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1.
Indian J Nephrol ; 23(3): 180-3, 2013 May.
Article in English | MEDLINE | ID: mdl-23814415

ABSTRACT

In patients with acute kidney injury (AKI), serum creatinine level does not increase until moderate to severe reduction in glomerular filtration rate (GFR) occurs. Thus its use for estimating GFR in early AKI delays detection of kidney damage and making important therapeutic decisions. Moreover, serum cystatin C is not affected by gender, age, race, and muscle mass and also does not suffer from lag period for its rise in early AKI. We studied 200 healthy subjects and 130 AKI patients over a period of 2 years at a tertiary care hospital. Serum creatinine and serum cystatin C were studied and analyzed in relevance to early AKI. We found that 56.2% of patients of AKI group had normal levels of serum creatinine in early phase, while all patients had elevated serum cystatin C at same time. Multiple logistic regression analysis revealed cystatin C-based GFR reflecting decline in GFR with worsening AKI in better than creatinine-based GFR. Serum cystatin C is a better marker of renal function in early stages of AKI and is less affected by age, gender, muscle mass, and ethnicity. Its use helps in early therapeutic intervention and possibly favorable outcome.

2.
Nat Prod Res ; 24(1): 63-7, 2010.
Article in English | MEDLINE | ID: mdl-20013474

ABSTRACT

A new benzylisoquinoline alkaloid, argemexirine, together with two known protoberberine alkaloids, dl-tetrahydrocoptisine and dihydrocoptisine, have been isolated from the methanolic extract of the whole plant of Argemone mexicana L. The compounds were identified by spectral and chemical evidence. This is the first report of these alkaloids in this plant species.


Subject(s)
Alkaloids/chemistry , Argemone/chemistry , Isoquinolines/chemistry , Alkaloids/isolation & purification , Berberine/analogs & derivatives , Berberine/chemistry , Isoquinolines/isolation & purification , Magnetic Resonance Spectroscopy , Methanol , Methylation , Plant Extracts/analysis , Solvents , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet
3.
Nat Prod Res ; 23(17): 1599-602, 2009.
Article in English | MEDLINE | ID: mdl-19851925

ABSTRACT

A new indole alkaloid, N-formylscholarine, together with picrinine, strictamine and nareline has been isolated from the fruit pods of Alstonia scholaris, and their structures were established by various spectral data. This is the first report of these alkaloids in A. scholaris fruit pods.


Subject(s)
Alstonia/chemistry , Indole Alkaloids/chemistry , Alkaloids/chemistry , Alkaloids/isolation & purification , Fruit/chemistry , Indole Alkaloids/isolation & purification , Magnetic Resonance Spectroscopy , Molecular Structure
4.
Folia Microbiol (Praha) ; 54(3): 204-6, 2009.
Article in English | MEDLINE | ID: mdl-19649736

ABSTRACT

The isoquinoline alkaloids hunnemanine and norsanguinarine have been isolated from methanolic extract of the whole plant of Eschscholzia californica. These two alkaloids were checked for their antifungal activity against phytopathogenic fungi Alternaria melongenae, A. brassicola, A. brassicae, Curvularia lunata, C. maculans, Helminthosporium pennisetti, H. oryzae, H. turcicum, Fusarium undum and F. lini. Hunnemanine exhibited 100 % inhibition of spore germination of A. brassicae, H. pennisetti and F. lini at 1000 ppm whereas norsanguinarine exhibited 100 % inhibition of A. brassicicola and C. maculans at this concentration.


Subject(s)
Alkaloids/pharmacology , Antifungal Agents/pharmacology , Eschscholzia/chemistry , Fungi/drug effects , Isoquinolines/pharmacology , Morphine Derivatives/pharmacology , Alkaloids/chemistry , Alkaloids/isolation & purification , Antifungal Agents/chemistry , Antifungal Agents/isolation & purification , Isoquinolines/chemistry , Isoquinolines/isolation & purification , Morphine Derivatives/chemistry , Morphine Derivatives/isolation & purification , Plant Extracts/chemistry
5.
Nat Prod Res ; 22(18): 1657-9, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19085424

ABSTRACT

A new chalcone glycoside, chalcone-2',4-dihydroxy-4'-O-beta-D-glucoside has been isolated from Rhamnus nipalensis together with sitosterol, lupeol, di-O-methyldaidzein, kaempferol-4'-methylether, quercetin, physcion, sitosterol glucoside, emodin and their structures established by spectroscopic data. Isolation of these compounds are the first report from this plant.


Subject(s)
Chalcones/isolation & purification , Glucosides/isolation & purification , Plants, Medicinal/chemistry , Rhamnus/chemistry , Chalcones/chemistry , Emodin/analogs & derivatives , Emodin/isolation & purification , Glucosides/chemistry , India , Kaempferols/isolation & purification , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Pentacyclic Triterpenes , Quercetin/isolation & purification , Sitosterols/isolation & purification , Triterpenes/isolation & purification
6.
Nat Prod Res ; 22(6): 533-6, 2008 Apr 15.
Article in English | MEDLINE | ID: mdl-18415862

ABSTRACT

A new alkaloid, fuyuziphine together with (+/-)-alpha-hydrastine has been isolated from the whole plant of Fumaria indica. The structures of these alkaloids have been established by spectral and chemical evidences.


Subject(s)
Alkaloids/chemistry , Fumaria/chemistry , Isoquinolines/chemistry , Alkaloids/isolation & purification , Isoquinolines/isolation & purification , Mass Spectrometry , Nuclear Magnetic Resonance, Biomolecular , Optical Rotation , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Spectrophotometry, Infrared
7.
Mycobiology ; 35(2): 69-71, 2007 Jun.
Article in English | MEDLINE | ID: mdl-24015073

ABSTRACT

1-Corydalmine,an alkaloid isolated from roots of Corydalis chaerophylla inhibited spore germination of some plant pathogenic as well as saprophytic fungi e.g. Alternaria brassicae, A. brassicicola, A. solani, Curvularia lunata, C. maculans, C. sp., C. pallscens, Erysiphe pisi, Fusarium udum, Helminthosporium species,H. penniseti and a Heterosporium species. 1-Corydalmine significantly inhibited spore germination of all the fungi at 100 to 1500 ppm. It was effective against all the fungi at 1500 ppm. C. lunata was highly sensitive to this chemical even at 250 ppm.

8.
J Asian Nat Prod Res ; 8(8): 733-7, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17145662

ABSTRACT

Two new cyclopeptide alkaloids, sativanine-N and sativanine-O were isolated from the stem bark of Zizyphussativa and their structures were established by spectral analysis.


Subject(s)
Alkaloids/chemistry , Peptides, Cyclic/chemistry , Plant Bark/chemistry , Ziziphus/chemistry , Alkaloids/isolation & purification , Chromatography , India , Molecular Structure , Peptides, Cyclic/isolation & purification , Spectrophotometry
9.
J Asian Nat Prod Res ; 8(3): 197-200, 2006.
Article in English | MEDLINE | ID: mdl-16864424

ABSTRACT

A new isoflavone glycoside, echinoside (7), together with 7-hydroxyisoflavone, kaempferol-4'-methylether, kaempferol-7-methylether, myrecetin-3-O-alpha-L-rhamnoside, kaempferol and kaempferol-3-O-alpha-L-rhamnoside, has been isolated from the whole plant of Echinops echinatus. The structure of echinoside has been established by chemical and spectral data. This is the first report of the occurrence of these flavonoids in E. echinatus.


Subject(s)
Echinops Plant/chemistry , Flavonoids/chemistry , Flavonoids/isolation & purification , Molecular Structure
10.
Mycobiology ; 34(3): 120-3, 2006 Sep.
Article in English | MEDLINE | ID: mdl-24039483

ABSTRACT

Phytoterpenoid isolated from Artabotrytis odoratissimus inhibited spore germination of some plant pathogenic as well as saprophytic fungi e.g. Alternaria alternata, A. solani, Cercospora sp., Curvularia maculans, C. pennisetti, Fusarium udum, Helminthosporium echinochlova, H. frumentacie, H. penniseti and Ustilago cynodontis. In Curvularia maculans and H. frumentacie, spore germination was completely inhibited at 2000 ppm. However, Curvularia maculans and C. pennisetti showed considerable sensitivity to this chemical even at 500 ppm.

11.
Mycobiology ; 33(2): 97-103, 2005 Jun.
Article in English | MEDLINE | ID: mdl-24049481

ABSTRACT

Crude extracts and active principles from medicinal plants have shown potential role in controlling plant diseases in glasshouses as well as in fields as one of the safest and ecofriendly methods. The effect of nor-securinine (an alkaloid) isolated from Phyllanthus amarus has been seen against spore germination of some fungi (Alternaria brassicae, A. solani, Curvularia pennisetti, Curvularia sp., Erysiphe pisi, Helminthosporium frumentacei) as well as pea powdery mildew (Erysiphe pisi) under glasshouse conditions. The sensitivity of fungi to nor-securinine varied considerably. Nor-securinine was effective against most of the fungi. H. frumentacei was more sensitive even at the lowest concentration (1,000 µg/ml). Likewise conidia of E. pisi were also inhibited in partially or completely appressorium formation. Pre-inoculation treatment showed greater efficacy than post-inoculation in inhibiting powdery mildew development on pea plants in a glasshouse. Maximum inhibition occurred at 2000 µg/ml.

12.
Mycobiology ; 33(4): 206-9, 2005 Dec.
Article in English | MEDLINE | ID: mdl-24049502

ABSTRACT

Narceine methyl ester and narceine are potent alkaloids which were isolated from Corydalis longipes were found effective in vitro at very low concentration, i.e., 100~500 ppm against spore germination of some test plant pathogenic fungi (Alternaria solani, A. tagetica, Cercospora abelmoschi, Curvularia maculans, Erysiphe cichoracearum, E. pisi, Fusarium udum, Helminthosporium oryzae, H. penniseti, Ustilago cynodontis). Among the test, phytopathogens the spores of F. udum, C. maculans and H. penniseti were highly sensitive at 200 ppm. However, spores of E. pisi, A. solani and A. tagetica were less sensitive at low concentration followed by other test fungi. Most of the fungi showed zero or nearly zero percent spore germination at 400 and 500 ppm.

13.
Folia Microbiol (Praha) ; 48(3): 363-8, 2003.
Article in English | MEDLINE | ID: mdl-12879748

ABSTRACT

(+/-)-alpha-Hydrastine and (+/-)-beta-hydrastine were isolated from Corydalis longipes; both exhibited considerable efficacy against spore germination of some saprophytic and phytopathogenic fungi. While (+/-)-alpha-hydrastine was effective against most of the fungi, Helminthosporium echinoclova was least affected even at the highest dose (150 ppm). (+/-)-beta-Hydrastine was equally effective against several fungi. Mixture of both compounds was more effective than each one individually. Helminthosporium species were again the most resistant toward the mixture. The effect of both alkaloids independently on germination and development of E. pisi conidia on excised pea leaves was also shown. After pre-inoculation with (+/-)-alpha-hydrastine, the effect was more pronounced than the addition post-inoculation; maximum inhibition occurred at 200 ppm. (+/-)-beta-Hydrastine also reduced germination of conidia but was less effective than (+/-)-alpha-hydrastine. The number of primary and secondary branches of conidia and number of appressoria were not affected significantly by either compound.


Subject(s)
Alkaloids/pharmacology , Antifungal Agents/pharmacology , Mitosporic Fungi/drug effects , Plant Diseases/microbiology , Benzylisoquinolines , Corydalis/microbiology , Germination/drug effects , Mitosporic Fungi/growth & development , Pest Control, Biological/methods , Plant Leaves/microbiology , Spores, Fungal/drug effects , Spores, Fungal/growth & development
14.
Folia Microbiol (Praha) ; 48(5): 605-9, 2003.
Article in English | MEDLINE | ID: mdl-14976716

ABSTRACT

The alkaloids N-methylhydrasteine hydroxylactam and 1-methoxyberberine chloride were isolated from Corydalis longipes. Both alkaloids showed high efficacy individually (in concentration of 50-150 ppm) and also in a 1:1 mixture against spore germination of some fungi, viz. Alternaria alternata, A. brassicae, Curvularia maculans, Curvularia sp., Colletotrichum gloeosporioides, Colletotrichum sp., Helminthosporium speciferum, H. pennisetti, Helminthosporium sp., and Ustilago cynodontis. The antifungal effect of single compounds was dose-dependent. If the mutual ratio of the two components in the mixture was changed from 1:1 to a major content of any of the two compounds, the inhibitory effect on spore germination decreased.


Subject(s)
Alkaloids/chemistry , Antifungal Agents/chemistry , Corydalis/chemistry , Alkaloids/isolation & purification , Alkaloids/pharmacology , Antifungal Agents/isolation & purification , Antifungal Agents/pharmacology , Fungi/drug effects , Fungi/growth & development , Plant Preparations/chemistry , Spores, Fungal/drug effects
15.
Phytother Res ; 16(4): 393-4, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12112301

ABSTRACT

Plumieride has been isolated as an active principle of the leaves of Allamanda cathartica. It showed strong fungitoxicity against some dermatophytes causing dermatomycosis to animals and human beings. It exhibited a noncytotoxic nature against a P(388) mouse leukaemia cell line.


Subject(s)
Antifungal Agents/isolation & purification , Antifungal Agents/pharmacology , Apocynaceae/chemistry , Dermatomycoses/pathology , Furans/isolation & purification , Furans/pharmacology , Spiro Compounds/isolation & purification , Spiro Compounds/pharmacology , Animals , Antifungal Agents/chemistry , Cell Division/drug effects , Epidermophyton/drug effects , Furans/chemistry , Humans , Inhibitory Concentration 50 , Leukemia P388/pathology , Mice , Microsporum/drug effects , Molecular Structure , Plant Extracts/chemistry , Plant Leaves/chemistry , Spiro Compounds/chemistry , Tumor Cells, Cultured
16.
Folia Microbiol (Praha) ; 47(3): 287-90, 2002.
Article in English | MEDLINE | ID: mdl-12094740

ABSTRACT

Inhibition activity of the alkaloid (-)-corypalmine on spore germination of plant pathogenic and saprophytic fungi (Alternaria solani, A brassicicola, A. brassicae, A. melongenae, Curvularia pallescens, C. lunata, C. maculans, Curvularisa sp., Colletotrichum sp., Helminthosporium speciferum, H. frumentacei, H. pennisetti, Heterosporium sp., Penicillum sp., Ustilago cynodontis) was determined. Spore germination of all the tested fungi was inhibited, Heterosporium sp. and Ustilago cynodontis being the most sensitive (complete inhibition of spore germination was observed at the very low concentration of 200 ppm). Curvularia palliscens, C. maculans and Curvularia sp. were less sensitive; complete inhibition of spore germination occurred at 400 ppm.


Subject(s)
Alkaloids/chemistry , Alkaloids/pharmacology , Antifungal Agents/pharmacology , Fungi/drug effects , Heterocyclic Compounds, 4 or More Rings/pharmacology , Spores, Fungal/drug effects , Alkaloids/isolation & purification , Antifungal Agents/isolation & purification , Fungi/physiology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Species Specificity
17.
Folia Microbiol (Praha) ; 47(2): 161-5, 2002.
Article in English | MEDLINE | ID: mdl-12058395

ABSTRACT

Berberine and (+/-)-bicuculline were isolated from roots and leaves, respectively, of Corydalis chaerophylla. Both were effective in vitro against spore germination of some plant pathogenic fungi (Alternaria brassicicola, A. brassicae, A. cheiranthi, A. melongenae, A. solani, Colletotrichum musae, C. falcatum, Curvularia penniseti, C. lunata, C. maculans, C. pallescens, Curvularia sp., Erysiphe pisi, E. cichoracearum, Erysiphe sp., Fusarium udum, Helminthosporium spiciferum, H. penniseti, H. frumentacei, Heterosporium sp., Oidium erysiphoides and Ustilago cynodontis). Berberine and (+/-)-bicuculline significantly inhibited spore germination of all the fungi at concentrations of 100-1000 ppm. Berberine was effective against all the fungi at all concentrations; most of the fungi did not germinate at 1000 ppm. H. penniseti conidia did not germinate at any concentration of (+/-)-bicuculline. U. cynodontis was the least sensitive fungus at lower concentrations but 800 ppm dose was highly effective.


Subject(s)
Antifungal Agents/pharmacology , Berberine/pharmacology , Bicuculline/pharmacology , Corydalis/chemistry , Antifungal Agents/isolation & purification , Plants, Medicinal/chemistry , Spores, Fungal/drug effects , Spores, Fungal/growth & development
18.
J Ethnopharmacol ; 79(1): 69-73, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11744297

ABSTRACT

A toxicological study was performed in albino mice and rat with methanolic extract and isolated alkaloid of Taxus baccata Linn. (family: Taxaceae). LD(50) study showed the higher toxic activity in stem (TXA-1,2,3) as compared with leaf (TXB-1,2,3) extract. As the extract were further fractionated into crude alkaloids and purified by chromatography the toxicity of these fractions were found to be in increasing order as follows: methanolic extract (1) < crude alkaloidal fraction (2) < purified alkaloidal fraction (3). The effects of leaf and stem extract of T. baccata were studied on certain biochemical and haematological parameters of mice and rat after 10, 20 and 30 days of exposure. Among the parameters examined, the exposed animal exhibited significant decrease in total leukocyte count (TLC), lymphocytes and cholesterol level (mg/dl), whereas increase was observed in serum transminases (SGOT, SGPT) and alkaline phosphatase (AP) of TXA-1 and TXB-1 treated groups indicating toxic conditions associated due to liver involvement.


Subject(s)
Anticarcinogenic Agents/toxicity , Bridged-Ring Compounds/toxicity , Taxoids , Animals , Anticarcinogenic Agents/isolation & purification , Bridged-Ring Compounds/isolation & purification , Female , Lethal Dose 50 , Male , Mice , Plant Leaves , Plant Stems , Rats , Taxus
19.
J Asian Nat Prod Res ; 3(3): 207-12, 2001.
Article in English | MEDLINE | ID: mdl-11491396

ABSTRACT

A new triterpene glycoside, arjunetoside, together with oleanolic and arjunic acids has been isolated from the root bark of Terminalia arjuna. The structure of arjunetoside has been established as 3-O-beta-D-glucopyranosyl-2alpha,3beta, 19alpha-trihydroxyolean-12-en-28-oic acid, 28-O-beta-D-glucopyranoside by chemical and spectral data.


Subject(s)
Glycosides/isolation & purification , Plant Extracts/isolation & purification , Terminalia/chemistry , Triterpenes/isolation & purification , Chromatography, Thin Layer , Glycosides/chemistry , India , Magnetic Resonance Spectroscopy , Mass Spectrometry , Methylation , Molecular Structure , Oleanolic Acid/chemistry , Oleanolic Acid/isolation & purification , Plant Extracts/chemistry , Plant Roots/chemistry , Plants, Medicinal/chemistry , Spectrophotometry, Infrared , Triterpenes/chemistry
20.
J Asian Nat Prod Res ; 3(3): 213-7, 2001.
Article in English | MEDLINE | ID: mdl-11491397

ABSTRACT

From the whole plant of Eclipta alba, a new triterpene saponin, named eclalbatin, together with alpha-amyrin, ursolic acid and oleanolic acid were isolated. The structure of eclalbatin has been established as 3-O-beta-D-glucopyranosyl-3-beta-hydroxy-olean-12-en-28-oic acid, 28-O-beta-D-arabinopyranoside (1) on the basis of chemical and spectral data.


Subject(s)
Asteraceae/chemistry , Plant Extracts/isolation & purification , Saponins/isolation & purification , Triterpenes/isolation & purification , Chromatography, Thin Layer , India , Mass Spectrometry , Medicine, Traditional , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Oleanolic Acid/chemistry , Oleanolic Acid/isolation & purification , Plant Extracts/chemistry , Plants, Medicinal/chemistry , Saponins/chemistry , Spectrophotometry, Infrared , Triterpenes/chemistry , Ursolic Acid
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