Gilon C - Search Results

1

A backbone-cyclic, receptor 5-selective somatostatin analogue: synthesis, bioactivity, and nuclear magnetic resonance conformational analysis.

Gilon C, Huenges M, Mathä B, Gellerman G, Hornik V, Afargan M, Amitay O, Ziv O, Feller E, Gamliel A, Shohat D, Wanger M, Arad O, Kessler H. Gilon C, et al. J Med Chem. 1998 Mar 12;41(6):919-29. doi: 10.1021/jm970633x. J Med Chem. 1998. PMID: 9526566

2

N-methylated analogs of Ac[Nle28,31]CCK(26-33): synthesis, activity, and receptor selectivity.

Ron D, Gilon C, Hanani M, Vromen A, Selinger Z, Chorev M. Ron D, et al. Among authors: gilon c. J Med Chem. 1992 Jul 24;35(15):2806-11. doi: 10.1021/jm00093a013. J Med Chem. 1992. PMID: 1495013

3

Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases.

Gazit A, Osherov N, Posner I, Yaish P, Poradosu E, Gilon C, Levitzki A. Gazit A, et al. Among authors: gilon c. J Med Chem. 1991 Jun;34(6):1896-907. doi: 10.1021/jm00110a022. J Med Chem. 1991. PMID: 1676428

4

Pseudopeptide analogues of substance P and leucine enkephalinamide containing the psi (CH2O) modification: synthesis and biological activity.

Roubini E, Laufer R, Gilon C, Selinger Z, Roques BP, Chorev M. Roubini E, et al. Among authors: gilon c. J Med Chem. 1991 Aug;34(8):2430-8. doi: 10.1021/jm00112a018. J Med Chem. 1991. PMID: 1714957

5

Dehydro keto methylene and keto methylene analogues of substance P. Synthesis and biological activity.

Ewenson A, Laufer R, Chorev M, Selinger Z, Gilon C. Ewenson A, et al. Among authors: gilon c. J Med Chem. 1988 Feb;31(2):416-21. doi: 10.1021/jm00397a026. J Med Chem. 1988. PMID: 2448458

6

Tyrphostins I: synthesis and biological activity of protein tyrosine kinase inhibitors.

Gazit A, Yaish P, Gilon C, Levitzki A. Gazit A, et al. Among authors: gilon c. J Med Chem. 1989 Oct;32(10):2344-52. doi: 10.1021/jm00130a020. J Med Chem. 1989. PMID: 2552117

7

Comparison of the conformation of active and nonactive backbone cyclic analogs of substance P as a tool to elucidate features of the bioactive conformation: NMR and molecular dynamics in DMSO and water.

Grdadolnik SG, Mierke DF, Byk G, Zeltser I, Gilon C, Kessler H. Grdadolnik SG, et al. Among authors: gilon c. J Med Chem. 1994 Jul 8;37(14):2145-52. doi: 10.1021/jm00040a005. J Med Chem. 1994. PMID: 7518522

8

Tyrphostins. 3. Structure-activity relationship studies of alpha-substituted benzylidenemalononitrile 5-S-aryltyrphostins.

Gazit A, Osherov N, Posner I, Bar-Sinai A, Gilon C, Levitzki A. Gazit A, et al. Among authors: gilon c. J Med Chem. 1993 Nov 12;36(23):3556-64. doi: 10.1021/jm00075a010. J Med Chem. 1993. PMID: 7902440

9

Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P.

Byk G, Halle D, Zeltser I, Bitan G, Selinger Z, Gilon C. Byk G, et al. Among authors: gilon c. J Med Chem. 1996 Aug 2;39(16):3174-8. doi: 10.1021/jm960154i. J Med Chem. 1996. PMID: 8759639

10

Tyrphostins. 6. Dimeric benzylidenemalononitrile tyrophostins: potent inhibitors of EGF receptor tyrosine kinase in vitro.

Gazit A, Osherov N, Gilon C, Levitzki A. Gazit A, et al. Among authors: gilon c. J Med Chem. 1996 Dec 6;39(25):4905-11. doi: 10.1021/jm960225d. J Med Chem. 1996. PMID: 8960549

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