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Selected Publications (out of 70 publications in July 2008)
1.
Ahmadibeni, Y., Parang, K. Solid-supported diphosphitylating and
triphosphitylating reagents for nucleoside modification. Curr. Protoc.
Nucleic Acid Chem. (2008) Chapter 13:Unit13.8.
2. Ye, G.,
Tiwari, R., Parang K. Development of Src tyrosine kinase substrate binding
site inhibitors. Curr. Opin. Investig. Drugs (2008) 9,
605-613.
3.
Ahmadibeni, Y.,
Parang, K.,
Synthesis and evaluation of oligodeoxynucleotides containing
diphosphodiester internucleotide linkages.
Angew. Chem. Int. Ed. (2007)
46, 4739-4743.
4.
Ahmadibeni, Y.,
Parang, K.
Solid-phase synthesis of symmetrical 5’,5’-dinucleoside mono-, di-, tri-,
and tetraphosphodiesters. Org. Lett.
In press.
5.
Bhandari, R., Saiardi, A., Ahmadibeni, Y., Snowman, A. M., Resnick, A. C.,
Kristiansen, T. Z., Molina, H., Pandey, A., Werner, Jr. J. K., Juluri, K.
R., Xu, Y., Prestwich, G. D.,
Parang, K.,
Snyder, S. H.
Protein pyrophosphorylation by inosotl pyrophosphates is a posttranslational
event. Proc. Nat. Acad. Sci.
U.S.A. 2007,
104, 15305-15310.
6.
Chimalakonda,
C., Agarwal, H., Kumar, A.,
Parang, K.,
Mehvar, R.
Synthesis, analysis, in vitro characterization, and in vivo disposition of a lamivudine-dextran conjugate for selective antiviral delivery to the liver.
Bioconjugate Chem.
in press.
7.
Ye, G., Nam, N.
H., Saleh,
A., Kumar,
A., Sun,
G., Shenoy,
D.
B., Amiji, M. M.,
Parang,
K.
Cellular delivery of phosphopeptides with
tripodal peptide analogues. J. Med. Chem.
2007,
50, 3604-3617.
8.
Ahmadibeni, Y.,
Hanley, M., White, M., Ayrapetov, M., Lin, X., Sun, G.,
Parang, K.
Metal-binding properties of a dicysteine-containing motif in protein
tyrosine kinases. ChemBioChem,
2007,
8, 1592-1605.
9.
Kumar, A.,
Wang, Y., Lin, X., Sun, G.,
Parang, K.
Synthesis and evaluation of 3-phenylpyrazolopyrimidine-peptide conjugates as
Src tyrosine kinase inhibitors. ChemMedChem,
2007,
2, 1346-1360.
10.
Gu, X.,
Wang,
Y., Kumar,
A., Ye, G.,
Parang, K.,
Sun, G.
Design and evaluation of hydroxamate derivatives as metal-mediated
inhibitors of a protein tyrosine kinase. J.
Med. Chem. (2006)
49, 7532-7539.
11.
Kumar, A., Ye, G., Ahmadibeni, Y.,
Parang, K.
Synthesis of polymer-bound 4-acetoxy-3-phenylbenzaldehyde derivatives:
Applications in solid-phase organic synthesis.
J. Org. Chem.
(2006) 71,
7915-7918.
12.
Ayrapetov, M. K., Wang, Y.-H., Xiaofeng, L., Gu X.,
Parang,
K.,
Sun G.
Conformational basis for
SH2-pTYR527 binding in SRC inactivation.
J. Biol. Chem.
(2006) 281,
23776-23784.
13.
Kumar, A., Ye, G., Wang, Y., Lin, X., Sun, G.,
Parang, K.
Synthesis and structure-activity relationships of linear and
conformationally constrained peptide analogs of CIYKYY as Src tyrosine
kinase inhibitors. J. Med. Chem.
(2006) 49,
3395-3401.
14.
Ahmadibeni, Y.,
Parang, K.
Application of a solid-phase β-triphosphitylating
reagent in the synthesis of nucleoside β-triphosphates.
J. Org. Chem. (2006)
71, 5837-5839.
15.
Ahmadibeni, Y.,
Parang, K.
Solid-phase synthesis of dinucleoside and nucleoside-carbohydrate
phosphodiesters and thiophosphodiesters. J.
Org. Chem. (2006)
71, 6693-6696.
16.
Lee, S., Ayrapetov, M. K., Kemble, D.,
Parang, K.,
Sun, G. Docking-based substrate recognition by the catalytic domain of a
protein tyrosine kinase, the C-terminal Src kinase.
J. Biol. Chem. (2006)
281, 8183-8189.
17.
Lin, X., Wang, Y., Ahmadibeni, Y.,
Parang, K.,
Sun, G. Structural basis for domain-domain communication in a protein
tyrosine kinase, Csk. J. Mol. Biol.
(2006) 357,
1263-1273.
18.
Ahmadibeni, Y.,
Parang, K.
Selective diphosphorylation, dithiodiphosphorylation, triphosphorylation,
and trithiotriphosphorylation of unprotected carbohydrates and nucleosides.
Org. Lett. (2005)
7,
5589-5592.
19.
Parang, K.,
Sun, G. Recent advances in the discovery of Src kinases inhibitors.
Expert Opin. Ther. Patents
(2005) 15,
1183-1207.
20.
Ayrapetov, M. K., Nam, N. H., Ye, G. Kumar, A.,
Parang, K.,
Sun, G.
Functional diversity of Csk, Chk, and Src SH2 domains due to a single
residue variation. J. Biol. Chem.
(2005) 280,
25780-25787.
21.
Ahmadibeni, Y.,
Parang, K.
Polymer-bound
oxathiaphospholane: A solid-phase reagent for regioselective
monothiophosphorylation and monophosphorylation of unprotected nucleosides
and carbohydrates. Org. Lett.
(2005) 7,
1955-1958.
22.
Ahmadibeni, Y.,
Parang, K.
Solid-phase
reagents for selective monophosphorylation of carbohydrates and nucleosides.
J. Org. Chem.
(2005) 70,
1100-1103.
23.
Nam,
N. H., Lee, S., Ye, G., Sun, G.,
Parang, K.
ATP-phosphopeptide conjugates as inhibitors of Src tyrosine kinases.
Bioorg. Med. Chem. (2004)
12, 5753-5766.
24.
Nam,
N. H., Sardari, S., Selecky, M.,
Parang, K.
Carboxylic acids and phosphate ester derivatives of fluconazole: synthesis
and antifungal activities. Bioorg. Med. Chem.
(2004) 12,
6255-6269.
25.
Nam,
N.-H., Ye, G., Sun, G.,
Parang, K.
Conformationally constrained peptide analogues of pTyr-Glu-Glu-Ile
as inhibitors of the Src SH2 domain binding. J.
Med. Chem. (2004)
47, 3131-3141.
26.
Nam,
N. H., Pitts, R., Sun, G., Sardari, S., Tiemo, A., Xie, M., Yan, B.,
Parang, K.
Design of tetrapeptide ligands as inhibitors of the Src SH2 domain.
Bioorg. Med. Chem. (2004)
12, 779-787
27.
Force, T.,
Kuida, K.,
Parang, K., Kyriakis, J. M. Inhibitors of
protein kinase signaling pathways: emerging therapies for cardiovascular
disease. Circulation
(2004)
109,
1196-1205.
28.
Lee, S., Lin, X., Nam, N. H.,
Parang, K.,
Sun G.
Determination of the substrate-docking site of protein tyrosine kinase Csk.
Proc. Nat. Acad. Sci.
U.S.A. (2003)
100, 14707-14712.
29.
Nam,
N. H., Sardari, S.,
Parang, K.
Reactions of solid supported reagents and solid supports with alcohols and
phenols through their hydroxyl functional group.
J. Comb. Chem. (2003)
5, 479-546.
30.
Parang, K.,
Fournier, E. J.-L., Hindsgaul, O. A solid phase reagent for the capture
phosphorylation of carbohydrate and nucleosides.
Org. Lett. (2001)
3, 307-309.
31.
Parang, K.,
Till, J. H., Ablooglu, A. J., Kohanski, R. A., Hubbard, S. R.,
Cole, P. A.
Mechanism-based design of a protein kinase inhibitor.
Nature Struct. Mol. Biol
(2001) 8, 37-41.
32.
Parang, K.
Polymer-supported reagents for methylphosphorylation and phosphorylation of
Carbohydrates. Bioorg. Med. Chem. Lett.
(2002) 12,
1863-1866.
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