133 related articles for article (PubMed ID: 36331394)
1. Collective Synthesis of Aplysiatoxin/Oscillatoxin Analogues by a Bioinspired Strategy.
Hada K; Araki Y; Nokura Y; Urabe D; Nishikawa T
J Org Chem; 2022 Nov; 87(22):15618-15633. PubMed ID: 36331394
[TBL] [Abstract][Full Text] [Related]
2. Total synthesis and biological evaluation of oscillatoxins D, E, and F.
Araki Y; Hanaki Y; Kita M; Hayakawa K; Irie K; Nokura Y; Nakazaki A; Nishikawa T
Biosci Biotechnol Biochem; 2021 May; 85(6):1371-1382. PubMed ID: 33851985
[TBL] [Abstract][Full Text] [Related]
3. Oscillatoxin I: A New Aplysiatoxin Derivative, from a Marine Cyanobacterium.
Nagai H; Sato S; Iida K; Hayashi K; Kawaguchi M; Uchida H; Satake M
Toxins (Basel); 2019 Jun; 11(6):. PubMed ID: 31234410
[TBL] [Abstract][Full Text] [Related]
4. Neo-debromoaplysiatoxin C, with new structural rearrangement, derived from debromoaplysiatoxin.
Tang YH; Liang TT; Fan TT; Keen LJ; Zhang XD; Xu L; Zhao Q; Zeng R; Han BN
Nat Prod Res; 2020 Aug; 34(15):2151-2156. PubMed ID: 30835553
[TBL] [Abstract][Full Text] [Related]
5. Chemical and biological study of aplysiatoxin derivatives showing inhibition of potassium channel Kv1.5.
Tang YH; Wu J; Fan TT; Zhang HH; Gong XX; Cao ZY; Zhang J; Lin HW; Han BN
RSC Adv; 2019 Mar; 9(14):7594-7600. PubMed ID: 35521179
[TBL] [Abstract][Full Text] [Related]
6. The Asymmetric Total Synthesis and Configuration Confirmation of Aplysiaenal and Nhatrangin A, Truncated Derivatives of Aplysiatoxin and Oscillatoxin.
Morishita M; Hada K; Kita M; Nishikawa T
J Nat Prod; 2023 Apr; 86(4):1033-1041. PubMed ID: 36999535
[TBL] [Abstract][Full Text] [Related]
7. Recent Developments in Total Syntheses of Cephalosporolides, Penisporolides, and Ascospiroketals.
Yao H; Wang J; Tong R
Chem Rec; 2017 Nov; 17(11):1109-1123. PubMed ID: 28272766
[TBL] [Abstract][Full Text] [Related]
8. Nakahara memorial lecture. New classes of tumor promoters: teleocidin, aplysiatoxin, and palytoxin.
Fujiki H; Suganuma M; Tahira T; Yoshioka A; Nakayasu M; Endo Y; Shudo K; Takayama S; Moore RE; Sugimura T
Princess Takamatsu Symp; 1983; 14():37-45. PubMed ID: 6151565
[TBL] [Abstract][Full Text] [Related]
9. Cyclobutenes: At a Crossroad between Diastereoselective Syntheses of Dienes and Unique Palladium-Catalyzed Asymmetric Allylic Substitutions.
Misale A; Niyomchon S; Maulide N
Acc Chem Res; 2016 Nov; 49(11):2444-2458. PubMed ID: 27797480
[TBL] [Abstract][Full Text] [Related]
10. Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium
Kawaguchi M; Satake M; Zhang BT; Xiao YY; Fukuoka M; Uchida H; Nagai H
Molecules; 2020 Jan; 25(3):. PubMed ID: 31978978
[TBL] [Abstract][Full Text] [Related]
11. Production of anatoxin-a and a novel biosynthetic precursor by the cyanobacterium Aphanizomenon issatschenkoi.
Selwood AI; Holland PT; Wood SA; Smith KF; McNabb PS
Environ Sci Technol; 2007 Jan; 41(2):506-10. PubMed ID: 17310714
[TBL] [Abstract][Full Text] [Related]
12. MS/MS-Based Molecular Networking Approach for the Detection of Aplysiatoxin-Related Compounds in Environmental Marine Cyanobacteria.
Ding CYG; Pang LM; Liang ZX; Goh KKK; Glukhov E; Gerwick WH; Tan LT
Mar Drugs; 2018 Dec; 16(12):. PubMed ID: 30551660
[TBL] [Abstract][Full Text] [Related]
13. Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product.
Fuwa H
Mar Drugs; 2016 Mar; 14(4):. PubMed ID: 27023567
[TBL] [Abstract][Full Text] [Related]
14. Design, synthesis, and biological activity of a synthetically accessible analog of aplysiatoxin with an (R)-(-)-carvone-based conformation-controlling unit.
Suzuki Y; Moritoki K; Kajiwara M; Yanagita RC; Kawanami Y; Hanaki Y; Irie K
Biosci Biotechnol Biochem; 2022 Jul; 86(8):1013-1023. PubMed ID: 35648459
[TBL] [Abstract][Full Text] [Related]
15. Stereodivergent routes in organic synthesis: marine natural products, lactones, other natural products, heterocycles and unnatural compounds.
Nájera C; Foubelo F; Sansano JM; Yus M
Org Biomol Chem; 2020 Feb; 18(7):1279-1336. PubMed ID: 32025682
[TBL] [Abstract][Full Text] [Related]
16. Binding mode prediction of aplysiatoxin, a potent agonist of protein kinase C, through molecular simulation and structure-activity study on simplified analogs of the receptor-recognition domain.
Ashida Y; Yanagita RC; Takahashi C; Kawanami Y; Irie K
Bioorg Med Chem; 2016 Sep; 24(18):4218-4227. PubMed ID: 27436807
[TBL] [Abstract][Full Text] [Related]
17.
Cheikh A; Tabka H; Tlili Y; Santulli A; Bouzouaya N; Bouhaouala-Zahar B; Benkhalifa R
Int J Mol Sci; 2019 Apr; 20(9):. PubMed ID: 31035589
[TBL] [Abstract][Full Text] [Related]
18. Natural Product Biosynthetic Diversity and Comparative Genomics of the Cyanobacteria.
Dittmann E; Gugger M; Sivonen K; Fewer DP
Trends Microbiol; 2015 Oct; 23(10):642-652. PubMed ID: 26433696
[TBL] [Abstract][Full Text] [Related]
19. New Strategies in the Efficient Total Syntheses of Polycyclic Natural Products.
Liu W; Hong B; Wang J; Lei X
Acc Chem Res; 2020 Nov; 53(11):2569-2586. PubMed ID: 33136373
[TBL] [Abstract][Full Text] [Related]
20. [Stereocontrolled Total Synthesis of Biologically Active Natural Products].
Hatakeyama S
Yakugaku Zasshi; 2018; 138(2):191-209. PubMed ID: 29386433
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
