-
1
-
-
0001635377
-
Podophyllotoxin derivatives: Drug discovery and development
-
Bohlin, L.; Rosen, B. Podophyllotoxin derivatives: Drug discovery and development. Drug Discov.Today, 1996, 1, 343-51.
-
(1996)
Drug Discov.Today
, vol.1
, pp. 343-351
-
-
Bohlin, L.1
Rosen, B.2
-
2
-
-
0020035646
-
The podophyllotoxin derivatives VP16-213 and VM26
-
Issell, B.F. The podophyllotoxin derivatives VP16-213 and VM26. Cancer Chemother. Pharmacol., 1982, 7, 73-80.
-
(1982)
Cancer Chemother. Pharmacol
, vol.7
, pp. 73-80
-
-
Issell, B.F.1
-
3
-
-
0029856304
-
Etoposide phosphate, the water soluble prodrug of etoposide
-
Beijnen, J.H.; Witterland, A.H.; Koks, C.H.W. Etoposide phosphate, the water soluble prodrug of etoposide. Pharm.World Sci., 1996, 18, 163-70.
-
(1996)
Pharm.World Sci
, vol.18
, pp. 163-170
-
-
Beijnen, J.H.1
Witterland, A.H.2
Koks, C.H.W.3
-
4
-
-
0030464546
-
Early studies of etoposide phosphate, a watersoluble prodrug
-
Budman, D.R. Early studies of etoposide phosphate, a watersoluble prodrug. Semin. Oncol., 1996, 23, 8-14.
-
(1996)
Semin. Oncol
, vol.23
, pp. 8-14
-
-
Budman, D.R.1
-
5
-
-
0030468414
-
Clinical studies with etoposide phosphate
-
Greco, F.A.; Hainsworth, J.D. Clinical studies with etoposide phosphate. Semin. Oncol., 1996, 23, 45-50.
-
(1996)
Semin. Oncol
, vol.23
, pp. 45-50
-
-
Greco, F.A.1
Hainsworth, J.D.2
-
6
-
-
4043121827
-
Podophyllotoxin: Distribution, sources, applications and new cytotoxic derivatives
-
Gordaliza, M.; Garcia, P.A.; Miguel Del Corral, J.M.; Castro, M.A.; Gomez-Zurita, M.A. Podophyllotoxin: distribution, sources, applications and new cytotoxic derivatives. Toxicon, 2004, 44, 441-59.
-
(2004)
Toxicon
, vol.44
, pp. 441-459
-
-
Gordaliza, M.1
Garcia, P.A.2
Miguel, D.C.J.M.3
Castro, M.A.4
Gomez-Zurita, M.A.5
-
7
-
-
18744373344
-
Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents
-
You, Y.J. Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents. Curr. Pharm. Des., 2005, 11, 1695-717.
-
(2005)
Curr. Pharm. Des
, vol.11
, pp. 1695-1717
-
-
You, Y.J.1
-
8
-
-
61949442809
-
A review on hemisynthesis, biosynthesis, biological activities, mode of action, and structure-activity relationship of podophyllotoxins: 2003-2007
-
Xu, H.; Lv, M.; Tian, X. A review on hemisynthesis, biosynthesis, biological activities, mode of action, and structure-activity relationship of podophyllotoxins: 2003-2007. Curr. Med. Chem., 2009, 16, 327-49.
-
(2009)
Curr. Med. Chem
, vol.16
, pp. 327-349
-
-
Xu, H.1
Lv, M.2
Tian, X.3
-
9
-
-
74349103565
-
Novel semisynthetic spin-labeled derivatives of podophyllotoxin with cytotoxic and antioxidative activity
-
Zhang, J.Q.; Zhang, Z.W.; Hui, L.; Chen, S.W.; Tian, X. Novel semisynthetic spin-labeled derivatives of podophyllotoxin with cytotoxic and antioxidative activity. Bioorg. Med. Chem. Lett., 2010, 20, 983-6.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 983-986
-
-
Zhang, J.Q.1
Zhang, Z.W.2
Hui, L.3
Chen, S.W.4
Tian, X.5
-
10
-
-
76649095637
-
Podophyllotoxin analogues active versus Trypanosoma brucei
-
Uddin, M.J.; Smithson, D.C.; Brown, K.M.; Crews, B.C.; Connelly, M.; Zhu, F.Y.; Marnett, L.J.; Guy, R.K. Podophyllotoxin analogues active versus Trypanosoma brucei. Bioorg. Med. Chem. Lett., 2010, 20, 1787-91.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 1787-1791
-
-
Uddin, M.J.1
Smithson, D.C.2
Brown, K.M.3
Crews, B.C.4
Connelly, M.5
Zhu, F.Y.6
Marnett, L.J.7
Guy, R.K.8
-
11
-
-
77953537458
-
Podophyllotoxin induces CREB phosphorylation and CRE-driven gene expression via PKA but not MAPKs
-
Chen, Y.Q.; Xie, X. Podophyllotoxin induces CREB phosphorylation and CRE-driven gene expression via PKA but not MAPKs. Mol. Cell., 2010, 29, 41-50.
-
(2010)
Mol. Cell
, vol.29
, pp. 41-50
-
-
Chen, Y.Q.1
Xie, X.2
-
12
-
-
69949191350
-
Semisynthesis and quantitative structure-activity relationship (QSAR) study of novel aromatic esters of 4'-demethyl-4- deoxypodophyllotoxin as insecticidal agents
-
Xu, H.; Wang, J.J.; Sun, H.J.; Lv, M.; Tian, X.; Yao, X.J.; Zhang, X. Semisynthesis and quantitative structure-activity relationship (QSAR) study of novel aromatic esters of 4'-demethyl-4- deoxypodophyllotoxin as insecticidal agents. J. Agric. Food Chem., 2009, 57, 7919-23.
-
(2009)
J. Agric. Food Chem
, vol.57
, pp. 7919-7923
-
-
Xu, H.1
Wang, J.J.2
Sun, H.J.3
Lv, M.4
Tian, X.5
Yao, X.J.6
Zhang, X.7
-
13
-
-
68949180383
-
Natural products-based insecticidal agents 4. Semisynthesis and insecticidal activity of novel esters of 2-chloropodophyllotoxin against Mythimna separata Walker in vivo
-
Xu, H.; Xiao, X. Natural products-based insecticidal agents 4. Semisynthesis and insecticidal activity of novel esters of 2-chloropodophyllotoxin against Mythimna separata Walker in vivo. Bioorg. Med. Chem. Lett., 2009, 19, 5415-8.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 5415-5418
-
-
Xu, H.1
Xiao, X.2
-
14
-
-
77950098745
-
Natural products-based insecticidal agents 5. Design, semisynthesis and insecticidal activity of novel 4'-substituted benzenesulfonate derivatives of 4-deoxypodophyllotoxin against Mythimna separata Walker in vivo
-
Xu, H.; Wang, J.J. Natural products-based insecticidal agents 5. Design, semisynthesis and insecticidal activity of novel 4'-substituted benzenesulfonate derivatives of 4-deoxypodophyllotoxin against Mythimna separata Walker in vivo. Bioorg. Med. Chem. Lett., 2010, 20, 2500-2.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 2500-2502
-
-
Xu, H.1
Wang, J.J.2
-
15
-
-
77955414114
-
Natural products-based insecticidal agents 6. Design, semisynthesis and insecticidal activity of novel monomethyl phthalate derivatives of podophyllotoxin against Mythimna separata Walker in vivo
-
Xu, H.; He, X.Q. Natural products-based insecticidal agents 6. Design, semisynthesis and insecticidal activity of novel monomethyl phthalate derivatives of podophyllotoxin against Mythimna separata Walker in vivo. Bioorg. Med. Chem. Lett., 2010, 20, 4503-6.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 4503-4506
-
-
Xu, H.1
He, X.Q.2
-
16
-
-
77955657330
-
Natural products-based insecticidal agents 7. Semisynthesis and insecticidal activity of novel 4α-alkyloxy-2-chloropodophyllotoxin derivatives against Mythimna separata Walker in vivo
-
Xu, H.; Xiao, X.; Wang, Q.T. Natural products-based insecticidal agents 7. Semisynthesis and insecticidal activity of novel 4α-alkyloxy-2-chloropodophyllotoxin derivatives against Mythimna separata Walker in vivo. Bioorg. Med. Chem. Lett., 2010, 20, 5009-12.
-
(2010)
Biorg. Med. Chem. Lett
, vol.20
, pp. 5009-5012
-
-
Xu, H.1
Xiao, X.2
Wang, Q.T.3
-
17
-
-
77956711171
-
Podophyllotoxin derivatives show activity against Brontispa longissima larvae
-
Zhang, J.; Liu, Y.Q.; Yang, L.; Feng, G. Podophyllotoxin derivatives show activity against Brontispa longissima larvae. Nat. Prod. Commun., 2010, 5, 1247-50.
-
(2010)
Nat. Prod. Commun
, vol.5
, pp. 1247-1250
-
-
Zhang, J.1
Liu, Y.Q.2
Yang, L.3
Feng, G.4
-
18
-
-
78650910563
-
Evaluation of insecticidal activity of podophyllotoxin derivatives against Brontispa longissima
-
Liu, Y.Q.; Zhao, C.Y.; Yang, L.; Zhao, Y.L.; Liu, T.T. Evaluation of insecticidal activity of podophyllotoxin derivatives against Brontispa longissima. Pestic. Biochem. Physiol., 2011, 99, 39-44.
-
(2011)
Pestic. Biochem. Physiol
, vol.99
, pp. 39-44
-
-
Liu, Y.Q.1
Zhao, C.Y.2
Yang, L.3
Zhao, Y.L.4
Liu, T.T.5
-
19
-
-
33646856607
-
Oxalone and lactone moieties of podophyllotoxin exhibit properties of both the B and C Rings of colchicine in its binding with tubulin
-
Gupta, S.; Das, L.; Datta, A.B.; Poddar, A.; Janik, M.E.; Bhattacharyya, B. Oxalone and lactone moieties of podophyllotoxin exhibit properties of both the B and C Rings of colchicine in its binding with tubulin. Biochemistry, 2006, 45, 6467-75.
-
(2006)
Biochemistry
, vol.45
, pp. 6467-6475
-
-
Gupta, S.1
Das, L.2
Datta, A.B.3
Poddar, A.4
Janik, M.E.5
Bhattacharyya, B.6
-
20
-
-
0036086919
-
Drugs that inhibit tubulin polymerization: The particular case of podophyllotoxin and analogues
-
Desbene, S.; Giorgi-Renault, S. Drugs that inhibit tubulin polymerization: The particular case of podophyllotoxin and analogues. Curr. Med. Chem.- Anti-Cancer Agents, 2002, 2, 71-90.
-
(2002)
Curr. Med. Chem.-Anti-Cancer Agents
, vol.2
, pp. 71-90
-
-
Desbene, S.1
Giorgi-Renault, S.2
-
21
-
-
0024233051
-
Mechanism of action of antitumor drug etoposide: A review
-
Van Maanen, J.M.S.; Retel, J.; de Vries, J.; Pinedo, H.M. Mechanism of action of antitumor drug etoposide: A review. J. Natl. Cancer Inst., 1988, 80, 1526-33.
-
(1988)
J. Natl. Cancer Inst
, vol.80
, pp. 1526-1533
-
-
van Maanen, J.M.S.1
Retel, J.2
de Vries, J.3
Pinedo, H.M.4
-
22
-
-
0017030794
-
Effects of podophyllotoxin and VP-16- 213 on microtubule assembly in vitro and nucleoside transport in HeLa cells
-
Loike, J.D.; Horwitz, S.B. Effects of podophyllotoxin and VP-16- 213 on microtubule assembly in vitro and nucleoside transport in HeLa cells. Biochemistry, 1976, 15, 5435-43.
-
(1976)
Biochemistry
, vol.15
, pp. 5435-5443
-
-
Loike, J.D.1
Horwitz, S.B.2
-
23
-
-
43749114947
-
Podophyllotoxin directly binds a hinge domain in E2 of HPV and inhibits an E2/E7 interaction in vitro
-
Saitoh, T.; Kuramochi, K.; Imai, T.; Takata, K.; Takehara, M.; Kobayashi, S.; Sakaguchia, K.; Sugawaraa, F. Podophyllotoxin directly binds a hinge domain in E2 of HPV and inhibits an E2/E7 interaction in vitro. Bioorg. Med. Chem., 2008, 16, 5815-25.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 5815-5825
-
-
Saitoh, T.1
Kuramochi, K.2
Imai, T.3
Takata, K.4
Takehara, M.5
Kobayashi, S.6
Sakaguchia, K.7
Sugawaraa, F.8
-
24
-
-
67349128587
-
Deoxypodophyllotoxin, flavolignan, from Anthriscus sylvestris Hoffm. inhibits migration and MMP-9 via MAPK pathways in TNF-α-induced HASMC
-
Suh, S.-J.; Kim, J.-R.; Jin, U.-H.; Choi, H.-S.; Chang,Y.-C.; Lee, Y.-C.; Kim, S.-H.; Lee, I.-S.; Moon, T. C.; Chang, H.-W.; Kim, C.-H. Deoxypodophyllotoxin, flavolignan, from Anthriscus sylvestris Hoffm. inhibits migration and MMP-9 via MAPK pathways in TNF-α-induced HASMC. Vascular Pharmacol., 2009, 51, 13-20.
-
(2009)
Ascular Pharmacol
, vol.51
, pp. 13-20
-
-
Suh, S.-J.1
Kim, J.-R.2
Jin, U.-H.3
Choi, H.-S.4
Chang, Y.-C.5
Lee, Y.-C.6
Kim, S.-H.7
Lee, I.-S.8
Moon, T.C.9
Chang, H.-W.10
Kim, C.-H.11
-
25
-
-
67650162734
-
Antitumor activity of deoxypodophyllotoxin isolated from Anthriscus sylvestris: Induction of G2/M cell cycle arrest and caspase-dependent apoptosis
-
Yong, Y.; Shin, S.Y.; Lee, Y.H.; Lim, Y. Antitumor activity of deoxypodophyllotoxin isolated from Anthriscus sylvestris: Induction of G2/M cell cycle arrest and caspase-dependent apoptosis. Bioorg. Med. Chem. Lett., 2009, 19, 4367-71.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 4367-4371
-
-
Yong, Y.1
Shin, S.Y.2
Lee, Y.H.3
Lim, Y.4
-
26
-
-
72949083280
-
Deoxypodophyllotoxin induces G2/M cell cycle arrest and apoptosis in HeLa cells
-
Shin, S.Y.; Yong, Y.; Kim, C.G.; Lee, Y.H.; Lim, Y. Deoxypodophyllotoxin induces G2/M cell cycle arrest and apoptosis in HeLa cells. Cancer Lett., 2010, 287, 231-9.
-
(2010)
Cancer Lett
, vol.287
, pp. 231-239
-
-
Shin, S.Y.1
Yong, Y.2
Kim, C.G.3
Lee, Y.H.4
Lim, Y.5
-
27
-
-
0141516298
-
Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: A route to the podophyllotoxin skeleton
-
Clayden, J.; Kenworthy, M.N.; Helliwell, M. Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: A route to the podophyllotoxin skeleton. Org. Lett., 2003, 5, 831-4.
-
(2003)
Org. Lett
, vol.5
, pp. 831-834
-
-
Clayden, J.1
Kenworthy, M.N.2
Helliwell, M.3
-
28
-
-
0023768503
-
Asymmetric total synthesis of (-)-podophyllotoxin
-
Andrews, R.C.; Teague, S.J.; Meyers, A.I. Asymmetric total synthesis of (-)-podophyllotoxin. J. Am. Chem. Soc., 1988, 110, 7854-8.
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 7854-7858
-
-
Andrews, R.C.1
Teague, S.J.2
Meyers, A.I.3
-
29
-
-
0025755543
-
Enantioselective total synthesis of (-)-epipodophyllotoxin and (-)-podophyllotoxin
-
Van Speybroeck, R.; Guo, H.; Van der Eycken, J. Enantioselective total synthesis of (-)-epipodophyllotoxin and (-)-podophyllotoxin. Tetrahedron, 1991, 47, 4675-82.
-
(1991)
Tetrahedron
, vol.47
, pp. 4675-4682
-
-
van Speybroeck, R.1
Guo, H.2
van der, E.J.3
-
30
-
-
0026540546
-
Asymmetric synthesis of (-)- neopodophyllotoxin
-
Charlton, J.L.; Koh, K. Asymmetric synthesis of (-)- neopodophyllotoxin. J. Org. Chem., 1992, 57, 1514-6.
-
(1992)
J. Org. Chem
, vol.57
, pp. 1514-1516
-
-
Charlton, J.L.1
Koh, K.2
-
31
-
-
0141888982
-
The intramolecular carboxyarylation approach to podophyllotoxin
-
Reynolds, A.J.; Scott, A.J.; Turner, C.I.; Sherburn, M.S. The intramolecular carboxyarylation approach to podophyllotoxin. J. Am. Chem. Soc., 2003, 125, 12108-9.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 12108-12109
-
-
Reynolds, A.J.1
Scott, A.J.2
Turner, C.I.3
Sherburn, M.S.4
-
32
-
-
1242317875
-
Synthesis of advanced intermediates for the preparation of aza-analogues of podophyllotoxin
-
Marcantoni, E.; Petrini, M.; Profeta, R. Synthesis of advanced intermediates for the preparation of aza-analogues of podophyllotoxin. Tetrahedron Lett., 2004, 45, 2133-6.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 2133-2136
-
-
Marcantoni, E.1
Petrini, M.2
Profeta, R.3
-
33
-
-
44749094980
-
Isolation and identification of an endophytic strain of Fusarium oxysporum producing podophyllotoxin from Juniperus recurva
-
Kour, A.; Shawl, A.S.; Rehman, S.; Sultan, P.; Qazi, P.H.; Suden, P.; Khajuria, R.K.; Verma, V. Isolation and identification of an endophytic strain of Fusarium oxysporum producing podophyllotoxin from Juniperus recurva. World J. Microbiol. Biotechnol., 2008, 24, 1115-21.
-
(2008)
World J. Microbiol. Biotechnol
, vol.24
, pp. 1115-1121
-
-
Kour, A.1
Shawl, A.S.2
Rehman, S.3
Sultan, P.4
Qazi, P.H.5
Suden, P.6
Khajuria, R.K.7
Verma, V.8
-
34
-
-
60049095089
-
Podophyllotoxin production via cell and adventitious root cultures of Podophyllum peltatum
-
Anbazhagan, V.R.; Ahn, C.H.; Harada, E.; Kim, Y.S.; Choi, Y.E. Podophyllotoxin production via cell and adventitious root cultures of Podophyllum peltatum. In Vitro Cell. Dev. Biol.-Plant, 2008, 44, 494-501.
-
(2008)
In Vitro Cell. Dev. Biol.-Plant
, vol.44
, pp. 494-501
-
-
Anbazhagan, V.R.1
Ahn, C.H.2
Harada, E.3
Kim, Y.S.4
Choi, Y.E.5
-
35
-
-
68849116722
-
Aspergillus fumigatus Fresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drug deoxypodophyllotoxin
-
Kusari, S.; Lamshoft, M.; Spiteller, M. Aspergillus fumigatus Fresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drug deoxypodophyllotoxin. J. Appl. Microbiol., 2009, 107, 1019-30.
-
(2009)
J. Appl. Microbiol
, vol.107
, pp. 1019-1030
-
-
Kusari, S.1
Lamshoft, M.2
Spiteller, M.3
-
36
-
-
68349139463
-
Novel biotransformation process of podophyllotoxin to produce podophyllic acid and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066
-
Tang, Y.; Li, Y.; Zhong, J. Novel biotransformation process of podophyllotoxin to produce podophyllic acid and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066. Part I: Process development. Bioprocess Biosyst. Eng., 2009, 32, 663-71.
-
(2009)
Part I: Process development. Bioprocess Biosyst. Eng
, vol.32
, pp. 663-671
-
-
Tang, Y.1
Li, Y.2
Zhong, J.3
-
37
-
-
45749149086
-
Design, synthesis and cytotoxicity of novel podophyllotoxin derivatives
-
Yu, P.F.; Chen, H.; Wang, J.; He, C.X.; Cao, B.; Li, M.; Yang, N.; Lei, Z.Y.; Cheng, M.S. Design, synthesis and cytotoxicity of novel podophyllotoxin derivatives. Chem. Pharm. Bull., 2008, 56, 831-4.
-
(2008)
Chem. Pharm. Bull
, vol.56
, pp. 831-834
-
-
Yu, P.F.1
Chen, H.2
Wang, J.3
He, C.X.4
Cao, B.5
Li, M.6
Yang, N.7
Lei, Z.Y.8
Cheng, M.S.9
-
38
-
-
43149126598
-
Design, synthesis, and biological testing of 4β-[(4-substituted)-1,2,3-triazol-1-yl]podophyllotoxin analogues as antitumor agents
-
Reddy, P.B.; Paul, D.V.; Agrawal, S.K.; Saxena, A.K.; Kumar, H.M.S.; Qazi, G.N. Design, synthesis, and biological testing of 4β-[(4-substituted)-1,2,3-triazol-1-yl]podophyllotoxin analogues as antitumor agents. Arch. Pharm. Chem. Life Sci., 2008, 341, 126-31.
-
(2008)
Arch. Pharm. Chem. Life Sci
, vol.341
, pp. 126-131
-
-
Reddy, P.B.1
Paul, D.V.2
Agrawal, S.K.3
Saxena, A.K.4
Kumar, H.M.S.5
Qazi, G.N.6
-
39
-
-
64049110824
-
Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents
-
Chen, S.W.; Xiang, R.; Liu, J.; Tian X. Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents. Bioorg. Med. Chem., 2009, 17, 3111-7.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 3111-3117
-
-
Chen, S.W.1
Xiang, R.2
Liu, J.3
Tian, X.4
-
40
-
-
77649183584
-
First synthesis and biological evaluation of novel spin-labeled derivatives of deoxypodophyllotoxin
-
Zhang, Z.W.; Zhang, J.Q.; Hui, L.; Chen, S.W.; Tian, X. First synthesis and biological evaluation of novel spin-labeled derivatives of deoxypodophyllotoxin. Eur. J. Med. Chem., 2010, 45, 1673-7.
-
(2010)
Eur. J. Med. Chem
, vol.45
, pp. 1673-1677
-
-
Zhang, Z.W.1
Zhang, J.Q.2
Hui, L.3
Chen, S.W.4
Tian, X.5
-
41
-
-
72049120386
-
Synthesis and biological evaluation of novel thiocolchicinepodophyllotoxin conjugates
-
Passarella, D.; Peretto, B.; Yepes, R.B.; Cappelletti, G.; Cartelli, D.; Ronchi, C.; Snaith, J.; Fontana, G.; Danieli, B.; Borlak, J. Synthesis and biological evaluation of novel thiocolchicinepodophyllotoxin conjugates. Eur. J. Med. Chem., 2010, 45, 219-26.
-
(2010)
Eur. J. Med. Chem
, vol.45
, pp. 219-226
-
-
Passarella, D.1
Peretto, B.2
Yepes, R.B.3
Cappelletti, G.4
Cartelli, D.5
Ronchi, C.6
Snaith, J.7
Fontana, G.8
Danieli, B.9
Borlak, J.10
|