scholarly journals CHEMICAL CONSTITUENTS FROM POLYGONATUM KINGIANUM COLL. ET HEMSL. OF VIETNAM

2020 ◽  
Vol 58 (5) ◽  
pp. 549
Author(s):  
Lê Minh Hà

Seven compounds, including two homoisoflavanones 3-(2ʹ-hydroxy-4ʹ-methoxy-benzyl)-5,7-dihydroxy-8-methyl-chroman-4-one (1), disporopsin (2) along with 2-O-methyl-α-D-fructofuranose (3), (E,E)-9-oxooctadeca-10,12-dienoic acid (4), 1-palmitoylglycerol (5), 5α,8α-ergosterol  peroxide (6),  daucosterol (7) were isolated from the rhizomes of Polygonatum kingianum of Vietnam. Their structures were determined by 1D and 2D NMR spectra and by comparison with the reported spectral data. Compounds 3, 4 and 6 are first reported from the genus Polygonatum. Compound 1 and 5 are reported for the first time from Polygonatum kingianum.

2009 ◽  
Vol 64 (3) ◽  
pp. 323-327 ◽  
Author(s):  
Tran Thi Phuong Thao ◽  
Nguyen Vu Anh ◽  
Ho Ngoc Anh ◽  
Tran Duc Quan ◽  
Tran Van Sung

A new bisabolene derivative (1S*, 2R*, 4R*, 7R*, 10R*)-1,7,10,11-tetrahydroxy-1,7,11-trimethyl- 4,10(H)-2-O-cinnamoyl-bisabol-8(9)-ene (1), together with cinnamic acid (2), methyl cinnamate (3), sodium cinnamate (4) and methyl elaidate (5) have been isolated from the leaves and barks of Fissistigma petelotii. Sodium cinnamate (4) was isolated for the first time from the nature. The structures of these compounds were elucidated by analysis of their IR, MS, 1D and 2D NMR spectra.


2019 ◽  
Vol 57 (1) ◽  
pp. 1
Author(s):  
Le Minh Ha ◽  
Ngo Thi Phuong ◽  
Do Thi Thanh Huyen ◽  
Duong Bich Ngoc ◽  
Nguyen Minh Nguyet ◽  
...  

From the ethyl acetate extract of the leaves of Desmodium gangeticum collected in Me Linh, Ha Noi, we isolated 5 compounds including luteolin (1), luteolin tetramethyl ether (2),  N,N-dimethyl tetradecane-1-amin (3), D-pinitol (4)  and stigmasterol (5). In which, luteolin (1) was isolated from Desmodium gangeticum for the first time, luteolin tetramethyl ether (2) and  N,N-dimethyl tetradecane-1-amin (3) were first isolated from genus Desmodium. Their structures were determined by 1D and 2D NMR spectra.


2021 ◽  
Vol 16 (2) ◽  
pp. 1934578X2199334
Author(s):  
Do Thi Trang ◽  
Bui Huu Tai ◽  
Dan Thuy Hang ◽  
Pham Hai Yen ◽  
Phan Thi Thanh Huong ◽  
...  

Seven compounds (1-7) were isolated from the marine sponge Aaptos aaptos living in the Vietnamese sea. Their structures were determined as 2 hours, 5 H,7 H,9 H-9 S-hydroxy-imidazo[1,5- α]pyridine-1,3-dione (1), 3-([9-methylhexadecyl]oxy)propane-1,2-diol 2, 2,3-dihydro-2,3-dioxoaaptamine (3), indol-3-aldehyde (4), methyl indole-3-carboxylate (5) 4-hydroxy-5-(indole-3-yl)−5-oxo-pentan-2-one (6), and thymidine (7) by extensive analysis of HR-ESI-MS, 1D, and 2D NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. In addition, the absolute configuration of 1 was determined from the experimental ECD spectrum and comparison of this with the theoretical ECD calculations using the TDDFT method. Compounds 1 and 2 were isolated from nature for the first time. Compound 3 induced cytotoxic activity against SK-LU-1, MCF-7, HepG2, and SK-Mel-2 cell lines with IC50 values of 41.27 ± 2.63, 40.70 ± 2.65, 34.31 ± 3.43, and 36.63 ± 1.40 µM, respectively.


2008 ◽  
Vol 3 (2) ◽  
pp. 1934578X0800300 ◽  
Author(s):  
Vouffo Bertin ◽  
Hidayat Hussain ◽  
Simeon F. Kouam ◽  
Etienne Dongo ◽  
Gennaro Pescitelli ◽  
...  

Four compounds were isolated from the stem bark of Antiaris africana. One of them, a γ-lactone named antialactone (1a), is reported for the first time as a natural product. The structures were determined by comprehensive analyses of their 1D and 2D NMR spectra and EI MS data. The absolute configuration of antialactone acetate (1b) was established by TDDFT CD calculations and comparison with measured CD spectra. The remaining three known compounds were identified, by comparing their spectroscopic data with those reported in the literature, as lichenxanthone, β-sitosterol, and betulinic acid.


2016 ◽  
Vol 88 (1) ◽  
pp. 29-33 ◽  
Author(s):  
Eleane M.C. de Souza ◽  
Ellon L. Da Silva ◽  
Andrey M.R. Marinho ◽  
Patrícia S.B. Marinho

The present work reports the isolation of eight compounds fromPestalotiopsis sp. EJC07 isolated as endophytic fromBauhinia guianensis, a tipical plant of the Amazon. The compounds (4S)-4,8-dihydroxy-1-tetralone (1), uracil (2), uridin (3), p-hydroxybenzoic acid (4), ergosterol (5), ergosterol peroxide (6), cerevisterol (7) and ducitol (8) were isolated by chromatographic procedures and identified by spectral methods of 1D and 2D NMR and MS. The compound 1 is being reported for the first time in the genusPestalotiopsis.


2018 ◽  
Vol 1 (T5) ◽  
pp. 167-171
Author(s):  
Tung Thanh Nguyen ◽  
Thuong Thi Nguyen ◽  
Phu Hoang Dang ◽  
Trong Nguyen Huu Phan ◽  
Nhan Trung Nguyen

There is no research on the chemical constituents investigation and bioactivity evaluation of Buchanania lucida Blume (Anacardiaceae). From the stems of Buchanania lucida collected at Dong Nai province, the ethyl acetate and n-butanol extracts were prepared. Four phenolic compounds: protocatechuic methyl ester (1), aloe-emodin (2), naringenin (3), and glucosyringic acid (4) were isolated from these extracts. The chemical structure of these compounds were elucidated by 1D and 2D NMR spectra and comparison with published data. These compounds were first reported in Buchanania lucida.


2018 ◽  
Vol 56 (2A) ◽  
pp. 99-103
Author(s):  
Le Minh Ha

From the methanol extract of the leaves of Desmodium gangeticum collected in Me Linh, Ha Noi, we isolated 5 compounds. In which, there are four glycosides including (6S,9R)-roseoside (1), kaempferol-3-O-rutinoside (nicotiflorin) (2),  quercetin-3-O-rutinoside (rutin) (3), β-sitosterol-3-O- β-D-glucopyranoside (4), and the other is protocatechuic acid (5). Kaempferol-3-O-rutinoside (2) was isolated from Desmodium gangeticum for the first time while (6S,9R)-roseoside (1) was isolated from the genus Desmodium for the first time. Their structures were determined by 1D and 2D NMR spectra.


2014 ◽  
Vol 9 (5) ◽  
pp. 1934578X1400900 ◽  
Author(s):  
Dya Fita Dibwe ◽  
Suresh Awale ◽  
Shigetoshi Kadota ◽  
Hiroyuki Morita ◽  
Yasuhiro Tezuka

Two new diphenylmethyl-substituted xanthones, named muchimangins K (1) and L (2), have been isolated from the roots of Securidaca longepedunculata (Polygalaceae) collected in the Democratic Republic of Congo. Their structures were established by analyses of the spectral data, including 2D NMR spectra, to be l,3,6,8-tetrahydroxy-2,5-dimethoxy-4-[l-(2,4,5-trimethoxyphenyl)-1-phenylmethyl]xanthone (1) and l,3,6-trihydroxy-4,7-dimethoxy-2-[l-(2,4,5-trimethoxyphenyl)-1-phenylmethyl]xanthone (2).


2018 ◽  
Vol 13 (12) ◽  
pp. 1934578X1801301
Author(s):  
Pham Thi Bich Hanh ◽  
Ngo Thi Phuong ◽  
Le Ngoc Hung ◽  
Nguyen Quoc Dat ◽  
Dang Minh Tri ◽  
...  
Keyword(s):  
2D Nmr ◽  
Esi Ms ◽  

A new flavonol glucoside, kaempferol 3- O-[2″,4″-di- O-acetyl-6″- O-( E- p-coumaroyl)]-β-D-glucopyranoside (namely crypsinoside A) (1), along with 7 known compounds 2 – 8 were isolated from the leaves of Crypsinus trilobus (Houtt.) Copel. (Polypodiaceae) for the first time. Their structures were elucidated on the basis of HR-ESI-MS, 1D and 2D NMR spectra.


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