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. Author manuscript; available in PMC: 2010 Mar 12.
Published in final edited form as: J Med Chem. 2009 Mar 12;52(5):1310–1316. doi: 10.1021/jm801397w

Table 2.

Structure and properties of the galanin analogs. All analogs are amidated at the C-terminus.

Analog Structure HPLC retention timea α-helixb Mass spec. (MALDI, MH+) Calcd/found
Gal-(K)4c (Sar)WTLNSAGYLLGPKKKK 15.13 ± 0.42 14% 1873.09/1873.14
Gal-B2-C8 (Sar)WTLNSAGYLLGPKK(Lys-octanoyl)K 20.13 ± 0.17 9% 2001.21/2001.17
Gal-B2-C10 (Sar)WTLNSAGYLLGPKK(Lys-decanoyl)K 21.49 ± 0.05 6% 2029.24/2029.45
Gal-B2-C12 (Sar)WTLNSAGYLLGPKK(Lys-lauroyl)K 22.51 ± 0.03 16% 2057.28/2057.26
Gal-B2-C14 (Sar)WTLNSAGYLLGPKK(Lys-myristoyl)K 23.76 ± 0.18 16% 2085.31/2085.33
Gal-B2c (Sar)WTLNSAGYLLGPKK(Lys-palmitoyl)K 25.84 ± 0.10 23% 2112.31/2112.33
Gal-B2-C18 (Sar)WTLNSAGYLLGPKK(Lys-stearoyl)K 26.73 ± 0.18 5% 2141.33/2141.48
Gal-B2-MPEG4 (Sar)WTLNSAGYLLGPKK(Lys-MPEG4)K 17.52 ± 0.03 18% 2123.23/2123.29
a

A linear gradient of water/90% acetonitrile (buffered with 0.1% TFA) on a Vydac diphenyl column, starting from 20% acetonitrile to 100% acetonitrile in 40 min.

b

Determined in the presence of 50% v/v 2,2,2-trifluoroethanol.

c

Data from 22.