193 related articles for article (PubMed ID: 35011453)
1. Design and Synthesis of Novel Podophyllotoxins Hybrids and the Effects of Different Functional Groups on Cytotoxicity.
Yang Z; Zhou Z; Luo X; Luo X; Luo H; Luo L; Yang W
Molecules; 2021 Dec; 27(1):. PubMed ID: 35011453
[TBL] [Abstract][Full Text] [Related]
2. 4β-[(4-Alkyl)-1,2,3-triazol-1-yl] podophyllotoxins as anticancer compounds: design, synthesis and biological evaluation.
Reddy DM; Srinivas J; Chashoo G; Saxena AK; Sampath Kumar HM
Eur J Med Chem; 2011 Jun; 46(6):1983-91. PubMed ID: 21477899
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of d-ring modified acid hydrazide derivatives of podophyllotoxin and their anticancer studies as Tubulin inhibiting agents.
Nerella S; Kankala S; Paidakula S; Gavaji B
Bioorg Chem; 2020 Jan; 94():103384. PubMed ID: 31776036
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and biological evaluation of 4beta-[(4-substituted)-1,2,3-triazol-1-yl]podophyllotoxins as potential anticancer agents.
Reddy PB; Agrawal SK; Singh S; Bhat BA; Saxena AK; Kumar HM; Qazi GN
Chem Biodivers; 2008 Sep; 5(9):1792-802. PubMed ID: 18816530
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents.
Liu Y; Wei D; Zhao Y; Cheng W; Lu Y; Ma Y; Li X; Han C; Wei Y; Cao H; Zhao C
Bioorg Med Chem; 2012 Nov; 20(21):6285-95. PubMed ID: 23022053
[TBL] [Abstract][Full Text] [Related]
6. Toward synthesis of third-generation spin-labeled podophyllotoxin derivatives using isocyanide multicomponent reactions.
Kou L; Wang MJ; Wang LT; Zhao XB; Nan X; Yang L; Liu YQ; Morris-Natschke SL; Lee KH
Eur J Med Chem; 2014 Mar; 75():282-8. PubMed ID: 24553146
[TBL] [Abstract][Full Text] [Related]
7. Synthesis and Biological evaluation of novel 4β-[(5-substituted)-1,2,3,4-tetrazolyl] podophyllotoxins as anticancer compounds.
Hyder I; Yedlapudi D; Kalivendi SV; Khazir J; Ismail T; Nalla N; Miryala S; Sampath Kumar HM
Bioorg Med Chem Lett; 2015 Jul; 25(14):2860-3. PubMed ID: 26022842
[TBL] [Abstract][Full Text] [Related]
8. Synthesis and biological evaluation of podophyllotoxin congeners as tubulin polymerization inhibitors.
Kamal A; Srinivasa Reddy T; Polepalli S; Shalini N; Reddy VG; Subba Rao AV; Jain N; Shankaraiah N
Bioorg Med Chem; 2014 Oct; 22(19):5466-75. PubMed ID: 25131956
[TBL] [Abstract][Full Text] [Related]
9. Synthesis and anticancer activity of dimeric podophyllotoxin derivatives.
Zi CT; Yang L; Xu FQ; Dong FW; Yang D; Li Y; Ding ZT; Zhou J; Jiang ZH; Hu JM
Drug Des Devel Ther; 2018; 12():3393-3406. PubMed ID: 30349193
[TBL] [Abstract][Full Text] [Related]
10. Design, synthesis and potent cytotoxic activity of novel podophyllotoxin derivatives.
Li WQ; Wang XL; Qian K; Liu YQ; Wang CY; Yang L; Tian J; Morris-Natschke SL; Zhou XW; Lee KH
Bioorg Med Chem; 2013 Apr; 21(8):2363-2369. PubMed ID: 23490151
[TBL] [Abstract][Full Text] [Related]
11. Studies on novel 4beta-[(4-substituted)-1,2,3-triazol-1-yl] podophyllotoxins as potential anticancer agents.
Bhat BA; Reddy PB; Agrawal SK; Saxena AK; Kumar HM; Qazi GN
Eur J Med Chem; 2008 Oct; 43(10):2067-72. PubMed ID: 17988764
[TBL] [Abstract][Full Text] [Related]
12. N-hydroxyethyl-4-aza-didehydropodophyllotoxin derivatives as potential antitumor agents.
Kumar A; Kumar V; Alegria AE; Malhotra SV
Eur J Pharm Sci; 2011 Sep; 44(1-2):21-6. PubMed ID: 21601635
[TBL] [Abstract][Full Text] [Related]
13. Design and synthesis of 4β-Acetamidobenzofuranone-podophyllotoxin hybrids and their anti-cancer evaluation.
Paidakula S; Nerella S; Vadde R; Kamal A; Kankala S
Bioorg Med Chem Lett; 2019 Aug; 29(16):2153-2156. PubMed ID: 31281022
[TBL] [Abstract][Full Text] [Related]
14. Synthesis of novel potent cytotoxicy podophyllotoxin-naphthoquinone compounds via microwave-assited multicomponent domino reactions.
Nguyen Thi QG; Le-Nhat-Thuy G; Dang Thi TA; Hoang Thi P; Nguyen Tuan A; Nguyen Thi TH; Nguyen TT; Nguyen Ha T; Hoang Mai H; Nguyen TV
Bioorg Med Chem Lett; 2021 Apr; 37():127841. PubMed ID: 33556568
[TBL] [Abstract][Full Text] [Related]
15. Recent Advances in the Application of Podophyllotoxin Derivatives to Fight Against Multidrug-Resistant Cancer Cells.
Guo Q; Jiang E
Curr Top Med Chem; 2021; 21(19):1712-1724. PubMed ID: 33441065
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of podophyllotoxin linked β-carboline congeners as potential anticancer agents and DNA topoisomerase II inhibitors.
Sathish M; Kavitha B; Nayak VL; Tangella Y; Ajitha A; Nekkanti S; Alarifi A; Shankaraiah N; Nagesh N; Kamal A
Eur J Med Chem; 2018 Jan; 144():557-571. PubMed ID: 29289881
[TBL] [Abstract][Full Text] [Related]
17. One-pot synthesis and biological evaluation of N-(aminosulfonyl)-4-podophyllotoxin carbamates as potential anticancer agents.
Xu XH; Guan XW; Feng SL; Ma YZ; Chen SW; Hui L
Bioorg Med Chem Lett; 2017 Jul; 27(13):2890-2894. PubMed ID: 28512026
[TBL] [Abstract][Full Text] [Related]
18. Podophyllotoxin derivatives as an excellent anticancer aspirant for future chemotherapy: A key current imminent needs.
Zhang X; Rakesh KP; Shantharam CS; Manukumar HM; Asiri AM; Marwani HM; Qin HL
Bioorg Med Chem; 2018 Jan; 26(2):340-355. PubMed ID: 29269253
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of podophyllotoxin-glycosyl triazoles
Nerella S; Kankala S; Gavaji B
Nat Prod Res; 2021 Jan; 35(1):9-16. PubMed ID: 31210060
[TBL] [Abstract][Full Text] [Related]
20. Multicomponent assembly of 4-aza-podophyllotoxins: A fast entry to highly selective and potent anti-leukemic agents.
Jeedimalla N; Flint M; Smith L; Haces A; Minond D; Roche SP
Eur J Med Chem; 2015 Dec; 106():167-79. PubMed ID: 26547055
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
