135 related articles for article (PubMed ID: 26207293)
1. Increasing the Diversity of Known Pictet-Spenglerases.
Tanner ME
Chem Biol; 2015 Jul; 22(7):806-7. PubMed ID: 26207293
[TBL] [Abstract][Full Text] [Related]
2. Structural Basis for β-Carboline Alkaloid Production by the Microbial Homodimeric Enzyme McbB.
Mori T; Hoshino S; Sahashi S; Wakimoto T; Matsui T; Morita H; Abe I
Chem Biol; 2015 Jul; 22(7):898-906. PubMed ID: 26120001
[TBL] [Abstract][Full Text] [Related]
3. Pictet-Spenglerases in alkaloid biosynthesis: Future applications in biocatalysis.
Roddan R; Ward JM; Keep NH; Hailes HC
Curr Opin Chem Biol; 2020 Apr; 55():69-76. PubMed ID: 31978651
[TBL] [Abstract][Full Text] [Related]
4. Scaffold tailoring by a newly detected Pictet-Spenglerase activity of strictosidine synthase: from the common tryptoline skeleton to the rare piperazino-indole framework.
Wu F; Zhu H; Sun L; Rajendran C; Wang M; Ren X; Panjikar S; Cherkasov A; Zou H; Stöckigt J
J Am Chem Soc; 2012 Jan; 134(3):1498-500. PubMed ID: 22229634
[TBL] [Abstract][Full Text] [Related]
5. Asymmetric Synthesis of (R)-1-Alkyl-Substituted Tetrahydro-ß-carbolines Catalyzed by Strictosidine Synthases.
Pressnitz D; Fischereder EM; Pletz J; Kofler C; Hammerer L; Hiebler K; Lechner H; Richter N; Eger E; Kroutil W
Angew Chem Int Ed Engl; 2018 Aug; 57(33):10683-10687. PubMed ID: 29852524
[TBL] [Abstract][Full Text] [Related]
6. Strictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzyme.
Maresh JJ; Giddings LA; Friedrich A; Loris EA; Panjikar S; Trout BL; Stöckigt J; Peters B; O'Connor SE
J Am Chem Soc; 2008 Jan; 130(2):710-23. PubMed ID: 18081287
[TBL] [Abstract][Full Text] [Related]
7. Strictosidine synthase, an indispensable enzyme involved in the biosynthesis of terpenoid indole and β-carboline alkaloids.
Cao N; Wang CH
Chin J Nat Med; 2021 Aug; 19(8):591-607. PubMed ID: 34419259
[TBL] [Abstract][Full Text] [Related]
8. [Research progress of Pictet-Spenglerases].
Xie Y; Chen Q; Zhang S; Shen C
Sheng Wu Gong Cheng Xue Bao; 2020 Oct; 36(10):2001-2016. PubMed ID: 33169566
[TBL] [Abstract][Full Text] [Related]
9. Characterization of a new microbial Pictet-Spenglerase NscbB affording the β-carboline skeletons from Nocardiopsis synnemataformans DSM 44143.
Chen Q; Zhang S; Xie Y
J Biotechnol; 2018 Sep; 281():137-143. PubMed ID: 29981450
[TBL] [Abstract][Full Text] [Related]
10. β-Methyltryptamine Provoking the Crucial Role of Strictosidine Synthase Tyr151-OH for Its Stereoselective Pictet-Spengler Reactions to Tryptoline-type Alkaloids.
Liu H; Panjikar S; Sheng X; Futamura Y; Zhang C; Shao N; Osada H; Zou H
ACS Chem Biol; 2022 Jan; 17(1):187-197. PubMed ID: 34994203
[TBL] [Abstract][Full Text] [Related]
11. Direct Biomimetic Synthesis of β-Carboline Alkaloids from Two Amino Acids.
Wang ZX; Xiang JC; Cheng Y; Ma JT; Wu YD; Wu AX
J Org Chem; 2018 Oct; 83(19):12247-12254. PubMed ID: 30134110
[TBL] [Abstract][Full Text] [Related]
12. The biosynthesis of beta-carboline and quinolizidine alkaloids of Alangium lamarckii.
Jain S; Sinha A; Bhakuni DS
Phytochemistry; 2002 Aug; 60(8):853-9. PubMed ID: 12150812
[TBL] [Abstract][Full Text] [Related]
13. Substrate specificity of strictosidine synthase.
McCoy E; Galan MC; O'Connor SE
Bioorg Med Chem Lett; 2006 May; 16(9):2475-8. PubMed ID: 16481164
[TBL] [Abstract][Full Text] [Related]
14. Structural basis of enzymatic (S)-norcoclaurine biosynthesis.
Ilari A; Franceschini S; Bonamore A; Arenghi F; Botta B; Macone A; Pasquo A; Bellucci L; Boffi A
J Biol Chem; 2009 Jan; 284(2):897-904. PubMed ID: 19004827
[TBL] [Abstract][Full Text] [Related]
15. Enhancement of 5-aminopenta-2,4-dienals electrophilicity via activation by O,N-bistrifluoroacetylation. application to an N-acyl Pictet-Spengler reaction.
Nuhant P; Raikar SB; Wypych JC; Delpech B; Marazano C
J Org Chem; 2009 Dec; 74(24):9413-21. PubMed ID: 19924881
[TBL] [Abstract][Full Text] [Related]
16. Collision-induced dissociation actualized the H+-promoted reaction as observed in vitro; harman formation from beta-carboline-type monoterpenoid glucoindole alkaloids.
Aimi N; Kitajima M; Yokoya M; Takayama H; Sakamoto S; Yamaguchi K
Chem Pharm Bull (Tokyo); 2002 Nov; 50(11):1528-9. PubMed ID: 12419926
[TBL] [Abstract][Full Text] [Related]
17. Application of Pictet-Spengler Reaction to Indole-Based Alkaloids Containing Tetrahydro-β-carboline Scaffold in Combinatorial Chemistry.
Rao RN; Maiti B; Chanda K
ACS Comb Sci; 2017 Apr; 19(4):199-228. PubMed ID: 28276678
[TBL] [Abstract][Full Text] [Related]
18. Why are the terpenoid indole alkaloids of type I homochiral?
Beke G; Patthy-Lukáts A ; Podányi B; Szabó LF
Chirality; 2001 Aug; 13(8):483-7. PubMed ID: 11466772
[TBL] [Abstract][Full Text] [Related]
19. A comprehensive overview of β-carbolines and its derivatives as anticancer agents.
Luo B; Song X
Eur J Med Chem; 2021 Nov; 224():113688. PubMed ID: 34332400
[TBL] [Abstract][Full Text] [Related]
20. Review of β-carboline alkaloids from the genus Aspidosperma.
Layne TH; Roach JS; Tinto WF
Nat Prod Commun; 2015 Jan; 10(1):183-6. PubMed ID: 25920243
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]