NMR spectra of natural coumarin derivatives II. Furocoumarins

1971 ◽  
Vol 7 (5) ◽  
pp. 557-562 ◽  
Author(s):  
M. E. Perel'son ◽  
Yu. N. Sheinker ◽  
G. P. Syrova
1970 ◽  
Vol 6 (1) ◽  
pp. 5-11 ◽  
Author(s):  
M. E. Perel'son ◽  
Yu. N. Sheinker ◽  
G. P. Syrova ◽  
K. F. Turchin

1971 ◽  
Vol 7 (6) ◽  
pp. 692-699 ◽  
Author(s):  
M. E. Perel'son ◽  
Yu. N. Sheinker ◽  
A. A. Savina ◽  
G. P. Syrova

2007 ◽  
Vol 5 (1) ◽  
pp. 85-88 ◽  
Author(s):  
Stojadin Dekic ◽  
Vidoslav Dekic ◽  
Branimirka Vucic ◽  
Biljana Dekic ◽  
Milan Dekic

Reactions of 4-chloro-2-oxo-2H-chromene-3-carbonitrile (1) with 4-methylpyridin- 2-ylamine (2) and 6-methoxy-benzothiazol-2-ylamine (3) in acetonitrile containing a catalytic amount of triethylamine gave the new coumarin derivatives 7-imino-10-methyl-7H- 5-oxa-7a,12-diaza-benzo[a]anthracen-6-one (4) and 7-imino-10-methoxy-7H-5-oxa-12- thia-7a,13-diaza-indeno[1,2-b]phenanthren-6-one (5) in 52 and 39% yields, respectively. The novel compounds were subjected to acid hydrolysis giving the corresponding oxoderivatives 10-methyl-5-oxa-7a,12-diaza-benzo[a]anthracene-6,7-dione (6) and 10- methoxy-5-oxa-12-thia-7a,13-diaza-indeno[1,2-b]phenanthrene-6,7-dione (7) in 64 and 58% yields, respectively. The structural assignments of the synthesized compounds were based on elemental analyses, IR and proton NMR spectra. .


1979 ◽  
Vol 34 (7) ◽  
pp. 1010-1014 ◽  
Author(s):  
P. Rodighiero ◽  
A. Guiotto ◽  
P. Manzini

Abstract Synthesis of isoponcimarin, 7-(3'-methyl-2',3'-epoxy-butiloxy)-8-(3"-methyl-2"-oxobutyl) coumarin, a natural coumarin isolated from Poncirus trifoliata L., was obtained starting from acetyl osthenol. From the intermediate 7-acetoxy-8-(3'-methyl-2'-oxobutyl) coumarin, the coumarin derivatives isomeranzin and dihydrooroselone were also prepared


2014 ◽  
Vol 79 (11) ◽  
pp. 1405-1411 ◽  
Author(s):  
Selma Spirtovic-Halilovic ◽  
Mirsada Salihovic ◽  
Snezana Trifunovic ◽  
Suncica Roca ◽  
Elma Veljovic ◽  
...  

For some synthesized coumarin derivatives, 1H and 13C NMR isotropic chemical shifts and some other molecular properties were calculated using density functional theory. The calculations yield reliable results, that are in good correlation with experimental data. This is a good basis for the collaboration between experimentalists and quantum chemists.


1988 ◽  
Vol 24 (12) ◽  
pp. 1330-1333 ◽  
Author(s):  
L. M. Ryzhenko ◽  
V. I. Labunskaya ◽  
B. F. Ryzhenko ◽  
A. D. Shebaldova

Author(s):  
Mujeeb Samar ◽  
Singh Kuldeep ◽  
Yogi Bhoomika ◽  
Ansari Vaseem ◽  
Sinha Shweta

Background: : Tuberculosis (TB) is an acute or chronic infectious disease caused by several species of Myco-bacterium, collectively called as tubercle bacilli or Mycobacterium tuberculosis complex. Around 10 million people get sick with tuberculosis (TB) each year. TB is the second leading cause of deaths today after HIV/AIDS. A serious problem in the context of MDR-TB, is the extensively drug-resistant TB which is an im-portant reason for the restricted chemotherapy in TB. Therefore, there is a need to explore new antitubercular (anti-TB) agents. Coumarin is an oxygen-containing heterocyclic compound and can be widely found in many natural products, and many of them display diverse biological activities.The wide spectrum of activities of coumarin molecules have intrigued the scientists to explore the natural coumarins and their synthetic deriva-tives for their potential as anti-TB drugs. Objective: The objective of this review is to emphasize on important coumarin analogs with anti-TB activities and their structure-activity relationships (SAR) for designing better anti-TB agents. Method: Latest, authentic and published reports on various synthetic and natural coumarin derivatives and their anti-TB activities is being thoroughly studied and analyzed. The structural requirements of coumarins as anti-TB drugs have also been studied. Results : Collection and compilation of reports on various synthetic and natural coumarin derivatives and their anti-TB activities is being done. Conclusion: The study provides latest report on coumarin derivatives synthesized as anti-TB agent and wheth-er their activity depends on structural changes or not.


2018 ◽  
Vol 115 ◽  
pp. 305 ◽  
Author(s):  
C.B. Oosthuizen ◽  
N. Kishore ◽  
V. Kumar ◽  
A. Ohja ◽  
N. Lall

1971 ◽  
Vol 26 (2) ◽  
pp. 113-114 ◽  
Author(s):  
A. Zheleva ◽  
L. Bubeva-Ivanova ◽  
S. L. Spassov

Three new natural coumarin substances 1, 2 and 3 (derivatives of 2′,2′-dimethyl-3′,4′-dihydroxydihydropyrano-5′,6′:6,7-coumarin) were isolated from the roots and fruits of Peucedanum arenarium W.K.On the basis of the spectral data from UV, IR, and NMR spectra of coumarin 1, named peuarenarine, it was assumed, that, it is an ester of 2′,2′-dimethyl-3′,4′-dihydroxy-dihydropyrano-5′,6′:6,7-coumarin and of angelic and 2,3-epoxy-2-methylbutyric acids.


2021 ◽  
Vol 22 (21) ◽  
pp. 11420
Author(s):  
Ewelina Kozioł ◽  
Krzysztof Jóźwiak ◽  
Barbara Budzyńska ◽  
Peter A. M. de Witte ◽  
Daniëlle Copmans ◽  
...  

Coumarins are a well-known group of plant secondary metabolites with various pharmacological activities, including antiseizure activity. In the search for new antiseizure drugs (ASDs) to treat epilepsy, it is yet unclear which types of coumarins are particularly interesting as a systematic analysis has not been reported. The current study performed behavioral antiseizure activity screening of 18 different coumarin derivatives in the larval zebrafish pentylenetetrazole (PTZ) model using locomotor measurements. Activity was confirmed for seven compounds, which lowered seizure-like behavior as follows: oxypeucedanin 38%, oxypeucedanin hydrate 74%, notopterol 54%, nodakenetin 29%, hyuganin C 35%, daphnoretin 65%, and pimpinellin 60%. These coumarins, together with nodakenin, underwent further antiepileptiform analysis by local field potential recordings from the zebrafish opticum tectum (midbrain). All of them, except for nodakenetin, showed pronounced antiepileptiform activity, decreasing PTZ-induced elevation in power spectral density (PSD) by 83–89% for oxypeucedanin, oxypeucedanin hydrate, and notopterol, 77% for nodakenin, 26% for nodakenetin, 65% for hyuganin C, 88% for daphnoretin, and 81% for pimpinellin. These data demonstrate the potential of diverse coumarin scaffolds for ASD discovery. Finally, the structural differences between active and inactive coumarins were investigated in silico for oxypeucedanin hydrate and byacangelicin for their interaction with GABA-transaminase, a hypothetical target.


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