scholarly journals A Novel C21 Cyclopentenone Derivative from Cipadessa Cinerascens

2015 ◽  
Vol 10 (8) ◽  
pp. 1934578X1501000
Author(s):  
Jing Zhang ◽  
Yao-Wen Chang ◽  
Chun-Mao Yuan ◽  
Fan Zhang ◽  
Ying-Tong Di ◽  
...  
Keyword(s):  
Cell Lines ◽  
Spectroscopic Analysis ◽  
2D Nmr ◽  
Cytotoxicity Activity ◽  
Nmr Techniques

A new C21 cyclopentenone derivative, Cipacyclonone (1), was isolated from the leaves of Cipadessa cinerascens. Its structure was elucidated on the basis of spectroscopic analysis, including extensive 1D- and 2D-NMR techniques. Compound 1 showed strong cytotoxicity activity against HL-60 and A-549 cell lines, with IC50 values of 1.2 and 3.0 μM, respectively.

Isolation of New Glycosides from Anemarrhena Asphodeloides Rhizome and Screening of their Anticancer Activity

2019 ◽  
Vol 16 (6) ◽  
pp. 474-477 ◽  
Author(s):  
Pham Van Khang ◽  
Nguyen Thi Hien Lan ◽  
Le Quang Truong ◽  
Mai Thi Minh Chau ◽  
Mai Xuan Truong ◽  
...  
Keyword(s):  
Anticancer Activity ◽  
Spectral Data ◽  
Cell Lines ◽  
Cancer Cell ◽  
Spectroscopic Analysis ◽  
2D Nmr ◽  
Ic50 Values ◽  
Nmr Techniques ◽  
Inhibitory Activities ◽  
Anemarrhena Asphodeloides

In this report, two new steroidal glycosides were isolated and determined from n-butanol fraction of A.asphodeloides. The structures were confirmed in comparison with the spectral data of known compounds by using different spectroscopic analysis approaches including 1D & 2D-NMR techniques and HRMS. The anti-proliferation screening against cancer cell lines A549 and HeLa indicated that compound 1 exhibited good inhibitory activities with IC50 values of 0.79 and 0.55 µg/mL, respectively.

scholarly journals Chemical Constituents of Cordyceps cicadae

2015 ◽  
Vol 10 (12) ◽  
pp. 1934578X1501001 ◽  
Author(s):  
Zhi-Bo Chu ◽  
Jun Chang ◽  
Ying Zhu ◽  
Xun Sun
Keyword(s):  
Amino Acids ◽  
Spectroscopic Analysis ◽  
Chemical Constituents ◽  
2D Nmr ◽  
Cordyceps Cicadae ◽  
Nmr Techniques ◽  
Dopamine Analogues

One new bifuran derivative (1), together with fourteen known compounds, were isolated from Cordyceps cicadae X. Q. Shing. The known compounds included nine nucleosides, uracil (2), uridine (3), 2′-deoxyuridine (4), 2′-deoxyinosine (5), guanosine (6), 2′-deoxyguanosine (7), thymidine (8), adenosine (9), and 2′-deoxyadenosine (10); three amino acids tryptophan (11), phenylalanine (12), and tyrosine (13); and two dopamine analogues N-acetylnoradrenaline (14) and its dimer, trans–2-(3′,4′-dihydroxyphenyl)-3-acetylamino-7-( N-acetyl-2″-amino-ethylene)-1,4-benzodioxane (15). Their structures were decisively elucidated by spectroscopic analysis, including 1D and 2D NMR techniques.

scholarly journals Synthesis and Anti-Proliferative Assessment of Triazolo-Thiadiazepine and Triazolo-Thiadiazine Scaffolds

Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4471 ◽  
Author(s):  
Ahmed T. A. Boraei ◽  
Hazem A. Ghabbour ◽  
Mohamed S. Gomaa ◽  
El Sayed H. El Ashry ◽  
Assem Barakat
Keyword(s):  
Single Crystal ◽  
Cell Lines ◽  
Cancer Cell ◽  
2D Nmr ◽  
Cancer Cell Lines ◽  
Docking Studies ◽  
X Ray ◽  
Cytotoxicity Activity ◽  
Human Liver Cancer ◽  
Mcf 7

A series of triazolo-thiadiazepines 4a–k were synthesized with excellent yields using dehydrated PTSA as a catalyst in toluene. Two triazolo-thiadiazines were obtained; 8a was formed directly by reflux in ethanol, whereas, PTSA promoted the formation of 8b. The molecular structure of the formed triazolo-thiadiazepines is identical to the imine-form 4a–k and not the enamine-tautomer 6a–k. The structures of the newly synthesized triazolo-thiadiazepines 4a–k and triazolo-thiadiazines 8a–b were elucidated using NMR (1H, and 13C), 2D NMR, HRMS, and X-ray single crystal. Furthermore, 4a was deduced using X-ray single crystal diffraction analysis. These new thiadiazepine hits represent an optimized series of previously synthesized indole-triazole derivatives for the inhibition of EGFR. The cytotoxicity activity against two cancer cell lines including human liver cancer (HEPG-2) and breast cancer (MCF-7) was promising, with IC50 between 12.9 to 44.6 µg/mL and 14.7 to 48.7 µg/mL for the tested cancer cell lines respectively, compared to doxorubicin (IC50 4.0 µg/mL). Docking studies revealed that the thiadiazepine scaffold presented a suitable anchor, allowing good interaction of the various binding groups with the enzyme binding regions and sub-pockets.

scholarly journals A Novel Phenolic Compound from Phyllanthus emblica

2013 ◽  
Vol 8 (4) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Gaimei She ◽  
Ruiyang Cheng ◽  
Lei Sha ◽  
Yixia Xu ◽  
Renbin Shi ◽  
...  
Keyword(s):  
Phenolic Compound ◽  
Spectroscopic Analysis ◽  
2D Nmr ◽  
Phyllanthus Emblica ◽  
Mucic Acid ◽  
Nmr Techniques

A new compound, mucic acid 3- O-gallate (1), was isolated from the fruit of Phyllanthus emblica L, together with 5 known compounds (2-6). Their structures were elucidated on the basis of spectroscopic analysis, including 1D and 2D NMR techniques, and by comparison with literature data.

scholarly journals β-Elemene derivatives produced from SeO 2 -mediated oxidation reaction

2020 ◽  
Vol 7 (5) ◽  
pp. 200038
Author(s):  
Xingrui He ◽  
Xiao-Tao Zhuo ◽  
Yuan Gao ◽  
Renren Bai ◽  
Xiang-Yang Ye ◽  
...  
Keyword(s):  
Cell Lines ◽  
Cancer Cell ◽  
Oxidation Reaction ◽  
2D Nmr ◽  
Single Step ◽  
Easy Access ◽  
Nmr Techniques ◽  
One Step ◽  
New Compounds ◽  
Mediated Oxidation

Herein, we report the first access of β-elemene derivatives through the SeO 2 -mediated oxidation reaction. Several new compounds were isolated through such a one-step reaction, and their structures were elucidated using various 2D-NMR techniques. This method provides easy access to multiple oxidative β-elemene derivatives in one single step and represents the first modifications on cyclohexyl ring of β-elemene. It is expected to open up the opportunity for future derivatization on cyclohexyl ring of β-elemene. The new compounds obtained above showed better anti-proliferation activities than β-elemene itself on several cancer cell lines. Among them, compound 17 shows the best activity in antiproliferation assays of A549 and U-87MG cell lines.

MWL fraction with a high concentration of lignin-carbohydrate linkages: Isolation and 2D NMR spectroscopic analysis

Holzforschung ◽  
2007 ◽  
Vol 61 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Mikhail Yu. Balakshin ◽  
Ewellyn A. Capanema ◽  
Hou-min Chang
Keyword(s):  
Loblolly Pine ◽  
Spectroscopic Analysis ◽  
Direct Detection ◽  
2D Nmr ◽  
Side Chain ◽  
High Concentration ◽  
Hmbc Correlation ◽  
Nmr Techniques ◽  
C Nmr ◽  
Hmbc Technique

Abstract A preparation enriched in lignin-carbohydrate fragments (LCC-AcOH) was isolated in the course of purification of loblolly pine crude milled wood lignin (MWL). The preparation contained approximately equal amounts of lignin and carbohydrates, with high amounts of arabinose and galactose compared to their levels in wood. LCC-AcOH was investigated by 2D 1H-13C (HMQC and HMBC) correlation NMR techniques and quantitative 13C NMR. The HMQC spectra allowed direct detection of phenyl glycoside, ester and benzyl ether lignin-carbohydrates linkages in high amounts. The assignment of these structures was supported by the HMBC technique. It is noteworthy that in the ester lignin-carbohydrate linkages, a uronic acid residue was attached not to the benzylic position of lignin, as commonly believed, but to the γ-position of the side chain.

scholarly journals Synthesis and structure of (R,S)-2-methyl-4-(4-nitrophenyl)-pyrano[3,2-c]chromen-5(4H)-one

2012 ◽  
Vol 32 (2) ◽  
pp. 239
Author(s):  
Rosica P. Nikolova ◽  
Boris Shivachev ◽  
Bozhana Mikhova ◽  
Bistra Stamboliyska ◽  
Kristina Mladenovska ◽  
...  
Keyword(s):  
Spectroscopic Data ◽  
Chemical Structure ◽  
Spectroscopic Analysis ◽  
2D Nmr ◽  
The Novel ◽  
Phosphoryl Chloride ◽  
Torsion Angles ◽  
X Ray ◽  
Nmr Techniques ◽  
High Yields

In this paper, the synthesis and structure of a novel pyrano[3,2-c]coumarin, which was obtained unexpectedly in a reaction of phosphoryl chloride and acenocoumarol, are presented. The chemical structure of the novel compound was elucidated by a detailed spectroscopic analysis based mainly on 1D and 2D NMR techniques. The structure was finally confirmed with a single-crystal X-ray analysis. The B3LYP/6-311+G** method correctly reproduces the bond lengths, bond angles, torsion angles, and other experimental spectroscopic data, which can be useful for investigating the characteristics of some structurally related molecules. Additionally, the title compound was obtained in high yields by performing a dehydratation reaction of acenocuomarol with acetic anhydride.  

scholarly journals Isomeric Polycyclic Polyprenylated Acylphloroglucinols from the Bark of Mesua ferrea (Clusiaceae)

2017 ◽  
Vol 12 (8) ◽  
pp. 1934578X1701200
Author(s):  
Nurulfazlina Edayah Rasol ◽  
Humera Naz ◽  
Khalijah Awang ◽  
Mohamad Jemain Mohamad Ridhwan ◽  
Yap Ken Choy ◽  
...  
Keyword(s):  
Ethyl Acetate ◽  
Inhibitory Activity ◽  
Spectroscopic Analysis ◽  
Ethyl Acetate Extract ◽  
2D Nmr ◽  
Positive Control ◽  
Preparative Hplc ◽  
Nmr Techniques

Five new isomeric polycyclic polyprenylated acylphloroglucinols (PPAPs) named mesuaferroic acid A, B, C, E and F (1–5) were isolated from ethyl acetate extract of Mesua ferrea L. (Clusiaceae). The isomeric compounds were obtained after extensive chromatographic procedures mainly using preparative HPLC. Structures were established after detailed spectroscopic analysis mostly by 2D NMR techniques. Compounds 4 and 5 exhibited good α-glucosidase inhibitory activity with IC50 values of 0.43 and 0.60 mM, respectively, comparing to the positive control, 1-deoxynojirimycin (IC50 0.63 mM).

Xylogranatin E, a New Phragmalin with a Rare Oxygen Bridge between C1 and C29, from the Fruit of a Chinese Mangrove Xylocarpus granatum

2007 ◽  
Vol 62 (4) ◽  
pp. 569-572 ◽  
Author(s):  
Jun Wu ◽  
Haixin Ding ◽  
Minyi Li ◽  
Si Zhang
Keyword(s):  
Spectroscopic Analysis ◽  
2D Nmr ◽  
Oxygen Bridge ◽  
Nmr Data ◽  
Xylocarpus Granatum ◽  
Complete Assignment ◽  
Nmr Techniques ◽  
Noesy Spectra ◽  
C Nmr

Xylogranatin E, the second phragmalin with a rare oxygen bridge between C1 and C29 found in nature, was isolated from the fruit of a Chinese mangrove, Xylocarpus granatum. Its structure was determined by spectroscopic analysis. Complete assignment of 1H and 13C NMR data of xylogranatin E was achieved by 2D NMR techniques, including 1H-1H COSY, HSQC, HMBC and NOESY spectra.

scholarly journals A Novel Cycloartane Triterpenoid Bisdesmoside from Actaea vaginata

2017 ◽  
Vol 12 (10) ◽  
pp. 1934578X1701201
Author(s):  
Qiongyu Zou ◽  
Meichun Wu ◽  
Yindi Zhu ◽  
Jinping Shen ◽  
Guoxu Ma ◽  
...  
Keyword(s):  
Cell Lines ◽  
Cancer Cell ◽  
Spectroscopic Analysis ◽  
Ethanolic Extract ◽  
2D Nmr ◽  
Cancer Cell Lines ◽  
Cytotoxic Activities ◽  
Chemical Methods

A new cycloartane triterpenoid bisdesmoside, soulieoside S (1), was isolated from the ethanolic extract of rhizomes of Actaea vaginata. The structure was determined by extensive spectroscopic analysis including 1D- and 2D NMR and HRESIMS, as well as chemical methods. Compound 1 was evaluated for its cytotoxic activities against HepG2, MDA-MB231 and A549 cancer cell lines.

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