Bioactive natural compounds from Prosopis africana and Abies nobili

Jamal Elmezughi; Hafsat Shittu; Carol Clements; Ru Angelie Edrada-Ebel; Veronique Seidel; Alexander Gray

doi:10.7324/JAPS.2013.30308

Bioactive natural compounds from Prosopis africana and Abies nobili

Jamal Elmezughi, Hafsat Shittu, Carol Clements, Ru Angelie Edrada-Ebel, Veronique Seidel, Alexander Gray

Strathclyde Institute Of Pharmacy And Biomedical Sciences

Research output: Contribution to journal › Article

4 Citations (Scopus)

68 Downloads (Pure)

Abstract

Chromatographic procedures from the aerial parts of Abies nobilis and stem barks of Prosopis africana led to the isolation of two (antimicrobial and cytotoxic) compounds. Their structures were established as 7, 3’, 4’-trihydroxy-3-methoxyflavanone and dehydroabietic acid on the basis of spectroscopic techniques.

Original language	English
Pages (from-to)	40-43
Number of pages	4
Journal	Journal of Applied Pharmaceutical Science
Volume	3
Issue number	3
Early online date	30 Mar 2013
DOIs	https://doi.org/10.7324/JAPS.2013.30308
Publication status	Published - Mar 2013

Keywords

Prosopis africana
Abies nobilis
diterpene
flavanone
antimicrobial
cytotoxicity

Access to Document

10.7324/JAPS.2013.30308Licence: CC BY-NC-SA 4.0

Elmezughi-etal-JAPS2013-bioactive-compounds-prosopis-africana-abies-nobiliFinal published version, 139 KBLicence: CC BY-NC-SA 4.0

Cite this

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title = "Bioactive natural compounds from Prosopis africana and Abies nobili",

abstract = "Chromatographic procedures from the aerial parts of Abies nobilis and stem barks of Prosopis africana led to the isolation of two (antimicrobial and cytotoxic) compounds. Their structures were established as 7, 3{\textquoteright}, 4{\textquoteright}-trihydroxy-3-methoxyflavanone and dehydroabietic acid on the basis of spectroscopic techniques. ",

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AU - Clements, Carol

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AU - Seidel, Veronique

AU - Gray, Alexander

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AB - Chromatographic procedures from the aerial parts of Abies nobilis and stem barks of Prosopis africana led to the isolation of two (antimicrobial and cytotoxic) compounds. Their structures were established as 7, 3’, 4’-trihydroxy-3-methoxyflavanone and dehydroabietic acid on the basis of spectroscopic techniques.

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KW - diterpene

KW - flavanone

KW - antimicrobial

KW - cytotoxicity

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