These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 23427901)

  • 1. Absolute configurations of fungal and plant metabolites by chiroptical methods. ORD, ECD, and VCD studies on phyllostin, scytolide, and oxysporone.
    Mazzeo G; Santoro E; Andolfi A; Cimmino A; Troselj P; Petrovic AG; Superchi S; Evidente A; Berova N
    J Nat Prod; 2013 Apr; 76(4):588-99. PubMed ID: 23427901
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absolute configurations of phytotoxins seiricardine A and inuloxin A obtained by chiroptical studies.
    Santoro E; Mazzeo G; Petrovic AG; Cimmino A; Koshoubu J; Evidente A; Berova N; Superchi S
    Phytochemistry; 2015 Aug; 116():359-366. PubMed ID: 25817835
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Importance and Difficulties in the Use of Chiroptical Methods to Assign the Absolute Configuration of Natural Products: The Case of Phytotoxic Pyrones and Furanones Produced by Diplodia corticola.
    Mazzeo G; Cimmino A; Masi M; Longhi G; Maddau L; Memo M; Evidente A; Abbate S
    J Nat Prod; 2017 Sep; 80(9):2406-2415. PubMed ID: 28901768
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stereochemistry of the tadalafil diastereoisomers: a critical assessment of vibrational circular dichroism, electronic circular dichroism, and optical rotatory dispersion.
    Qiu S; De Gussem E; Tehrani KA; Sergeyev S; Bultinck P; Herrebout W
    J Med Chem; 2013 Nov; 56(21):8903-14. PubMed ID: 24116968
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assignment Through Chiroptical Methods of The Absolute Configuration of Fungal Dihydropyranpyran-4-5-Diones Phytotoxins, Potential Herbicides for Buffelgrass (
    Santoro E; Mazzeo G; Marsico G; Masi M; Longhi G; Superchi S; Evidente A; Abbate S
    Molecules; 2019 Aug; 24(17):. PubMed ID: 31438466
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absolute configuration of an axially chiral sulfonate determined from its optical rotatory dispersion, electronic circular dichroism, and vibrational circular dichroism spectra.
    Covington CL; Raghavan V; Smuts JP; Armstrong DW; Polavarapu PL
    Chirality; 2017 Nov; 29(11):670-676. PubMed ID: 28833487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Determination of the absolute configurations of natural products via density functional theory calculations of vibrational circular dichroism, electronic circular dichroism, and optical rotation: the iridoids plumericin and isoplumericin.
    Stephens PJ; Pan JJ; Devlin FJ; Krohn K; Kurtán T
    J Org Chem; 2007 Apr; 72(9):3521-36. PubMed ID: 17388636
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absolute Configuration of (-)-Centratherin, a Sesquiterpenoid Lactone, Defined by Means of Chiroptical Spectroscopy.
    Junior FM; Covington CL; de Albuquerque AC; Lobo JF; Borges RM; de Amorim MB; Polavarapu PL
    J Nat Prod; 2015 Nov; 78(11):2617-23. PubMed ID: 26565920
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Determining the absolute configuration of two marine compounds using vibrational chiroptical spectroscopy.
    Hopmann KH; Šebestík J; Novotná J; Stensen W; Urbanová M; Svenson J; Svendsen JS; Bouř P; Ruud K
    J Org Chem; 2012 Jan; 77(2):858-69. PubMed ID: 22148737
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Absolute Configuration of a Rare Sesquiterpene: (+)-3-Ishwarone.
    Junior FM; Covington CL; de Amorim MB; Velozo LS; Kaplan MA; Polavarapu PL
    J Nat Prod; 2014 Aug; 77(8):1881-6. PubMed ID: 25051336
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Determination of the absolute configurations of bicyclo[3.1.0]hexane derivatives via electronic circular dichroism, optical rotation dispersion and vibrational circular dichroism spectroscopy and density functional theory calculations.
    Yang G; Li J; Liu Y; Lowary TL; Xu Y
    Org Biomol Chem; 2010 Aug; 8(16):3777-83. PubMed ID: 20567790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chiroptical studies on brevianamide B: vibrational and electronic circular dichroism confronted.
    Bultinck P; Cherblanc FL; Fuchter MJ; Herrebout WA; Lo YP; Rzepa HS; Siligardi G; Weimar M
    J Org Chem; 2015 Apr; 80(7):3359-67. PubMed ID: 25734916
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Study on the absolute configuration of levetiracetam via density functional theory calculations of electronic circular dichroism and optical rotatory dispersion.
    Li L; Si YK
    J Pharm Biomed Anal; 2011 Nov; 56(3):465-70. PubMed ID: 21794998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enantiomeric 4-Acylamino-6-alkyloxy-2 Alkylthiopyrimidines As Potential A3 Adenosine Receptor Antagonists: HPLC Chiral Resolution and Absolute Configuration Assignment by a Full Set of Chiroptical Spectroscopy.
    Rossi D; Nasti R; Marra A; Meneghini S; Mazzeo G; Longhi G; Memo M; Cosimelli B; Greco G; Novellino E; Da Settimo F; Martini C; Taliani S; Abbate S; Collina S
    Chirality; 2016 May; 28(5):434-40. PubMed ID: 27095007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absolute configuration assignment to anticancer Amaryllidaceae alkaloid jonquailine.
    Vergura S; Santoro E; Masi M; Evidente A; Scafato P; Superchi S; Mazzeo G; Longhi G; Abbate S
    Fitoterapia; 2018 Sep; 129():78-84. PubMed ID: 29928968
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Determination of the absolute configurations of natural products via density functional theory calculations of vibrational circular dichroism, electronic circular dichroism and optical rotation: the schizozygane alkaloid schizozygine.
    Stephens PJ; Pan JJ; Devlin FJ; Urbanová M; Hájícek J
    J Org Chem; 2007 Mar; 72(7):2508-24. PubMed ID: 17338574
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination of the absolute configurations of natural products via density functional theory calculations of optical rotation, electronic circular dichroism, and vibrational circular dichroism: the cytotoxic sesquiterpene natural products quadrone, suberosenone, suberosanone, and suberosenol A acetate.
    Stephens PJ; McCann DM; Devlin FJ; Smith AB
    J Nat Prod; 2006 Jul; 69(7):1055-64. PubMed ID: 16872144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A single chiroptical spectroscopic method may not be able to establish the absolute configurations of diastereomers: dimethylesters of hibiscus and garcinia acids.
    Polavarapu PL; Donahue EA; Shanmugam G; Scalmani G; Hawkins EK; Rizzo C; Ibnusaud I; Thomas G; Habel D; Sebastian D
    J Phys Chem A; 2011 Jun; 115(22):5665-73. PubMed ID: 21568330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Absolute Configuration Determination by Quantum Mechanical Calculation of Chiroptical Spectra: Basics and Applications to Fungal Metabolites.
    Superchi S; Scafato P; Gorecki M; Pescitelli G
    Curr Med Chem; 2018; 25(2):287-320. PubMed ID: 28294053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epimeric Mixture Analysis and Absolute Configuration Determination Using an Integrated Spectroscopic and Computational Approach-A Case Study of Two Epimers of 6-Hydroxyhippeastidine.
    Le NT; Vermeyen T; Aerts R; Herrebout WA; Pieters L; Tuenter E
    Molecules; 2022 Dec; 28(1):. PubMed ID: 36615407
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.