scholarly journals Two New Sesquiterpenes from Laurus azorica

2001 ◽  
Vol 56 (7-8) ◽  
pp. 503-505 ◽  
Author(s):  
Braulio M. Fraga ◽  
Inmaculada Cabrera ◽  
Matías Reina ◽  
David Terrero
Keyword(s):  
Spectroscopic Methods ◽  
Aerial Parts ◽  
Laurus Azorica

The structures of a new eudesmane sesquiterpene, lauradiol, and a new secoeudesmane, azoridione, have been determined by spectroscopic methods. These compounds and the known sesquiterpenic alcohols, clovanediol and caryophyllenol II, have been isolated from the aerial parts of Laurus azorica

scholarly journals 30-Normedicagenic Acid Glycosides from Chenopodium Foliosum

2012 ◽  
Vol 7 (11) ◽  
pp. 1934578X1200701
Author(s):  
Paraskev T. Nedialkov ◽  
Zlatina Kokanova-Nedialkova ◽  
Daniel Bücherl ◽  
Georgi Momekov ◽  
Jörg Heilmann ◽  
...  
Keyword(s):  
Methyl Ester ◽  
Cell Lines ◽  
Interleukin 2 ◽  
Leukemic Cell ◽  
2D Nmr ◽  
Spectroscopic Methods ◽  
Dioic Acid ◽  
Leukemic Cell Lines ◽  
Aerial Parts

Two new glycosides of 30-normedicagenic acid, namely 3- O-[ β-D-glucuronopyranosyl methyl ester]-2 β,3 β-dihydroxy-30-noroleane-12,20(29)-diene-23,28-dioic acid 28- O-β-D-glucopyranosyl ester, and 3- O-β-D-glucopyranosyl-2 β,3 β-dihydroxy-30-noroleane-12,20(29)-diene-23,28-dioic acid, together with the known 3- O-β-glucopyranosyl-2 β,3 β-dihydroxy-30-noroleane-12,20(29)-diene-23,28-dioic acid 28- O-β-glucopyranosyl ester, and 3- O-β-glucuronopyranosyl-2 β,3 β-dihydroxy-30-noroleane-12,20(29)-diene-23,28-dioic acid 28- O-β-glucopyranosyl ester were isolated from the aerial parts of Chenopodium foliosum Asch. The structures of the compounds were determined by means of spectroscopic methods (1D and 2D NMR, UV, IR) and HRMS-ESI. The compounds were tested for cytotoxicity on three leukemic cell lines (BV-173, SKW-3, HL-60). In addition, the saponins showed moderate stimulatory effects on interleukin-2 production in PHA/PMA stimulated Jurkat E6.1 cells.

scholarly journals Phenolic Constituents of Knautia arvensis Aerial Parts

2011 ◽  
Vol 6 (11) ◽  
pp. 1934578X1100601 ◽  
Author(s):  
Jaroslaw Moldoch ◽  
Barbara Szajwaj ◽  
Milena Masullo ◽  
Lukasz Pecio ◽  
Wieslaw Oleszek ◽  
...  
Keyword(s):  
Chlorogenic Acid ◽  
2D Nmr ◽  
Spectroscopic Methods ◽  
Flavone Glycoside ◽  
Aerial Parts ◽  
Dicaffeoylquinic Acid ◽  
Phenolic Constituents ◽  
First Time

A new C-6 flavone glycoside (6), together with seven known compounds, cryptochlorogenic acid (1), chlorogenic acid (2), 2- O- trans-caffeoylhydrocitric acid (3), isovitexin 7-β-D-glucopyranoside (4), 7,4′-dihydroxy-5-methoxyflavone-6- C-β-D-glucopyranoside (5), 3,5- O-dicaffeoylquinic acid (7) and 4,5- O-dicaffeoylquinic acid (8), were isolated from the aerial parts of Knautia arvensis. Their structures were elucidated by extensive spectroscopic methods including 1D- (1H, 13C and TOCSY) and 2D-NMR (DQF-COSY, HSQC, HMBC) experiments, as well as ESIMS analysis. Compounds 1, 3-5 and 8 are reported for the first time in Knautia arvensis.

Flavon- and Flavonolglycosides from Achillea pannonica Scheele

2001 ◽  
Vol 56 (7-8) ◽  
pp. 521-525 ◽  
Author(s):  
Denata Kasaj ◽  
Liselotte Krenn ◽  
Sonja Prinz ◽  
Antje Hüfner ◽  
Shi Shan Yuc ◽  
...  
Keyword(s):  
Methanolic Extract ◽  
2D Nmr ◽  
Flavonoid Glycosides ◽  
Spectroscopic Methods ◽  
Esi Ms ◽  
Aerial Parts ◽  
Nmr Techniques ◽  
Chemotaxonomic Study ◽  
First Time ◽  
C Nmr

The detailed investigation of a methanolic extract of aerial parts of Achillea pannonica SCHEELE. within a chemotaxonomic study led to the isolation of 6 flavonoid glycosides. Besides rutin, apigenin-7-O-glucopyranoside, luteolin-7-O-glucopyranoside, apigenin-7-O-rutinoside and acacetin-7-O-rutinoside, an unusual flavondiglucoside was isolated. Its structure was established by UV, 1HNMR and 13C NMR spectroscopic methods including 2D-NMR techniques and ESI-MS as luteolin-7,4′-O-β-diglucoside. This substance is reported for the first time in the genus Achillea. Chemotaxonomic aspects are discussed briefly

Dryopterin, ein neuartiges C17-Flavan aus Dryopteris filix-mas / Dryopterin, a Novel C17-Flavan from Dryopteris filix-mas

1981 ◽  
Vol 36 (7-8) ◽  
pp. 607-610 ◽  
Author(s):  
Christian Karl ◽  
Peter Alsted Pedersen ◽  
Gerhard Müller
Keyword(s):  
Spectroscopic Methods ◽  
Aerial Parts ◽  
Acetone Extracts

Abstract Dryopteris filix-mas (L.) Schott, Polypodiaceae, Flavan, Dihydrocoumarin, Lactone From acetone extracts of fresh aerial parts of Dryopteris filix-mas (L.) Schott a flavan-3-ol was isolated. Its structure was elucidated as 5-(3,4-dihydroxyphenyl)-3,3a,4,5-tetrahydro-4,8-dihydro-xy-2H-pyrano[4,3,2-ife]-l-benzopyran-2-one by means of spectroscopic methods including l3C-NMR.

scholarly journals New Guaianolide-Type Sesquiterpene Lactones from Inula verbascifolia

2013 ◽  
Vol 68 (5-6) ◽  
pp. 175-180
Author(s):  
Abou El-Hamd H. Mohamed ◽  
Hosam-Eldin H. Mahmoud ◽  
Fathy F. Abdellatif ◽  
Yousif S. Mohamed ◽  
Ahmed A. Ahmed
Keyword(s):  
Sesquiterpene Lactones ◽  
Spectroscopic Methods ◽  
H Nmr ◽  
Aerial Parts ◽  
C Nmr

The aerial parts of Inula verbascifolia afforded two new guaianolide-type sesquiterpene lactones. Their structures were determined by spectroscopic methods (IR, MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, HMQC, and HMBC).

scholarly journals Isoflavonoids from Desmodium heterophyllum Aerial Parts

2018 ◽  
Vol 13 (6) ◽  
pp. 1934578X1801300 ◽  
Author(s):  
Le Minh Ha ◽  
Nguyen Thi Luyen ◽  
Ngo Thi Phuong ◽  
Do Thi Thanh Huyen ◽  
Le Mai Huong ◽  
...  
Keyword(s):  
Digestive Enzymes ◽  
Spectroscopic Methods ◽  
Inhibitory Effects ◽  
Aerial Parts

Five isoflavanoids including one new, (3 R)–2′,4′,5,7-tetrahydroxy-6-methylisoflavanone (1), were isolated from the aerial parts of Desmodium heterophyllum. Their structures were elucidated using spectroscopic methods. Their inhibitory effects on digestive enzymes α-glucosidase and α-amylase were evaluated. Genistein (5) and dalbergioidin (2) inhibited both enzymes. Their IC50 values were found at 110.4 and 162.8 μM for α-amylase, and at 257.3 and 412.6 μM for α-glucosidase, respectively.

scholarly journals Four New ent-Kaurane Diterpene Glycosides from Isodon henryi

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2736 ◽  
Author(s):  
Liu ◽  
Zhang ◽  
Wu ◽  
Chen ◽  
Li ◽  
...  
Keyword(s):  
Cell Lines ◽  
Human Cancer ◽  
Spectroscopic Methods ◽  
Human Cancer Cell ◽  
Human Cancer Cell Lines ◽  
Aerial Parts ◽  
Ic50 Values ◽  
Hct 116 ◽  
Relationship Of ◽  
First Time

To obtain diterpene glycosides from an aqueous extract of the aerial parts of Isodon henryi and further investigate their cytotoxicities, in this study, a total of seven compounds were isolated, including six ent-kaurane diterpene glycosides (1–6) and one diterpene aglycon (7). Among the seven ent-kaurane diterpenes obtained, four were novel compounds, including ent-7,20-epoxy- kaur-16-en-1α,6β,7β,15β-tetrahydroxyl-11-O-β-d-glucopyranoside (1), ent-7,20-epoxy-kaur-16-en- 6β,7β,14β,15β-tetrahydroxyl-1-O-β-d-glucopyranoside (2), ent-7,20-epoxy-kaur-16-en-6β,7β,15β- trihydroxyl-1-O-β-d-glucopyranoside (3), and ent-7,20-epoxy-kaur-16-en-7β,11β,14α,15β-tetrahydr- oxyl-6-O-β-d-glucopyranoside (4), and three were isolated from this plant for the first time (5–7). Their structures were elucidated by utilizing spectroscopic methods and electronic circular dichroism analyses. Furthermore, the cytotoxicities of all seven compounds were investigated in four human cancer cell lines, including A2780, BGC-823, HCT-116, and HepG2. The IC50 values of these diterpenes ranged from 0.18 to 2.44 mM in the tested cell lines. In addition, the structure–cytotoxicity relationship of diterpene glycosides was also evaluated to study the effect of glycosylation on the cytotoxicity of diterpene compounds.

Dammarane triterpenoid saponins from Bacopa monnieri

2009 ◽  
Vol 87 (9) ◽  
pp. 1230-1234 ◽  
Author(s):  
Pamita Bhandari ◽  
Neeraj Kumar ◽  
Bikram Singh ◽  
Inderjeet Kaur
Keyword(s):  
Medicinal Plant ◽  
2D Nmr ◽  
Bacopa Monnieri ◽  
Spectroscopic Methods ◽  
Triterpenoid Saponins ◽  
Enhancing Effect ◽  
Indian Medicinal Plant ◽  
Aerial Parts ◽  
Memory Enhancer ◽  
Memory Enhancing

Bacopa monnieri is a well-known Ayurvedic Indian medicinal plant traditionally used as a memory enhancer. Its memory-enhancing effect is mainly attributed to dammarane triterpenoid saponins. In the present study, two new dammarane-type triterpenoid saponins, bacopaside-XI (1) and bacopaside-XII (2), together with known compounds, bacopaside IV, bacopaside V, and apigenin, were isolated from the aerial parts of the B. monnieri . The structures of the new saponins were elucidated as 3-O-[α-L-arabinofuranosyl(1→3)]-6-O-sulfonyl-β-D-glucopyranosyl pseudojujubogenin (1) and 3-O-{β-D-glucopyranosyl(1→3)[α-L-arabinofuranosyl(1→2)]-β-D-glucopyranosyl}-20-O-α-L-arabinopyranosyl pseudojujubogenin (2) on the basis of extensive investigations of 1D and 2D NMR (HMQC and HMBC), ESI-QTOF-MS/MS spectroscopic methods, and chemical evidences.

Flavonoids from Tephrosia major. A New Prenyl-β-hydroxychalcone

2002 ◽  
Vol 57 (7-8) ◽  
pp. 579-583 ◽  
Author(s):  
Federico Gómez-Garibay ◽  
Oswaldo Téllez-Valdez ◽  
Gregorio Moreno-Torres ◽  
José S. Calderón
Keyword(s):  
2D Nmr ◽  
Spectroscopic Methods ◽  
Prenylated Flavonoids ◽  
Aerial Parts

The roots and aerial parts of Tephrosia major Micheli, afforded a new prenylated-β-hydroxychalcone, characterized as 2′,6′-dihydroxy-3′-prenyl-4′-methoxy-β-hydroxychalcone. In addition, seven prenylated flavonoids, two rotenoids, β-sitosterol, stigmasterol, lupeol and quercetin were isolated. The structure of the new β-hydroxy chalcone was established by spectroscopic methods, including 2D NMR experiments.

scholarly journals Phytochemical study of aerial parts from Phlomis tuberosa L

2014 ◽  
Vol 14 ◽  
pp. 20-24 ◽  
Author(s):  
S Javzan ◽  
D Selenge
Keyword(s):  
Carboxylic Acid ◽  
Methyl Ester ◽  
1H Nmr ◽  
Column Chromatography ◽  
Methanol Extract ◽  
Iridoid Glycoside ◽  
Chloroform Fraction ◽  
Spectroscopic Methods ◽  
Phytochemical Study ◽  
Aerial Parts

Three iridoid glycoside lamiide(I), Ipolamiide(II) and ipolamiide(III) were isolated from N-butanol fractions obtained from the column chromatography of methanol extract from the aerial parts of Phlomis tuberosa. In addition, iridoid cyclopenta[c]pyran-4-carboxylic acid, 7-methyl-, methyl ester and phenol, 4-(3-hydroxy-1-propenyl)-2-methoxy were determined from the chloroform fraction of methanol extract of aerial parts from Phlomis tuberosa. Isolation and structural elucidation of compounds were accomplished by PTLC, TLC, CC and spectroscopic methods (UV, 13C and 1H NMR and DEPT, GC-MS). DOI: http://dx.doi.org/10.5564/mjc.v14i0.192 Mongolian Journal of Chemistry 14 (40), 2013, p20-24

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