Appeal No. 1997-0094 Application No. 08/188,232 THE INVENTION The claimed invention is the compound thymosin " gly-amide, i.e., a peptide 1 consisting of amino acid residues 1-29 of the NH -terminal sequence of prothymosin " 2 wherein the glycine residue at position 29 is amidated. OPINION Haritos discloses the NH -terminal sequence of the . 112 amino acid residue 2 polypeptide, prothymosin ", including the sequences for thymosin " and amino acid 1 residues 1-30 for thymosin " (Fig. 6, p. 1011). 11 Abiko I discloses a 30 amino acid residue thymosin " analog having a D-Arg in 11 place of the arginine residue at position 30, which analog has increased resistance to inactivation by enzyme (exopeptidase) degradation (abstract; p. 752). Abiko II discloses synthetic deacetyl-thymosin " (Fig. 2, p. 5420) as 11 approximately equal in potency to synthetic deacetyl-thymosin " in increasing E-rosette- 1 forming capacity in cases of rheumatoid arthritis (p. 5419; Fig. 2, p. 5420). Ishimura discloses four peptides amides derived from thymosin " , i.e., amino acid residue (20- 1 28), (20-27), (20-26) and [Ala-27](20-28) amides (see Figure 2(a), p. 703, peptides 19- 22). According to Ishimura, "the major immunoreactive site of the COOH-terminal half of thymosin " is segment (21-28), with important contributions by 1 - 5 -Page: Previous 1 2 3 4 5 6 7 8 9 10 NextLast modified: November 3, 2007