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. Author manuscript; available in PMC: 2012 Aug 1.
Published in final edited form as: Peptides. 2011 Jun 25;32(8):1677–1684. doi: 10.1016/j.peptides.2011.06.011

Table III.

Binding of BB ligands

Addition IC50, nM
BA1 1.1 ± 0.2
BA2 21± 3
BA3 15 ± 2
BB >2000
BRS3 ant. 750 ± 82
BW2258U89 >2000
Gefitinib >2000
GRP >2000
NMB >2000
PD168368 >2000

The ability of ligands to half maximally (IC50) inhibit specific 125I-BA1 binding to NCI-H1299-BRS-3 cells was determined at 37°C. The mean value ± S.E. of 4 determinations is shown.

The peptide structures are:

BB- Pyr-Gln-Arg-Leu-Gly-Asn-Leu-Trp-Ala-Val-Gly-His-Leu-Met-NH2

BA1- (DTyr6, βAla11, Phe13, Nle14)BB6-14

BA2- (DTyr6, R-Apa11, Phe13, Nle14)BB6-14

BA3- (DTyr6, R-Apa11, 4-Cl,Phe13, Nle14)BB6-14

BRS-3 ant. (DNal-Cys-Tyr-DTrp-Lys-Val-Cys-Nal)NH2.