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Quoted phrase not found in phrase index: "xiphidium coeruleum"
Page 1
Precursor-Directed Synthesis of Apoptosis-Initiating N-Hydroxyalkyl Phenylbenzoisoquinolindione Alkaloids.
Chen Y, Dahse HM, Paetz C, Schneider B. Chen Y, et al. ChemistryOpen. 2022 Dec;11(12):e202200157. doi: 10.1002/open.202200157. ChemistryOpen. 2022. PMID: 36478420 Free PMC article.
A precursor-directed approach to access N-hydroxyalkyl phenylbenzoisoquinolindiones (PBIQs) has been developed. Incubation of plant material of Xiphidium caeruleum with hydroxylamines of various chain lengths (C(2) , C(4) , C(6) , C(8) , C(10) and C(12) ) resulted i …
A precursor-directed approach to access N-hydroxyalkyl phenylbenzoisoquinolindiones (PBIQs) has been developed. Incubation of plant material …
Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion.
Chen Y, Paetz C, Menezes RC, Schneider B. Chen Y, et al. Phytochemistry. 2017 Jan;133:15-25. doi: 10.1016/j.phytochem.2016.10.011. Epub 2016 Nov 2. Phytochemistry. 2017. PMID: 27816177
Phytochemical investigation of root cultures of Xiphidium caeruleum (Haemodoraceae) resulted in the structure elucidation of five previously undescribed phenylphenalenone-type compounds, structure revision of a phenylphenalenone glucoside, and identification of nine …
Phytochemical investigation of root cultures of Xiphidium caeruleum (Haemodoraceae) resulted in the structure elucidation of f …
Precursor-Directed Biosynthesis of Phenylbenzoisoquinolindione Alkaloids and the Discovery of a Phenylphenalenone-Based Plant Defense Mechanism.
Chen Y, Paetz C, Schneider B. Chen Y, et al. J Nat Prod. 2018 Apr 27;81(4):879-884. doi: 10.1021/acs.jnatprod.7b00885. Epub 2018 Mar 6. J Nat Prod. 2018. PMID: 29509420
Phenylbenzoisochromenone glucosides (oxa-phenylphenalenone glucosides) occurring in some phenylphenalenone-producing plants of the Haemodoraceae undergo conversion to phenylbenzoisoquinolindiones (aza-phenylphenalenones) in extracts of Xiphidium caeruleum. Precursor …
Phenylbenzoisochromenone glucosides (oxa-phenylphenalenone glucosides) occurring in some phenylphenalenone-producing plants of the Haemodora …
Organ-specific distribution and non-enzymatic conversions indicate a metabolic network of phenylphenalenones in Xiphidium caeruleum.
Chen Y, Paetz C, Schneider B. Chen Y, et al. Phytochemistry. 2019 Mar;159:30-38. doi: 10.1016/j.phytochem.2018.12.004. Epub 2018 Dec 17. Phytochemistry. 2019. PMID: 30572115
We investigated the organ-specific phytochemistry of the inflorescences, leaves at different stages of senescence, and roots of Xiphidium caeruleum (Haemodoraceae) and elucidated the structure of six undescribed compounds. ...
We investigated the organ-specific phytochemistry of the inflorescences, leaves at different stages of senescence, and roots of Xiphidium
Organ-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum.
Opitz S, Schneider B. Opitz S, et al. Phytochemistry. 2002 Dec;61(7):819-25. doi: 10.1016/s0031-9422(02)00359-x. Phytochemistry. 2002. PMID: 12453574
The distribution pattern of phenylphenalenone-type compounds was investigated in vegetative and reproductive organs of Xiphidium caeruleum. The highest total molar concentration, up to 30 micromol g(-1) fr. wt, was detected in the root tip and the stamen. ...
The distribution pattern of phenylphenalenone-type compounds was investigated in vegetative and reproductive organs of Xiphidium c
Histochemical analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae).
Opitz S, Schnitzler JP, Hause B, Schneider B. Opitz S, et al. Planta. 2003 Mar;216(5):881-9. doi: 10.1007/s00425-002-0941-z. Epub 2002 Nov 30. Planta. 2003. PMID: 12624776
To this end, confocal laser-scanning microscopy, microspectral photometry and high-performance liquid chromatography were used to study the tissue localisation of phenylphenalenone-type compounds in Xiphidium caeruleum Aubl. From the autofluorescence potential of th …
To this end, confocal laser-scanning microscopy, microspectral photometry and high-performance liquid chromatography were used to study the …
Phenylphenalenone-related compounds: chemotaxonomic markers of the haemodoraceae from Xiphidium caeruleum.
Opitz S, Hölscher D, Oldham NJ, Bartram S, Schneider B. Opitz S, et al. J Nat Prod. 2002 Aug;65(8):1122-30. doi: 10.1021/np020083s. J Nat Prod. 2002. PMID: 12193015
Phytochemical analysis of Xiphidium caeruleum, a neotropical member of the family Haemodoraceae, resulted in the isolation and identification of a variety of phenylphenalenone-related compounds. ...
Phytochemical analysis of Xiphidium caeruleum, a neotropical member of the family Haemodoraceae, resulted in the isolation and …
Co-occurrence of phenylphenalenones and flavonoids in Xiphidium caeruleum Aubl. flowers.
Fang J, Hölscher D, Schneider B. Fang J, et al. Phytochemistry. 2012 Oct;82:143-8. doi: 10.1016/j.phytochem.2012.07.005. Epub 2012 Aug 4. Phytochemistry. 2012. PMID: 22867904
A Xiphidium caeruleum flower extract was separated by semi-preparative HPLC into five fractions, from which three flavonoids, two phenylphenalenones and 17 phenylphenalenone-related compounds including five unknown compounds, were isolated and their structures eluci …
A Xiphidium caeruleum flower extract was separated by semi-preparative HPLC into five fractions, from which three flavonoids, …
Pharmacognostic Study, Diuretic Activity and Acute Oral Toxicity of the Leaves of Xiphidium caeruleum Aubl. Collected in Two Different Phenological Stages.
Gutiérrez Gaitén YI, Felipe González A, Scull Lizama R, Núñez Cairo CR, Álvarez Hernández GL, Díaz Masó V, Noa Rodríguez AC, Herrera Isidrón JA, Pieters L, Foubert K, Herrera Isidrón L. Gutiérrez Gaitén YI, et al. Plants (Basel). 2023 Mar 10;12(6):1268. doi: 10.3390/plants12061268. Plants (Basel). 2023. PMID: 36986955 Free PMC article.
Xiphidium caeruleum Aubl. is traditionally used in Cuba as an analgesic, anti-inflammatory, antilithiatic and diuretic remedy. ...
Xiphidium caeruleum Aubl. is traditionally used in Cuba as an analgesic, anti-inflammatory, antilithiatic and diuretic remedy.
HPLC-NMR for tissue-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae).
Schneider B, Paetz C, Hölscher D, Opitz S. Schneider B, et al. Magn Reson Chem. 2005 Sep;43(9):724-8. doi: 10.1002/mrc.1634. Magn Reson Chem. 2005. PMID: 16049956
HPLC-(1)H NMR has been used to study the tissue-specific distribution of phenylphenalenones, polyphenolic natural products of Xiphidium caeruleum, a neotropical member of the Haemodoraceae plant family. The present results provide insight into the occurrence of phen …
HPLC-(1)H NMR has been used to study the tissue-specific distribution of phenylphenalenones, polyphenolic natural products of Xiphidium
12 results