Synthesis 2016; 48(14): 2245-2254
DOI: 10.1055/s-0035-1561598
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Novel 3,19-Dihydroxyjolkinolides and Related Derivatives Starting from Andrographolide

Ke Wang
a   Center of Drug Discovery, China Pharmaceutical University, 24 Tongjia Xiang Road, Nanjing 210009, P. R. of China
,
Yang-Chang Wu
b   School of Pharmacy, College of Pharmacy, China Medical University, 91 Hsueh-Shih Road, Taichung 40402, Taiwan, ROC
c   Chinese Medicine Research and Development Center, China Medical University Hospital, Taichung 40447, Taiwan, ROC
,
Juan-Cheng Yang
b   School of Pharmacy, College of Pharmacy, China Medical University, 91 Hsueh-Shih Road, Taichung 40402, Taiwan, ROC
c   Chinese Medicine Research and Development Center, China Medical University Hospital, Taichung 40447, Taiwan, ROC
,
Meng-Han Zhang
a   Center of Drug Discovery, China Pharmaceutical University, 24 Tongjia Xiang Road, Nanjing 210009, P. R. of China
,
Mohamed El-Shazly
d   Department of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, Ain Shams University, Organization of African Unity Street, Abassia, Cairo 11566, Egypt   Email: zhangdayong@cpu.edu.cn   Email: xmwu@cpu.edu.cn
,
Da-Yong Zhang*
a   Center of Drug Discovery, China Pharmaceutical University, 24 Tongjia Xiang Road, Nanjing 210009, P. R. of China
,
Xiao-Ming Wu*
a   Center of Drug Discovery, China Pharmaceutical University, 24 Tongjia Xiang Road, Nanjing 210009, P. R. of China
› Author Affiliations
Further Information

Publication History

Received: 20 January 2016

Accepted after revision: 07 March 2016

Publication Date:
03 May 2016 (online)


Abstract

The jolkinolides are a series of naturally occurring ent-abietane diterpenes with potent antitumor activity, which have been isolated from the genus Euphorbia. We describe the first method for the total synthesis of 3,19-dihydroxyjolkinolide and its derivatives. The strategy for the synthesis of 3,19-dihydroxyjolkinolide A has 12 steps with an overall yield of 4.3%. The synthesized compounds were evaluated for their antitumor activity in nine kinds of tumor cell lines.

Supporting Information

 
  • References

  • 1 Hanson JR. Nat. Prod. Rep. 2015; 32: 76
  • 2 Shi Q.-W, Su X.-H, Kiyota H. Chem. Rev. 2008; 108: 4295
  • 3 Wu Q.-C, Tang Y.-P, Ding A.-W, You F.-Q, Zhang L, Duan J.-A. Molecules 2009; 14: 4454
  • 4 Wang Y.-B, Huang R, Wang H.-B, Jin H.-Z, Lou L.-G, Qin G.-W. J. Nat. Prod. 2006; 69: 967
  • 5 Shi H.-M, Williams ID, Sung HH.-Y, Zhu H.-X, Ip NY, Min Z.-D. Planta Med. 2005; 71: 349
  • 6 Kalesse M, Christmann M, Bhatt U, Quitschalle M, Claus E, Saeed A, Burzlaff A, Kasper C, Haustedt LO, Hofer E, Scheper T, Beil W. ChemBioChem 2001; 2: 709
  • 7 Shi L.-Y, Wu J.-Q, Zhang D.-Y, Wu Y.-C, Hua W.-Y, Wu X.-M. Synthesis 2011; 3807
  • 8 Zhu C.-Z, Wang K, Zhang M.-H, Zhang D.-Y, Wu Y.-C, Wu X.-M, Hua W.-Y. Synthesis 2014; 46: 2574
  • 9 Valente C, Pedro M, Duarte A, Nascimento M, Abreu P, Ferreira M. J. Nat. Prod. 2004; 67: 902
  • 10 Yu L.-G, Ni T.-F, Gao W, He Y, Wang Y.-Y, Cui H.-W, Yang C.-G, Qiu W.-W. Eur. J. Med. Chem. 2015; 90: 10
  • 11 Lu Z.-Q, Guan S.-H, Li X.-N, Chen G.-T, Zhang J.-Q, Huang H.-L, Liu X, Guo D.-A. J. Nat. Prod. 2008; 71: 873
  • 12 Liu C, Liao Z.-X, Liu S.-J, Qu Y.-B, Wang H.-S. Fitoterapia 2014; 96: 33
  • 13 Lage H, Duarte N, Coburger C, Hilgeroth A, Ferreira MJ. U. Phytomedicine 2010; 17: 441
  • 14 Katsumura S, Kimura A, Isoe S. Tetrahedron 1989; 45: 1337
  • 15 Nanduri S, Nyavanandi VK, Thunuguntla SS, Kasu S, Pallerla MK, Ram PS, Rajagopal S, Kumar RA, Ramanujam R, Babu JM, Vyas K, Devi AS, Reddy GO, Akella V. Bioorg. Med. Chem. Lett. 2004; 14: 4711
  • 16 Crowe DF, Christie PH, DeGraw JI, Fujiwara AN, Grange E, Lim P, Tanabe M, Cairns T, Skelly G. Tetrahedron 1983; 39: 3083
  • 17 Bonjoch J, Cuesta J, Díaz S, González A. Tetrahedron Lett. 2000; 41: 5669
  • 18 Brasca MG, Amboldi N, Ballinari D, Cameron A, Casale E, Cervi G, Colombo M, Colotta F, Croci V, D’Alessio R, Fiorentini F, Isacchi A, Mercurio C, Moretti W, Panzeri A, Pastori W, Pevarello P, Quartieri F, Roletto F, Traquandi G, Vianello P, Vulpetti A, Ciomei M. J. Med. Chem. 2009; 52: 5152
  • 19 Wasserman HH, Ives JL. J. Org. Chem. 1985; 50: 3573
  • 20 Cytotoxicity assay in vitro: the human cancer cell lines were provided by Prof. Yang-Chang Wu’s group (China Medical University) and Prof. Qinglong Guo’s group (China Pharmaceutical University). The cell lines were maintained in a humidified atmosphere at 37 °C in 5% CO2. Cell cytotoxicity was determined by MTT assay. Cells were seeded in 96-well plates at a dosage of 5000 cells/well and incubated for 24 h. Then, the tested compounds at different concentrations (1.5625, 3.125, 6.25, 12.5, 25, 50, 100 μM) were added to the wells. After 48 h, the medium in each well was changed to MTT solution (0.5 mg/mL). After incubation for 1 h, the MTT solution was replaced by DMSO (100 μL) to dissolve the reduced MTT crystals. The absorbance of each well was measured at 570 nm by a microplate reader.