Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Shobanbabu, Bommagani"'
Autor:
Zaineb A.F. Albayati, Narsimha R. Penthala, Shobanbabu Bommagani, Ginell R. Post, Mark S. Smeltzer, Peter A. Crooks
Publikováno v:
Toxicology Reports, Vol 8, Iss , Pp 359-364 (2021)
Previous studies have demonstrated that the bone targeting agent BT2-peg2 (BT2-minipeg2, 9), when conjugated to vancomycin and delivered systemically by intravenous (IV) or intraperitoneal (IP) injection accumulates in bone to a greater degree than v
Externí odkaz:
https://doaj.org/article/b6e349550dab45d99adf22a3c3116c46
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 11, Pp 1543-1546 (2018)
The title compound, C21H25NO3 [systematic name: (1aR,4E,7aS,8E,10aS,10bR)-8-(2-aminobenzylidene)-1a,5-dimethyl-2,3,6,7,7a,8,10a,10b-octahydrooxireno[2′,3′:9,10]cyclodeca[1,2-b]furan-9(1aH)-one], was synthesized by the reaction of parthenolide [sy
Externí odkaz:
https://doaj.org/article/42d231684a0b454783d4456f270d1cb8
Publikováno v:
ARKIVOC, Vol 2017, Iss 4, Pp 20-33 (2017)
Externí odkaz:
https://doaj.org/article/22a19e115dbd4700bdd2d5b8e6f3eda1
Autor:
John P Moore II, Soma Shekar Dachavaram, Shobanbabu Bommagani, Narsimha Reddy Penthala, Priya Venkatraman, E. Johan Foster, Peter A. Crooks, Jamie A. Hestekin
Publikováno v:
Molecules, Vol 25, Iss 8, p 1847 (2020)
The 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) oxidation of cellulose, when mediated with Oxone® (KHSO5), can be performed simply and under mild conditions. Furthermore, the products of the reaction can be isolated into two major components: Oxone
Externí odkaz:
https://doaj.org/article/04326525d9204d5399abb1b5ee7037b3
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 12, Pp 1536-1538 (2015)
The title compound, C19H22N2O3, {systematic name (1aR,4E,7aS,8E,10aS,10bR)-1a,5-dimethyl-8-[(pyrimidin-5-yl)methylidene]-2,3,6,7,7a,8,10a,10b-octahydrooxireno[2′,3′:9,10]cyclodeca[1,2-b]furan-9(1aH)-one} was obtained from the reaction of partheno
Externí odkaz:
https://doaj.org/article/cee554514b3b4b42828d9834b588cdfc
Autor:
Narsimha Reddy Penthala, Nikhil Reddy Madadi, Shobanbabu Bommagani, Sean Parkin, Peter A. Crooks
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 11, Pp 392-395 (2014)
The title compound, C19H17N3O3S (I), was prepared by a [3 + 2]cycloaddition azide condensation reaction using sodium azide and l-proline as a Lewis base catalyst. N-Methylation of compound (I) using CH3I gave compound (II), C20H19N3O3S. The benzothio
Externí odkaz:
https://doaj.org/article/ce281d44e6794c01830abda69376dfc7
Autor:
Narsimha Reddy Penthala, Peter A. Crooks, Mark S. Smeltzer, Ginell R. Post, Shobanbabu Bommagani, Zaineb A.F. Albayati
Publikováno v:
Toxicology Reports
Toxicology Reports, Vol 8, Iss, Pp 359-364 (2021)
Toxicology Reports, Vol 8, Iss, Pp 359-364 (2021)
Graphical abstract
Previous studies have demonstrated that the bone targeting agent BT2-peg2 (BT2-minipeg2, 9), when conjugated to vancomycin and delivered systemically by intravenous (IV) or intraperitoneal (IP) injection accumulates in bone to
Previous studies have demonstrated that the bone targeting agent BT2-peg2 (BT2-minipeg2, 9), when conjugated to vancomycin and delivered systemically by intravenous (IV) or intraperitoneal (IP) injection accumulates in bone to
Autor:
Linda P. Dwoskin, Satheesh Gujarathi, Na-Ra Lee, Kiranbabu Siripurapu, Shobanbabu Bommagani, Guangrong Zheng
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:471-476
Novel quinuclidinyl N-phenylcarbamate analogs were synthesized, and binding affinities at M1-M5 muscarinic acetylcholine receptor (mAChR) subtypes were determined using Chinese hamster ovary (CHO) cell membranes stably expressing one specific subtype
Autor:
Ramesh Balusu, Monica L. Guzman, Peter A. Crooks, Narsimha Reddy Penthala, Shobanbabu Bommagani, Meenakshisundaram Balasubramaniam, Sudhakiranmayi Kuravi, Eloisi Caldas-Lopes
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:172-178
A series of novel tetrazole analogues of resveratrol were synthesized and evaluated for their antileukemic activity against an extensive panel of human cancer cell lines and against the MV4-11 AML cell line. These molecules were designed as drug-like
Autor:
Nikhil Reddy Madadi, Narsimha Reddy Penthala, Shobanbabu Bommagani, Sean Parkin, Peter A. Crooks
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 10, Pp o1128-o1129 (2014)
The title compound, C20H23N3O6·CH3OH, was synthesized by [3 + 2] cycloaddition of (Z)-2,3-bis(3,4,5-trimethoxyphenyl)acrylonitrile with sodium azide and ammonium chloride in DMF/water. The central nitrogen of the triazole ring is protonated. The dih
Externí odkaz:
https://doaj.org/article/f39f8ce9d1fd46b885c73d0a002c719b