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Folium Sennae protects against hydroxyl radical-induced DNA damage via antioxidant mechanism: an in vitro study.

Botanical studies

Lin J, Li X, Han L, Li F, Lu W, Bai Y, Chen D.
PMID: 28510920
Bot Stud. 2014 Dec;55(1):16. doi: 10.1186/1999-3110-55-16. Epub 2014 Feb 02.

BACKGROUND: In the study, Folium Sennae (FS) was firstly extracted by various solvents to obtain five FS extracts. Then, five FS extracts were evaluated for the protective effects against •OH-induced DNA damage, antioxidant abilities in vitro, and chemical contents...

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Lin J, Li X, Han L, et al. Folium Sennae protects against hydroxyl radical-induced DNA damage via antioxidant mechanism: an in vitro study. Bot Stud. 2014;55(1):16doi: 10.1186/1999-3110-55-16.
Lin, J., Li, X., Han, L., Li, F., Lu, W., Bai, Y., & Chen, D. (2014). Folium Sennae protects against hydroxyl radical-induced DNA damage via antioxidant mechanism: an in vitro study. Botanical studies, 55(1), 16. https://doi.org/10.1186/1999-3110-55-16
Lin, Jian, et al. "Folium Sennae protects against hydroxyl radical-induced DNA damage via antioxidant mechanism: an in vitro study." Botanical studies vol. 55,1 (2014): 16. doi: https://doi.org/10.1186/1999-3110-55-16
Lin J, Li X, Han L, Li F, Lu W, Bai Y, Chen D. Folium Sennae protects against hydroxyl radical-induced DNA damage via antioxidant mechanism: an in vitro study. Bot Stud. 2014 Dec;55(1):16. doi: 10.1186/1999-3110-55-16. Epub 2014 Feb 02. PMID: 28510920; PMCID: PMC5430338.
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Anti-plasmodial activity of ethanolic extract of root and stem back of Cassia sieberiana DC on mice.

Journal of intercultural ethnopharmacology

Abdulrazak N, Asiya UI, Usman NS, Unata IM, Farida A.
PMID: 26401393
J Intercult Ethnopharmacol. 2015 Apr-Jun;4(2):96-101. doi: 10.5455/jice.20141231014333. Epub 2015 Jan 20.

AIM: This study assessed within 4 days of suppressive test in vivo antimalarial activity of Ethanolic extract of root and stem bark of Cassia sieberiana DC against chloroquine sensitive strain of Plasmodium berghei NK65 in mice.METHODOLOGY: Two sets, each...

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Abdulrazak N, Asiya UI, Usman NS, et al. Anti-plasmodial activity of ethanolic extract of root and stem back of Cassia sieberiana DC on mice. J Intercult Ethnopharmacol. 2015;4(2):96-101doi: 10.5455/jice.20141231014333.
Abdulrazak, N., Asiya, U. I., Usman, N. S., Unata, I. M., & Farida, A. (2015). Anti-plasmodial activity of ethanolic extract of root and stem back of Cassia sieberiana DC on mice. Journal of intercultural ethnopharmacology, 4(2), 96-101. https://doi.org/10.5455/jice.20141231014333
Abdulrazak, Nuhu, et al. "Anti-plasmodial activity of ethanolic extract of root and stem back of Cassia sieberiana DC on mice." Journal of intercultural ethnopharmacology vol. 4,2 (2015): 96-101. doi: https://doi.org/10.5455/jice.20141231014333
Abdulrazak N, Asiya UI, Usman NS, Unata IM, Farida A. Anti-plasmodial activity of ethanolic extract of root and stem back of Cassia sieberiana DC on mice. J Intercult Ethnopharmacol. 2015 Apr-Jun;4(2):96-101. doi: 10.5455/jice.20141231014333. Epub 2015 Jan 20. PMID: 26401393; PMCID: PMC4566778.
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Combined TDDFT and AIM Insights into Photoinduced Excited State Intramolecular Proton Transfer (ESIPT) Mechanism in Hydroxyl- and Amino-Anthraquinone Solution.

Scientific reports

Zheng D, Zhang M, Zhao G.
PMID: 29062001
Sci Rep. 2017 Oct 23;7(1):13766. doi: 10.1038/s41598-017-14094-5.

Time-dependent density functional theory (TDDFT) and atoms in molecules (AIM) theory are combined to study the photoinduced excited state intramolecular proton transfer (ESIPT) dynamics for eight anthraquinones (AQs) derivatives in solution. The calculated absorption and emission spectra are consistent...

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Zheng D, Zhang M, Zhao G. Combined TDDFT and AIM Insights into Photoinduced Excited State Intramolecular Proton Transfer (ESIPT) Mechanism in Hydroxyl- and Amino-Anthraquinone Solution. Sci Rep. 2017;7(1):13766doi: 10.1038/s41598-017-14094-5.
Zheng, D., Zhang, M., & Zhao, G. (2017). Combined TDDFT and AIM Insights into Photoinduced Excited State Intramolecular Proton Transfer (ESIPT) Mechanism in Hydroxyl- and Amino-Anthraquinone Solution. Scientific reports, 7(1), 13766. https://doi.org/10.1038/s41598-017-14094-5
Zheng, Daoyuan, et al. "Combined TDDFT and AIM Insights into Photoinduced Excited State Intramolecular Proton Transfer (ESIPT) Mechanism in Hydroxyl- and Amino-Anthraquinone Solution." Scientific reports vol. 7,1 (2017): 13766. doi: https://doi.org/10.1038/s41598-017-14094-5
Zheng D, Zhang M, Zhao G. Combined TDDFT and AIM Insights into Photoinduced Excited State Intramolecular Proton Transfer (ESIPT) Mechanism in Hydroxyl- and Amino-Anthraquinone Solution. Sci Rep. 2017 Oct 23;7(1):13766. doi: 10.1038/s41598-017-14094-5. PMID: 29062001; PMCID: PMC5653788.
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Food Value of Two Varieties of Ginger (Zingiber officinale) Commonly Consumed in Nigeria.

ISRN nutrition

Ajayi OB, Akomolafe SF, Akinyemi FT.
PMID: 24967255
ISRN Nutr. 2013 Jan 17;2013:359727. doi: 10.5402/2013/359727. eCollection 2013.

Ginger (Zingiber officinale) is a well-known and widely used herb, which contains several interesting bioactive constituents and possesses health-promoting properties. The proximate, mineral, antinutrient, amino acid, and phytochemical components of two varieties of ginger (Zingiber officinale) were investigated. Amino...

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Ajayi OB, Akomolafe SF, Akinyemi FT. Food Value of Two Varieties of Ginger (Zingiber officinale) Commonly Consumed in Nigeria. ISRN Nutr. 2013;2013:359727doi: 10.5402/2013/359727.
Ajayi, O. B., Akomolafe, S. F., & Akinyemi, F. T. (2013). Food Value of Two Varieties of Ginger (Zingiber officinale) Commonly Consumed in Nigeria. ISRN nutrition, 2013359727. https://doi.org/10.5402/2013/359727
Ajayi, Olubunmi B, et al. "Food Value of Two Varieties of Ginger (Zingiber officinale) Commonly Consumed in Nigeria." ISRN nutrition vol. 2013 (2013): 359727. doi: https://doi.org/10.5402/2013/359727
Ajayi OB, Akomolafe SF, Akinyemi FT. Food Value of Two Varieties of Ginger (Zingiber officinale) Commonly Consumed in Nigeria. ISRN Nutr. 2013 Jan 17;2013:359727. doi: 10.5402/2013/359727. eCollection 2013. PMID: 24967255; PMCID: PMC4045280.
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Identification and characterization of the ergochrome gene cluster in the plant pathogenic fungus .

Fungal biology and biotechnology

Neubauer L, Dopstadt J, Humpf HU, Tudzynski P.
PMID: 28955461
Fungal Biol Biotechnol. 2016 Mar 22;3:2. doi: 10.1186/s40694-016-0020-z. eCollection 2016.

RESULTS: This study identified the gene cluster responsible for the synthesis of the ergot pigments. Overexpression of the cluster-specific transcription factor led to activation of the gene cluster and to the production of several known ergot pigments. Knock out...

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Neubauer L, Dopstadt J, Humpf HU, et al. Identification and characterization of the ergochrome gene cluster in the plant pathogenic fungus . Fungal Biol Biotechnol. 2016;3:2doi: 10.1186/s40694-016-0020-z.
Neubauer, L., Dopstadt, J., Humpf, H. U., & Tudzynski, P. (2016). Identification and characterization of the ergochrome gene cluster in the plant pathogenic fungus . Fungal biology and biotechnology, 32. https://doi.org/10.1186/s40694-016-0020-z
Neubauer, Lisa, et al. "Identification and characterization of the ergochrome gene cluster in the plant pathogenic fungus ." Fungal biology and biotechnology vol. 3 (2016): 2. doi: https://doi.org/10.1186/s40694-016-0020-z
Neubauer L, Dopstadt J, Humpf HU, Tudzynski P. Identification and characterization of the ergochrome gene cluster in the plant pathogenic fungus . Fungal Biol Biotechnol. 2016 Mar 22;3:2. doi: 10.1186/s40694-016-0020-z. eCollection 2016. PMID: 28955461; PMCID: PMC5611617.
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Antibacterial activities and structure-activity relationships of a panel of 48 compounds from Kenyan plants against multidrug resistant phenotypes.

SpringerPlus

Omosa LK, Midiwo JO, Mbaveng AT, Tankeo SB, Seukep JA, Voukeng IK, Dzotam JK, Isemeki J, Derese S, Omolle RA, Efferth T, Kuete V.
PMID: 27386347
Springerplus. 2016 Jun 27;5(1):901. doi: 10.1186/s40064-016-2599-1. eCollection 2016.

In the current study forty eight compounds belonging to anthraquinones, naphthoquinones, benzoquinones, flavonoids (chalcones and polymethoxylated flavones) and diterpenoids (clerodanes and kauranes) were explored for their antimicrobial potential against a panel of sensitive and multi-drug resistant Gram-negative and Gram-positive...

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Omosa LK, Midiwo JO, Mbaveng AT, et al. Antibacterial activities and structure-activity relationships of a panel of 48 compounds from Kenyan plants against multidrug resistant phenotypes. Springerplus. 2016;5(1):901doi: 10.1186/s40064-016-2599-1.
Omosa, L. K., Midiwo, J. O., Mbaveng, A. T., Tankeo, S. B., Seukep, J. A., Voukeng, I. K., Dzotam, J. K., Isemeki, J., Derese, S., Omolle, R. A., Efferth, T., & Kuete, V. (2016). Antibacterial activities and structure-activity relationships of a panel of 48 compounds from Kenyan plants against multidrug resistant phenotypes. SpringerPlus, 5(1), 901. https://doi.org/10.1186/s40064-016-2599-1
Omosa, Leonidah K, et al. "Antibacterial activities and structure-activity relationships of a panel of 48 compounds from Kenyan plants against multidrug resistant phenotypes." SpringerPlus vol. 5,1 (2016): 901. doi: https://doi.org/10.1186/s40064-016-2599-1
Omosa LK, Midiwo JO, Mbaveng AT, Tankeo SB, Seukep JA, Voukeng IK, Dzotam JK, Isemeki J, Derese S, Omolle RA, Efferth T, Kuete V. Antibacterial activities and structure-activity relationships of a panel of 48 compounds from Kenyan plants against multidrug resistant phenotypes. Springerplus. 2016 Jun 27;5(1):901. doi: 10.1186/s40064-016-2599-1. eCollection 2016. PMID: 27386347; PMCID: PMC4923020.
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Evaluation of the palatability of chrysomelid larvae containing anthraquinones to birds.

Oecologia

Hilker M, Köpf A.
PMID: 28306931
Oecologia. 1994 Dec;100(4):421-429. doi: 10.1007/BF00317864.

Chrysomelid larvae of the subfamily Galerucinae, tribe Galerucini, are known to contain 1,8-dihydroxylated 9,10-anthraquinones. Since nonhydroxylated 9,10-anthraquinone is the active agent in several commercial products sold to protect seeds against birds, we suggested that the naturally occurring dihydroxylated anthraquinones...

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Hilker M, Köpf A. Evaluation of the palatability of chrysomelid larvae containing anthraquinones to birds. Oecologia. 1994;100(4):421-429doi: 10.1007/BF00317864.
Hilker, M., & Köpf, A. (1994). Evaluation of the palatability of chrysomelid larvae containing anthraquinones to birds. Oecologia, 100(4), 421-429. https://doi.org/10.1007/BF00317864
Hilker, Monika, and Köpf, Alfred. "Evaluation of the palatability of chrysomelid larvae containing anthraquinones to birds." Oecologia vol. 100,4 (1994): 421-429. doi: https://doi.org/10.1007/BF00317864
Hilker M, Köpf A. Evaluation of the palatability of chrysomelid larvae containing anthraquinones to birds. Oecologia. 1994 Dec;100(4):421-429. doi: 10.1007/BF00317864. PMID: 28306931.
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Lipophilic Constituents of Rumex vesicarius L. and Rumex dentatus L.

Antioxidants (Basel, Switzerland)

Elfotoh MA, Shams KA, Anthony KP, Shahat AA, Ibrahim MT, Abdelhady NM, Azim NS, Hammouda FM, El-Missiry MM, Saleh MA.
PMID: 26784344
Antioxidants (Basel). 2013 Sep 16;2(3):167-80. doi: 10.3390/antiox2030167.

Rumex dentatus L. and Rumex vesicarius L., of the family Polygonaceae, are edible herbs growing wild in Egypt. Their lipoid constituents were examined by both liquid chromatography/mass spectrometry (LC/MS) and by gas chromatography/mass spectrometry (GC/MS). Their essential oil compositions...

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Elfotoh MA, Shams KA, Anthony KP, et al. Lipophilic Constituents of Rumex vesicarius L. and Rumex dentatus L. Antioxidants (Basel). 2013;2(3):167-80doi: 10.3390/antiox2030167.
Elfotoh, M. A., Shams, K. A., Anthony, K. P., Shahat, A. A., Ibrahim, M. T., Abdelhady, N. M., Azim, N. S., Hammouda, F. M., El-Missiry, M. M., & Saleh, M. A. (2013). Lipophilic Constituents of Rumex vesicarius L. and Rumex dentatus L. Antioxidants (Basel, Switzerland), 2(3), 167-80. https://doi.org/10.3390/antiox2030167
Elfotoh, Mona A Abou, et al. "Lipophilic Constituents of Rumex vesicarius L. and Rumex dentatus L." Antioxidants (Basel, Switzerland) vol. 2,3 (2013): 167-80. doi: https://doi.org/10.3390/antiox2030167
Elfotoh MA, Shams KA, Anthony KP, Shahat AA, Ibrahim MT, Abdelhady NM, Azim NS, Hammouda FM, El-Missiry MM, Saleh MA. Lipophilic Constituents of Rumex vesicarius L. and Rumex dentatus L. Antioxidants (Basel). 2013 Sep 16;2(3):167-80. doi: 10.3390/antiox2030167. PMID: 26784344; PMCID: PMC4665437.
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Anthraquinones in different developmental stages ofGaleruca tanaceti (Coleoptera, Chrysomelidae).

Journal of chemical ecology

Hilker M, Schulz S.
PMID: 24258609
J Chem Ecol. 1991 Nov;17(11):2323-32. doi: 10.1007/BF00988011.

The overwintering eggs and the larvae of the leaf beetleGaleruca tanaceti (L.) contain hydroxylated anthraquinones. In both developmental stages, l,8-dihydroxy-3-methylanthraquinone (= chrysophanol) and 1,8-di-hydroxyanthraquinone (= chrysazin) were detected by GC-MS and GC-FTIR analyses. In the eggs, chrysazin was found...

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Hilker M, Schulz S. Anthraquinones in different developmental stages ofGaleruca tanaceti (Coleoptera, Chrysomelidae). J Chem Ecol. 1991;17(11):2323-32doi: 10.1007/BF00988011.
Hilker, M., & Schulz, S. (1991). Anthraquinones in different developmental stages ofGaleruca tanaceti (Coleoptera, Chrysomelidae). Journal of chemical ecology, 17(11), 2323-32. https://doi.org/10.1007/BF00988011
Hilker, M, and Schulz, S. "Anthraquinones in different developmental stages ofGaleruca tanaceti (Coleoptera, Chrysomelidae)." Journal of chemical ecology vol. 17,11 (1991): 2323-32. doi: https://doi.org/10.1007/BF00988011
Hilker M, Schulz S. Anthraquinones in different developmental stages ofGaleruca tanaceti (Coleoptera, Chrysomelidae). J Chem Ecol. 1991 Nov;17(11):2323-32. doi: 10.1007/BF00988011. PMID: 24258609.
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Characterisation of historical organic dyestuffs by liquid chromatography-mass spectrometry.

Analytical and bioanalytical chemistry

Rosenberg E.
PMID: 18398605
Anal Bioanal Chem. 2008 May;391(1):33-57. doi: 10.1007/s00216-008-1977-0. Epub 2008 Apr 09.

This review discusses the characterisation of natural organic dyestuffs of historical interest by liquid chromatography-mass spectrometry. The structures of the most important natural organic dyestuffs traditionally used are presented and discussed from the perspective of their analytical chemical determination....

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Rosenberg E. Characterisation of historical organic dyestuffs by liquid chromatography-mass spectrometry. Anal Bioanal Chem. 2008;391(1):33-57doi: 10.1007/s00216-008-1977-0.
Rosenberg, E. (2008). Characterisation of historical organic dyestuffs by liquid chromatography-mass spectrometry. Analytical and bioanalytical chemistry, 391(1), 33-57. https://doi.org/10.1007/s00216-008-1977-0
Rosenberg, Erwin. "Characterisation of historical organic dyestuffs by liquid chromatography-mass spectrometry." Analytical and bioanalytical chemistry vol. 391,1 (2008): 33-57. doi: https://doi.org/10.1007/s00216-008-1977-0
Rosenberg E. Characterisation of historical organic dyestuffs by liquid chromatography-mass spectrometry. Anal Bioanal Chem. 2008 May;391(1):33-57. doi: 10.1007/s00216-008-1977-0. Epub 2008 Apr 09. PMID: 18398605.
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The Site of the Inhibition of the Shikimate Pathway by Glyphosate: II. INTERFERENCE OF GLYPHOSATE WITH CHORISMATE FORMATION IN VIVO AND IN VITRO.

Plant physiology

Amrhein N, Deus B, Gehrke P, Steinrücken HC.
PMID: 16661535
Plant Physiol. 1980 Nov;66(5):830-4. doi: 10.1104/pp.66.5.830.

In the presence of the nonselective herbicide glyphosate (N-[phosphonomethyl]glycine), buckwheat (Fagopyrum esculentum Moench) hypocotyls and cultured cells of Galium mollugo L. accumulate an organic acid, which was identified as shikimate by mass-spectroscopy of its methyl ester. After growth in...

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Amrhein N, Deus B, Gehrke P, et al. The Site of the Inhibition of the Shikimate Pathway by Glyphosate: II. INTERFERENCE OF GLYPHOSATE WITH CHORISMATE FORMATION IN VIVO AND IN VITRO. Plant Physiol. 1980;66(5):830-4doi: 10.1104/pp.66.5.830.
Amrhein, N., Deus, B., Gehrke, P., & Steinrücken, H. C. (1980). The Site of the Inhibition of the Shikimate Pathway by Glyphosate: II. INTERFERENCE OF GLYPHOSATE WITH CHORISMATE FORMATION IN VIVO AND IN VITRO. Plant physiology, 66(5), 830-4. https://doi.org/10.1104/pp.66.5.830
Amrhein, N, et al. "The Site of the Inhibition of the Shikimate Pathway by Glyphosate: II. INTERFERENCE OF GLYPHOSATE WITH CHORISMATE FORMATION IN VIVO AND IN VITRO." Plant physiology vol. 66,5 (1980): 830-4. doi: https://doi.org/10.1104/pp.66.5.830
Amrhein N, Deus B, Gehrke P, Steinrücken HC. The Site of the Inhibition of the Shikimate Pathway by Glyphosate: II. INTERFERENCE OF GLYPHOSATE WITH CHORISMATE FORMATION IN VIVO AND IN VITRO. Plant Physiol. 1980 Nov;66(5):830-4. doi: 10.1104/pp.66.5.830. PMID: 16661535; PMCID: PMC440735.
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Quantitative structure-property relationship study of acidity constants of some 9,10-anthraquinone derivatives using multiple linear regression and partial least-squares procedures.

Talanta

Shamsipur M, Hemmateenejad B, Akhond M, Sharghi H.
PMID: 18968333
Talanta. 2001 Jul 06;54(6):1113-20. doi: 10.1016/s0039-9140(01)00374-5.

A quantitative structure-property relationship study is suggested for the prediction of acidity constants of some recently synthesized 9,10-anthraquinone derivatives in binary methanol-water mixtures. Modeling of the acidity constant of the anthraquinones as a function of physicochemical parameters and mole...

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Shamsipur M, Hemmateenejad B, Akhond M, et al. Quantitative structure-property relationship study of acidity constants of some 9,10-anthraquinone derivatives using multiple linear regression and partial least-squares procedures. Talanta. 2001;54(6):1113-20doi: 10.1016/s0039-9140(01)00374-5.
Shamsipur, M., Hemmateenejad, B., Akhond, M., & Sharghi, H. (2001). Quantitative structure-property relationship study of acidity constants of some 9,10-anthraquinone derivatives using multiple linear regression and partial least-squares procedures. Talanta, 54(6), 1113-20. https://doi.org/10.1016/s0039-9140(01)00374-5
Shamsipur, M, et al. "Quantitative structure-property relationship study of acidity constants of some 9,10-anthraquinone derivatives using multiple linear regression and partial least-squares procedures." Talanta vol. 54,6 (2001): 1113-20. doi: https://doi.org/10.1016/s0039-9140(01)00374-5
Shamsipur M, Hemmateenejad B, Akhond M, Sharghi H. Quantitative structure-property relationship study of acidity constants of some 9,10-anthraquinone derivatives using multiple linear regression and partial least-squares procedures. Talanta. 2001 Jul 06;54(6):1113-20. doi: 10.1016/s0039-9140(01)00374-5. PMID: 18968333.
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Showing 1 to 12 of 310 entries