J. Hlavacek et al., AMINO-ACIDS AND PEPTIDES .232. CHOLECYSTOKININ HEPTAPEPTIDE ANALOGS WITH MULTIPLE MODIFICATION IN PEPTIDE-CHAIN, Collection of Czechoslovak Chemical Communications, 58(11), 1993, pp. 2761-2765
Using solid phase synthesis we prepared the cholecystokinin fragment B
oc-CCK-7 (Boc-Tyr(SO3-Na+)-Met-Gly-Trp-Met-Asp-Phe-NH2) Ia and its sev
en analogues Ib - Ih. In the analogues Ib and Ic the Met residue in th
e carboxyterminal part of the molecule was substituted for L- or D-Phe
Me3. In the analogues Id and le with Phe residue substituted by L- or
D-PheMe3 the Neo was inserted in the place of this Met residue and in
the analogues If and Ig, in addition to PheMe3 substitution in the car
boxyterminus, both Met residues were replaced for Neo. This dual subst
itution for Met residues was also applied in the analogue Ih with code
d Phe residue in the C-terminus.