Synthesis and photochromic properties of oxime derivatives of 2,3-diarylcyclopent-2-en-1-ones

2013 ◽  
Vol 12 (9) ◽  
pp. 1717 ◽  
Author(s):  
Valerii Z. Shirinian ◽  
Dmitry V. Lonshakov ◽  
Andrey G. Lvov ◽  
Alexey A. Shimkin ◽  
Mikhail M. Krayushkin
1996 ◽  
Vol 61 (2) ◽  
pp. 288-297 ◽  
Author(s):  
Vladimír Pouzar ◽  
Ivan Černý

New approach to the preparation of steroids with connecting bridge, based on an O-carboxymethyloxime (CMO) structure, and with terminal hydroxy group, is presented. 17-CMO derivatives of 3β-acetoxy- and 3β-methoxymethoxyandrost-5-en-17-one were condensed with α,ω-amino alcohols to give derivatives with a chain of seven to nine atoms. After THP-protection, these compounds were converted to 3-keto-4-ene derivatives. An alternative synthesis consisted in transformation of 17-CMO derivatives with bonded amino acids by reduction of the terminal carboxyl. The resulting compounds were designed as building blocks for the preparation of bis-haptens for sandwich immunoassays.


Molecules ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 679 ◽  
Author(s):  
Joanna Kozłowska ◽  
Ewa Grela ◽  
Dagmara Baczyńska ◽  
Agnieszka Grabowiecka ◽  
Mirosław Anioł

In our investigation, we concentrated on naringenin (NG)—a widely studied flavanone that occurs in citrus fruits. As a result of a reaction with a range of alkyl iodides, 7 novel O-alkyl derivatives of naringenin (7a–11a, 13a, 17a) were obtained. Another chemical modification led to 9 oximes of O-alkyl naringenin derivatives (7b–13b, 16b–17b) that were never described before. The obtained compounds were evaluated for their potential antibacterial activity against Escherichia coli, Staphylococcus aureus, and Bacillus subtilis. The results were reported as the standard minimal inhibitory concentration (MIC) values and compared with naringenin and its known O-alkyl derivatives. Compounds 4a, 10a, 12a, 14a, 4b, 10b, 11b, and 14b were described with MIC of 25 µg/mL or lower. The strongest bacteriostatic activity was observed for 7-O-butylnaringenin (12a) against S. aureus (MIC = 6.25 µg/mL). Moreover, the antitumor effect of flavonoids was examined on human colon cancer cell line HT-29. Twenty-six compounds were characterized as possessing an antiproliferative activity stronger than that of naringenin. The replacement of the carbonyl group with an oxime moiety significantly increased the anticancer properties. The IC50 values below 5 µg/mL were demonstrated for four oxime derivatives (8b, 11b, 13b and 16b).


Lipids ◽  
2008 ◽  
Vol 43 (3) ◽  
pp. 275-280 ◽  
Author(s):  
Viral V. Brahmbhatt ◽  
Christopher Nold ◽  
Carolyn J. Albert ◽  
David A. Ford

1991 ◽  
Vol 55 (10) ◽  
pp. 2615-2621 ◽  
Author(s):  
Yoshihisa Tsukamoto ◽  
Kazuo Sato ◽  
Shigeru Mio ◽  
Soji Sugai ◽  
Toshiaki Yanai ◽  
...  

2011 ◽  
Vol 2 (3) ◽  
pp. 388-393 ◽  
Author(s):  
Ashutosh Barve ◽  
Malleshappa Noolvi ◽  
Niharika Subhedar ◽  
Vishnu Dev Gupta ◽  
Gaurav Bhatia

2009 ◽  
Vol 22 (5) ◽  
pp. 537-545 ◽  
Author(s):  
Evgeni M. Glebov ◽  
Artjom B. Smolentsev ◽  
Valeri V. Korolev ◽  
Victor F. Plyusnin ◽  
Anna V. Chebunkova ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document