نتایج جستجو برای: benzopyran

تعداد نتایج: 614  

2009
R. Ravi Kumar M. Krishnaiah N. Jagadesh Kumar D. Gunasekhar Reddy V. G. Puranik

In the title compound, C(18)H(16)O(6), the dimethoxy-phenyl ring is rotated by 61.8 (1)° from the plane of the benzopyran system. The mol-ecule is stabilized by an intra-molecular O-H⋯O hydrogen bond.

Journal: :The Biochemical journal 1964
F H Stodola C Cabot C R Benjamin

Brewer (1958) described the isolation ofa number of fungi from slime samples taken from pulp and paper mills in Eastern Canada, one of the organisms being identified as Truncatella ramulosa (v. Beyma) Steyaert (Syn. Pestalotia ramulosa v. Beyma). In 1959, during a study of a subculture of this organism, we observed crystals in old cultures grown on malt-extract-agar. In a preliminary note Benja...

2008
Qiu-Ya Wang

The title compound, C(18)H(16)O(4), is composed of a benzopyran-one core with a 4-methoxy-phenyl subsituent in the 3-position and an additional eth-oxy group in the 7-position. The benzopyran-one ring is not coplanar with the benzene ring, the dihedral angle between them being 41.76 (7)°. The meth-oxy and eth-oxy substituents are nearly coplanar with the ring systems to which they are attached....

Journal: :Chemical and Pharmaceutical Bulletin 1987

2013
Ruchi Saxena Vishal Chandra Murli Manohar Kanchan Hajela Utsab Debnath Yenamandra S. Prabhakar Karan Singh Saini Rituraj Konwar Sandeep Kumar Kaling Megu Bal Gangadhar Roy Anila Dwivedi

Inhibition of epidermal growth factor receptor (EGFR) signaling is considered to be a promising treatment strategy for estrogen receptor (ER)-negative breast tumors. We have investigated here the anti-breast cancer properties of a novel anti-proliferative benzopyran compound namely, 2-[piperidinoethoxyphenyl]-3-phenyl-2H-benzo(b)pyran (CDRI-85/287) in ER- negative and EGFR- overexpressing breas...

Journal: :Molecules 2007
Yong Rok Lee Xue Wang Likai Xia

An efficient and concise total synthesis of naturally occurring pyranochalcones was achieved from readily available 2,4-dihydroxyacetophenone and 2,4-dihydroxy-6-methoxyacetophenone. The key steps in the synthetic strategy were ethylenediamine diacetate-catalyzed benzopyran formation and aldol reactions.

2011
G. Chitra Devi Sundari Bhaskaran G. Usha G. Murugan M. Bakthadoss

In the title compound, C(20)H(20)FNO(3), the pyrrolidine and benzopyran rings adopt half chair and twisted half chair conformations, respectively. The carboxyl-ate group is almost perpendicular to the pyran ring [89.4 (1)°].

Journal: :iranian journal of pharmaceutical research 0
afsaneh zonouzi school of chemistry, university college of science, university of tehran, p.o. box 14155-6455, tehran, iran roghieh mirzazadeh school of chemistry, university college of science, university of tehran, p.o. box 14155-6455, tehran, iran maliheh safavi institute of biochemistry and biophysics, department of biochemistry, university of tehran, tehran, iran sussan k ardestani institute of biochemistry and biophysics, department of biochemistry, university of tehran, tehran, iran saeed emami department of medicinal chemistry and pharmaceutical sciences research center, faculty of pharmacy, mazandaran university of medical sciences, sari, iran. alireza foroumadi 1- faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran. 2- drug design and development research center, tehran university of medical sciences, tehran, iran.

a series of 2-amino-4-(nitroalkyl)-4h-chromene-3-carbonitriles were synthesized by an efficient multicomponent reaction in aqueous media using dbu (1,8-diazabicyclo[5.4.0]undec-7-ene) as a catalyst at room temperature. mild condition, environment friendly procedure and excellent yields are the main advantages of this procedure. the cytotoxic activity of target compounds were evaluated against t...

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