Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Priti Adlakha"'
Autor:
M. A. Sridhar, S. Naveen, Atul Manvar, S. Lakshmi, Anamik Shah, Priti Adlakha, Denish Karia, J. Shashidhara Prasad
Publikováno v:
Journal of Chemical Crystallography. 39:389-394
A novel unsymmetrical dihydropyridine, possessing carboxymethyl and carbomethoxy groups at C(3) and C(5), respectively, has been produced using a modified Hantzsch synthesis, under solvent free conditions, in a domestic microwave oven. The product ob
Autor:
Priti Adlakha, S. Naveen, M. A. Sridhar, Anamik Shah, J. Shashidhara Prasad, Chintan Dholakia
Publikováno v:
Structural Chemistry. 17:569-575
A novel dihydropyrimidine (DHPM) derivative bearing a carbamoyl moiety was synthesized by an efficient three-component Biginelli reaction and was characterized spectroscopically and finally confirmed by X-ray diffraction studies. The title compound C
Autor:
Manisha Parmar, Kuldip Upadhyay, Shrey Parekh, Priti Adlakha, Hardevsinh Vala, Shailesh Thakrar, Dhairya Bhavsar, Ashish Radadiya, Anamik Shah, Mahesh M. Savant, Abhay Bavishi
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(8)
A series of 4-styrylcoumarin have been synthesized by Knoevenagel condensation between substituted 4-methylcoumarin-3-carbonitrile and different heterocyclic or aromatic aldehydes. 4-Methylcoumarin-3-carbonitrile has been synthesized by the base cata
Autor:
Chintan Dholakia, Anamik Shah, Raghuvir R. S. Pissurlenkar, Evans C. Coutinho, Dinesh Manvar, Priti Adlakha, Vijay Virsodia
Publikováno v:
European journal of medicinal chemistry. 43(10)
Multi-drug resistance to commonly used antitubercular drugs has propelled the development of new structural classes of antitubercular agents. This paper reports the synthesis, evaluation and 3D-QSAR analysis of a set of substituted N-phenyl-6-methyl-
Autor:
Helga, Engi, Hiroshi, Sakagami, Masami, Kawase, Alpesh, Parecha, Dinesh, Manvar, Himanshu, Kothari, Priti, Adlakha, Anamik, Shah, Noboru, Motohashi, Imre, Ocsovszki, Joseph, Molnár
Publikováno v:
In vivo (Athens, Greece). 20(5)
The ability of 41 1,4-diphenyl-1,4-dihydropyridine derivatives to inhibit the transport activity of P-glycoprotein were studied by flow cytometry in a multidrug-resistant human colon cancer cell line (COLO320) and in human mdr1 gene-transfected mouse
Autor:
Sridhar M. Anandalwar, Beeranahally H. Doreswamy, Madegowda Mahendra, Anamik Shah, Kena Raval, J. Shashidhara Prasad, Priti Adlakha
Publikováno v:
Analytical Sciences: X-ray Structure Analysis Online. 21:X35-X36
The title compd. crystallizes in orthorhombic space group Pbca with a 13.9570(14), b 16.3850(9), c 16.6910(16) A�; Z = 8; R = 0.0560 for 2131 reflections. The 1,4-dihydropyridine (1,4-DHP) ring has a flat boat conformation. The mols. are linked int
Autor:
Bharat Varu, Beeranahally H. Doreswamy, Javaregowda S. Prasad, Madegowda Mahendra, Anamik Shah, Kena Raval, M. A. Sridhar, Priti Adlakha
Publikováno v:
Analytical Sciences: X-ray Structure Analysis Online. 19:X55-X56
The title compound was synthesized by the Hantzch method and characterized by the X-ray diffraction method. It crystallizes in monoclinic space group P21/c with cell parameters a = 8.722(7)A, b = 11.420(1)A, c = 13.307(1)A and Z = 4. The structure ha
Autor:
Priti Adlakha, S. Naveen, S. Lakshmi, Atul Manvar, Denish Karia, Anamik Shah, M. Sridhar, J. Shashidhara Prasad
Publikováno v:
Journal of Chemical Crystallography; Jun2009, Vol. 39 Issue 6, p389-394, 6p
Autor:
Kuldip Upadhyay, Sridhar M. Anandalwar, Anamik Shah, J. Shashidhara Prasad, Priti Adlakha, S. Naveen
Publikováno v:
Scopus-Elsevier
3-Nitro-4-hydroxycoumarin has been synthesized and characterized by X-ray diffraction analysis. The compound crystallizes in the orthorhombic crystal class in the space group Pc21b with cell parameters a = 18.5990(3)A, b = 5.0250(10)A, c = 8.871(2)A,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e09fe333d296a0165d316cba0c958a35
http://www.scopus.com/inward/record.url?eid=2-s2.0-70450237381&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-70450237381&partnerID=MN8TOARS