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. Author manuscript; available in PMC: 2009 Oct 5.
Published in final edited form as: Biopolymers. 2008;90(5):671–682. doi: 10.1002/bip.21057

Table III.

Structure of the N-Me-2 Sub-Library

Peptide Name Ring Size m n Origin
N-Me-2−1 20 2 2 BL3020−1
N-Me-2−2 21 3 2 BL3020−4
N-Me-2−4 22 4 2 BL3020−10
N-Me-2−5 23 5 2 BL3020−9
N-Me-2−6 21 a 2 BL3020−17
N-Me-2−7 21 2 3 BL3020−8
N-Me-2−8 22 3 3 BL3020−6
N-Me-2−9 22 b 3 BL3020−16c
N-Me-2−10 22 4 3 BL3020−15
N-Me-2−11 23 5 3 BL3020−7
N-Me-2−12 23 b 3 BL3020−17c
N-Me-2−13 22 2 4 BL3020−11
N-Me-2−14 23 3 4 BL3020−12
N-Me-2−15 23 b 4 BL3020−16c
N-Me-2−16 24 4 4 BL3020−13
N-Me-2−17 25 5 4 BL3020−14
N-Me-2−18 26 b 4 BL3020−17c
a

The dicarboxylic acyl spacer (m) was replaced by dimethylglutaric acid spacer. An analytical Vydac C18 column (Vydac 218TP104) was used with a flow rate of 1.0 mL/min. The peptide purity (>95%) was determined by HPLC at a wavelength of 220 nm.

b

The dicarboxylic acyl spacer (m) was replaced by o-phthaloyl spacer.

c

There are differences from the structures at Table I on the ring size and N-methylation position.