scholarly journals Phytochemical studies on the aerial parts of Sarcococca hookeriana (Baillon) of Nepalese origin

1970 ◽  
Vol 21 ◽  
pp. 8-15
Author(s):  
Narayan P. Rai ◽  
Bimala Lama ◽  
Shiva P. Subedi ◽  
W. C. Taylor ◽  
M. D. Manandhar
Keyword(s):  
Spectral Analysis ◽  
Oleanolic Acid ◽  
1H Nmr ◽  
13C Nmr ◽  
Chemical Society ◽  
Chloroform Extract ◽  
Hmbc Spectrum ◽  
Aerial Parts ◽  
Phytochemical Studies ◽  
First Time

Two known pregnane type of alkaloids, axillaridine A and spiropachysine, and an unidentified pregane alkaloid along with oleanolic acid and stigmasteryl glucoside have been isolated from chloroform extract of the aerial parts of Sarcococca hookeriana. The structures of the alkaloids are established on the basis of spectral analysis of 1H-NMR, 13C-NMR, HMQC, COSY and HMBC spectrum. All compounds were isolated for the first time from S. hookeriana. So far, species of Sarcococca was not reported to contain spiropachysine which was initially reported as a novel alkaloid from Pachysandra terminalis SIEB. et ZUCC.(Buxaceae).DOI: 10.3126/jncs.v21i0.215Journal of Nepal Chemical Society Vol.21 2006 pp.8-15

scholarly journals A NEW PRENYLATED FLAVANONE FROM THE ARIAL PART OF Orthosiphon stamineus

2010 ◽  
Vol 8 (1) ◽  
pp. 101-103 ◽  
Author(s):  
M. Amzad Hossain ◽  
Atiqur Rahman ◽  
Sun Chul Kang
Keyword(s):  
1H Nmr ◽  
13C Nmr ◽  
Analytical Methods ◽  
Chloroform Extract ◽  
Orthosiphon Stamineus ◽  
First Time

Phytochemical investigations on the chloroform extract of the arial part of Orthosiphon stamineus resulted in isolation of one new prenylated compound 5,7-dimethoxy-3,4′-dihydroxy-3′,8-di-C-prenylflavanone together with four known flavonoids compounds, sinensetin, eupatorin, 5,6,7,4¢-tetramethoxyflavone and 3-hydroxy-5,6,7,4¢-tetramethoxyflavone. The structures were deduced on basis of different analytical methods such as UV, IR, 1H-NMR, 13C-NMR, DEPT, COSY, HMBQ and GC-MS. The prenylated compound is reported for the first time from this plant.   Keywords: Orthosiphon stamineus, prenylated flavanone, flavonoids

scholarly journals Phytochemical constituents of the flowers of Sarcococca coriacea of Nepalese origin

1970 ◽  
Vol 21 ◽  
pp. 1-7 ◽  
Author(s):  
N. P. Rai ◽  
B. B. Adhikari ◽  
Arjun Paudel ◽  
K. Masuda ◽  
R. D. Mckelvey ◽  
...  
Keyword(s):  
Melting Point ◽  
Spectral Data ◽  
Oleanolic Acid ◽  
1H Nmr ◽  
13C Nmr ◽  
Chemical Society ◽  
Chromatographic Technique ◽  
Sugar Alcohol ◽  
Steroidal Glycosides ◽  
Phytochemical Constituents

From the flowers of Sarcococca coriacea, a triterpenoic acid, oleanolic acid, a pentahydric sugar alcohol, xylitol along with the mixture of steroidal glycosides, stigmasterol-3-O-β-D-glucopyranoside and β-sitosterol-3-O-β-D-glucopyranoside have been isolated by chromatographic technique. Their structures were established on the basis of IR, 1H-NMR, 13C-NMR, spectral data as well as melting point and Co-TLC comparison with the authentic samples. DOI: 10.3126/jncs.v21i0.214Journal of Nepal Chemical Society Vol.21 2006 p.1-7

scholarly journals New isoquinoline alkaloid from Carduus crispus L.

2014 ◽  
Vol 12 ◽  
pp. 85-87
Author(s):  
J Tunsag ◽  
G Davaakhuu ◽  
D Batsuren
Keyword(s):  
1H Nmr ◽  
Bioactive Compounds ◽  
13C Nmr ◽  
Ethanol Extract ◽  
Isoquinoline Alkaloid ◽  
Spectroscopic Methods ◽  
Aerial Parts ◽  
Isolated Compound ◽  
First Time

A new isoquinoline alkaloid, along with other known 4 bioactive compounds (1 isoquinoline alkaloid, 2 flavonoids, 1 coumarin), were isolated from the ethanol extract of aerial parts of Carduus crispus L. Crispine А N-oxide was newly isolated compound, two of them (quercetin and rutin) were compounds isolated for the first time from indicated plant. The structures of these compounds were elucidated and confirmed with spectroscopic methods e.g. 1H-NMR, 13C-NMR, EI-MS, COSY, HSQC, HMBC, and by comparison with literature data.DOI: http://dx.doi.org/10.5564/mjc.v12i0.178 Mongolian Journal of Chemistry Vol.12 2011: 85-87

scholarly journals PHYTOCHEMICAL STUDIES OF THE PETROLEUM ETHER EXTRACT OF THE LEAVES OF Lagerstroemia speciosa Linn

2010 ◽  
Vol 9 (3) ◽  
pp. 500-504
Author(s):  
S.M. Mizanur Rahman ◽  
Shayla Pervin ◽  
Md. Abdul Quader ◽  
M. Amzad Hossain
Keyword(s):  
Petroleum Ether ◽  
1H Nmr ◽  
13C Nmr ◽  
Mass Spectra ◽  
Petroleum Ether Extract ◽  
Ether Extract ◽  
Lagerstroemia Speciosa ◽  
New Compounds ◽  
Phytochemical Studies ◽  
First Time

Two new compounds, normal alcohol containing of higher carbons and isomer of β-sitosterol were isolated for the first time from the petroleum extract of the leaves of Lagerstroemia speciosa. The structure of the compound has been established on the basis of UV, IR, 1H-NMR, 13C-NMR and mass spectra and identified as nonanol and isomer of β-sitosterol.   Keywords: Lagerstroemia speciosa, petroleum ether extracts, isolation, 1-nonanol, 2 β-sitostero, spectral analyses.

scholarly journals Cytotoxic Compounds from Endemic Arnebia purpurea

2015 ◽  
Vol 10 (4) ◽  
pp. 1934578X1501000 ◽  
Author(s):  
Merve Yuzbasioglu ◽  
Ayse Kuruuzum-Uz ◽  
Zuhal Guvenalp ◽  
András Simon ◽  
Gábor Tóth ◽  
...  
Keyword(s):  
Oleanolic Acid ◽  
Flavonoid Glycosides ◽  
Cytotoxic Activities ◽  
Aerial Parts ◽  
Isolation And Characterization ◽  
Cytotoxic Compounds ◽  
Standard Doxorubicin ◽  
Murine Fibrosarcoma ◽  
Phytochemical Studies ◽  
First Time

Phytochemical studies of the roots and aerial parts of endemic Arnebia purpurea S. Erik & H. Sumbul resulted in the isolation and characterization of four naphthoquinones [isovalerylalkannin (1), α-methyl- n-butanoyl alkannin (2), acetylalkannin (3), and alkannin (4)], a triterpene derivative [3- O-acetyl-oleanolic acid (5)], a steroid [β-sitosterol (6)], three flavonoid glycosides [isorhamnetin-3- O-rutinoside (7), kaempferol-3- O-rutinoside (8), kaempferol 3- O-(5″-acetyl) apiofuranoside 7- O-rhamnopyranoside (9)] and a phenolic acid [rosmarinic acid (10)]. 3- O-Acetyl-oleanolic acid, isorhamnetin-3- O-rutinoside, kaempferol-3- O-rutinoside, and kaempferol 3- O-(5″-acetyl) apiofuranoside 7- O-rhamnopyranoside are reported from an Arnebia species for the first time. Cytotoxic activities on L929 murine fibrosarcoma cell line of the isolated compounds were investigated using MTT assay. Naphthoquinones (1–4) showed intermediate cytotoxic activity in comparison with the standard, doxorubicin.

scholarly journals Structure Elucidation of an Pentacyclic Triterpenoid and Phenolic from Steam Bark of Vitex Pubescens Vahl

2019 ◽  
Vol 1 (1) ◽  
pp. 68-74
Author(s):  
Lenny Anwar
Keyword(s):  
1H Nmr ◽  
13C Nmr ◽  
Betulinic Acid ◽  
Spectroscopic Data ◽  
Structure Elucidation ◽  
Stem Bark ◽  
Hydroxybenzoic Acid ◽  
Pentacyclic Triterpenoid ◽  
Reported Data ◽  
First Time

Pentacyclic triterpenoid, betulinic acid (1) and phenolic, p-hydroxybenzoic acid (2), had been isolated for the first time from the stem bark of Vitex pubescens Vahl. The structure of compounds 1 and 2 was determined based on the interpretation of spectroscopic data including UV, IR, NMR (1H-NMR, 13C-NMR, HMQC, HMBC, COSY) and MS, as well as by comparison with those reported data.

scholarly journals Secondary metabolites of three endemic Centaurea L. species

2014 ◽  
Vol 79 (11) ◽  
pp. 1355-1362 ◽  
Author(s):  
Vele Tesevic ◽  
Ivana Aljancic ◽  
Slobodan Milosavljevic ◽  
Vlatka Vajs ◽  
Iris Djordjevic ◽  
...  
Keyword(s):  
Quantitative Analysis ◽  
Nmr Spectroscopy ◽  
Secondary Metabolites ◽  
Sesquiterpene Lactone ◽  
1H Nmr ◽  
13C Nmr ◽  
1H Nmr Spectroscopy ◽  
13C Nmr Spectroscopy ◽  
Esi Ms ◽  
Aerial Parts

The aerial parts of three endemic Centaurea L. species, namely C. tomorosii Micevski, C. soskae Hayek and C. galicicae Micevski, afforded sesquiterpene lactone cnicin (1) and seven flavonoids: apigenin (2), isokaempferide (3), hispidulin (4), eupatorin (5), cirsimaritin (6), santaflavone (7) and salvigenin (8). The structures of the isolated compounds were determined by UV, 1H NMR and 13C NMR spectroscopy and HR-ESI-MS spectrometry. 1H NMR spectroscopy was used as a method for quantitative analysis of sesquiterpene lactone cnicin.

scholarly journals Complete 1H-NMR and 13C-NMR spectral analysis of the pairs of 20(S) and 20(R) ginsenosides

2014 ◽  
Vol 38 (3) ◽  
pp. 194-202 ◽  
Author(s):  
Heejung Yang ◽  
Jeom Yong Kim ◽  
Sun Ok Kim ◽  
Young Hyo Yoo ◽  
Sang Hyun Sung
Keyword(s):  
Spectral Analysis ◽  
1H Nmr ◽  
13C Nmr

scholarly journals Alkaloids from Mongolian species of Peganum multisectum (Maxim) Bobrov

2016 ◽  
Vol 16 ◽  
pp. 48-53 ◽  
Author(s):  
S. Javzan ◽  
D. Selenge ◽  
N. Amartuvshin ◽  
D. Nedelcheva ◽  
V Christov ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Gas Chromatography ◽  
13C Nmr ◽  
Gas Chromatography Mass Spectrometry ◽  
Nmr Analysis ◽  
1H And 13C Nmr ◽  
Aerial Parts ◽  
13C Nmr Analysis ◽  
Pure Compounds ◽  
First Time

Alkaloids of the aerial parts of P. multisectum (Maxim) Bobrov (Zygophyllaceae) growing in Mongolia have been studied by capillary Gas Chromatography-Mass Spectrometry (GC-MS) and Column Chromatography (CC). Four compounds comprising of 2-methylquinoline (1), 9-amino-2, 3,5,6,7,8-hexahydro-1H-cyclopenta [b] quinoline (2), vasicinone (3) and harmine (4) have been determined by GC-MS, while harmine (4), peganine (5), deoxypeganine (6), deoxyvasicinone (7) and harmane (8) were isolated as pure compounds by the CC. The structures of the five alkaloids 4, 5, 6, 7 and 8 were elucidated by the MS and 1H and 13C NMR analysis. The alkaloids 1, 2 and 8 were identified for the first time from this species.Mongolian Journal of Chemistry 16 (42), 2015, 48-53

scholarly journals DIPRENYLATED XANTHONE FROM THE STEM BARK OF KANDIS GAJAH (Garcinia griffithii)

2010 ◽  
Vol 8 (1) ◽  
pp. 97-100
Author(s):  
Elfita Elfita ◽  
Supriyatna Supriyatna ◽  
Husen H. Bahti ◽  
Dachriyanus Dachriyanus
Keyword(s):  
1H Nmr ◽  
13C Nmr ◽  
Spectroscopic Data ◽  
Stem Bark ◽  
First Time

A diprenylated xanthone, 1,5-dihydroxy-3-methoxy-4,7-diprenylxanthone (1) had been isolated the first time from the dichloromethane extract of the stem bark of Garcinia griffithii, together with 1,7-dihydroxyxanthone (2) and polyisoprenylated benzophenone, guttiferone I (3). The structure of these compounds were determined on the basis of spectroscopic data including UV, IR,  1H NMR, 13C NMR, HMQC, HMBC and COSY.   Keywords: diprenylated xanthone, 1,5-dihydroxy-3-methoxy-4,7-diprenylxanthone, Garcinia griffithii

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