Ahn, B .Z., Esters of 2-(1-hydroxy- alkyl)-1,4-dihydroxy-9,10-anthraquinones with melphalan as multifunctional anticancer agents. Bioorg. Med. Chem. Lett. 2001, 11, 1473-1476. [abstract]
  1. Shin, D. J., You, Y. J., Ahn, B. Z., 2-(1-Aminoacetylalkyl)-1,4-dihydroxy-9,10-antraquinones derivatives: synthesis and cytotoxic activity. Yakhak Hoeji 2001, 45, 133-139. [abstract]
  1. Nam, N. H., You, Y. J., Kim, Y., Hong, D. H., Kim, H. M., Ahn, B. Z., Synthesis of certain 3-aryl-2-propenoates and evaluation of their cytotoxicity. Bioorg. Med. Chem. Lett. 2001, 11, 1173-1176. [abstract]
  1. Jin, G.J., You, Y. J., Kim, Y., Nam, N. H., Ahn, B. Z., Esters of chlorambucil with 2-substituted 1,4-dihydroxy-9,10-anthraquinones as multifunctional anticancer agents. Europ. J. Med. Chem. 2001, 36, 361-366. [abstract]
  1. Song, G. Y., Kim, Y., You, Y. J., Cho, H., Ahn, B. Z., Naphthazarin derivatives (VII): antitumor action against ICR mice bearing ascitic S-180 cells. Arch. Pharm. Res. 2001, 24, 35-38. [abstract]
  1. You, Y., Kim, Y., Song, G. Y., Ahn, B. Z., (E)-6-(1-Alkyloxyiminoalkyl)-5,8-dimethoxy-1,4-naphthoquinones: synthesis, cytotoxic activity and antitumor activity. Bioorg. Med. Chem. Lett. 2000, 10, 2301-2303. [abstract]
  1. Bae, K. H., You, Y. J., Park, J. Y., An, R. B., Kim, Y. H., Kang, J. S., Ahn, B. Z., Screening of angiogenesis inhibitors from Korean plants (I). Kor. J. Pharmacogn. 2000, 31(3), 320-324. [abstract]
  1. Song, G. Y., Kim, Y., You, Y. J., Cho, H., Kim, S. H., Sok, D. E., Ahn, B. Z., Naphthazarin derivatives (VI): synthesis, inhibitory effect on DNA topoisomerase-I and antiproliferative activity of 2- or 6-(1-oxyiminoalkyl)-5,8-dimethoxy-1,4-naphthoquinones. Arch. Pharm. (Weinheim) 2000, 333, 87-92. [abstract] 
  1. Song, G. Y., Kim, Y., Zheng, X. G., You, Y. J., Cho, H., Chung, J. H., Sok, D. E., Ahn, B. Z., Naphthazarin derivatives (IV): synthesis, inhibition of DNA topoisomerase I and cytotoxicity of 2- or 6-acyl-5,8-dimethoxy-1, 4-naphthoquinones. Eur. J. Med. Chem. 2000, 35, 291-298. [abstract]
  1. Do, Q. V., Pharm, G. D., Mai, N. T., Nguyen, H. N., You, Y. J., Ahn, B. Z., Cytotoxicity of some anthraquinones from the stem of Morinda citrifolia growing in Vietnam. Tap chi Hoa hoc (Vietnamese J. of Chemistry) 1999, 37, 94-97.
  1. Song, G. Y., Zheng, X. G., Kim, Y., You, Y. J., Sok, D. E., Ahn, B. Z., Naphthazarin derivatives (II): formation of glutathione conjugate, inhibition of DNA topoisomerase-I and cytotoxicity. Bioorg. Med. Chem. Lett. 1999, 9, 2407-2412. [abstract]
  1. Zheng, X. G., Kang, J. S., Kim, Y., You, Y. J., Jin, G. Z., Ahn, B. Z., Glutathione conjugates of 2- or 6-substituted 5,8-dimethoxy-1,4-naphthoquinone derivatives: formation and structure. Arch. Pharm. Res. 1999, 22, 384-390. [abstract]
  1. You, Y. J., Ahn, B. Z., 6-(1-Alkenoyloxyalkyl)-5,8-dimethoxynaphthoquinone derivatives: synthesis and evaluation of antitumor activity. Arch. Pharm. Res. 1998, 21(6), 738-743. [abstract]
  1. You, Y. J., Zheng, X. G., Kim, Y., Ahn, B. Z., Naphthazarin derivatives: synthesis, formation of glutahtione conjugate, inhibition of DNA topoisomerase-I and antitumor activity. Arch. Pharm. Res. 1998, 21, 595-598. [abstract]