Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Dhilli Rao Gorja"'
Autor:
Fanxiang Yin, Ran Zhao, Dhilli Rao Gorja, Xiaorong Fu, Ning Lu, Hai Huang, Beibei Xu, Hanyong Chen, Jung-Hyun Shim, Kangdong Liu, Zhi Li, Kyle Vaughn Laster, Zigang Dong, Mee-Hyun Lee
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 12, Iss 11, Pp 4122-4137 (2022)
Colorectal cancer (CRC) is the second most common cause of cancer-related death in the world. The pro-viral integration site for Moloney murine leukemia virus 1 (PIM1) is a proto-oncogene and belongs to the serine/threonine kinase family, which are i
Externí odkaz:
https://doaj.org/article/5e196dc1029c489b8bc9f8c40f5aa4d5
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 338-345 (2011)
The Pd/C–CuI–PPh3 catalytic system facilitated C–C bond formation between 4-chlorothieno[2,3-d]pyrimidines and terminal alkynes in methanol with high selectivity without generating any significant side products arising from C–O bond formation
Externí odkaz:
https://doaj.org/article/ff2bbfc11bfc44308cc533e6de8b0667
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 64 (2009)
Pd/C-mediated alkynylation of 5-iodo-pyrazole-4-carboxylic acid, involving the first regioselective construction of α-pyrone ring on a pyrazol moiety via tandem coupling–cyclization process, has been developed to afford pyrano[4,3-c]pyrazol-4(1H)-
Externí odkaz:
https://doaj.org/article/03f059c4acf1450e8e6c650a0f60ab06
Autor:
Ravikumar Kapavarapu, Mandava Venkata Basaveswara Rao, A. V. D. Nagendra Kumar, Dhilli Rao Gorja, Bodapati Veera Durga Rao, Manojit Pal, Suryadevara V Vardhini
Publikováno v:
ChemistrySelect. 6:788-797
Autor:
Kangdong Liu, Fangfang Liu, Zhenjiang Zhao, H. S. Chen, Ann M. Bode, Zigang Dong, Guoguo Jin, Zhiping Guo, Keke Wang, Dhilli Rao Gorja, Ke Yao, Kanamata Reddy
Publikováno v:
Mol Carcinog
Osteosarcoma is the primary human malignant tumor affecting bone. This cancer most frequently arises in children and adolescents, with a second peak in those over the age of 50. Currently, surgery followed by radiotherapy and chemotherapy are the mai
Autor:
Ann M. Bode, H. S. Chen, Fangfang Liu, Guoguo Jin, Kanamata Reddy, Zigang Dong, Zhiping Guo, Kangdong Liu, Dhilli Rao Gorja, Ziming Dong, Ke Yao, Zhenjiang Zhao
Publikováno v:
Oncotarget
// Guoguo Jin 1, 2, 3 * , Ke Yao 1, 3, * , Zhiping Guo 1, 4, * , Zhenjiang Zhao 1, 4, * , Kangdong Liu 1, 2, 3 , Fangfang Liu 3 , Hanyong Chen 1 , Dhilli Rao Gorja 3 , Kanamata Reddy 1 , Ann M. Bode 1 , Ziming Dong 2 and Zigang Dong 1, 3 1 The Hormel
Autor:
Zigang Dong, Dhilli Rao Gorja, H. S. Chen, Ann M. Bode, Guoguo Jin, Ke Yao, Zhenjiang Zhao, Fangfang Liu, Kanamata Reddy, Zhiping Guo, Keke Wang, Kangdong Liu
Publikováno v:
SSRN Electronic Journal.
Osteosarcoma is the primary human malignant tumor affecting bone. This cancer most frequently arises in children and adolescents, with a second peak in those over the age of 50. Currently, surgery followed by radiotherapy and chemotherapy are the mai
Publikováno v:
Journal of Biomolecular NMR. 62:233-238
The S100 proteins constitute the largest family within the EF-hand protein superfamily, shown to bind and control various proteins involved in several cellular functions such as proliferation, differentiation, apoptosis, Ca homeostasis, and energy me
Autor:
Yinggao Meng, Chuanjun Song, Yuanyuan Xiao, Dhilli Rao Gorja, Qinghua Yang, Panpan Chen, Junbiao Chang, Jie Wu
Publikováno v:
RSC Advances. 5:79906-79914
An unprecedented Ag2CO3 and DBU mediated cyclization of 3-substituted 2-(2-bromoallyl)-3-oxo-1-carboxylates leading to the formation of 2,5-disubstituted furan-3-carboxylates has been reported. In the absence of a silver salt, the isomeric 2,4-disubs
Autor:
Sunder Kumar Kolli, Dhilli Rao Gorja, Girdhar Singh Deora, P. Vijaya Babu, K. Mukkanti, Chandana Lakshmi T. Meda, Manojit Pal, Kishore V. L. Parsa
Publikováno v:
Tetrahedron Letters. 55:3176-3180
The linkage between dopamine D2 receptors and PDE activity via cAMP prompted us to design a series of novel N-(3-arylprop-2-ynyl)substituted olanzapine derivatives as potential inhibitors of PDE4B. The target compounds were conveniently prepared by u