Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
109 words
A cyclopeptide of the formula ##STR56## in which R is Asn, trp is D-Trp or L-Trp, which can be substituted in the benzene ring by halogen atoms or nitro groups, W is a free or etherified hydroxyl group or halogen atom present as a substituent on the benzene ring of the L-phenylalanine radical, or is hydrogen, X is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid of the formula ##STR57## respectively in which n is an integer from 1 to 7 or de-X and Y is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid as defined above or de-Y, or an acid addition salt or complex thereof.
Claim 2
Dependent Claim
109 words
A cyclopeptide of the formula ##STR56## in which R is Asn, trp is D-Trp or L-Trp, which can be substituted in the benzene ring by halogen atoms or nitro groups, W is a free or etherified hydroxyl group or halogen atom present as a substituent on the benzene ring of the L-phenylalanine radical, or is hydrogen, X is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid of the formula ##STR57## respectively in which n is an integer from 1 to 7 or de-X and Y is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid as defined above or de-Y, or an acid addition salt or complex thereof.
Claim 3
Dependent Claim
73 words
The compound according to claim 1 of the formula I, in which R is Asn, trp is D-Trp or L-Trp, W is hydrogen, X is the radical of an ω-amino-lower alkane-mono-carboxylic acid of the formula --NH--(CH.sub.2).sub.n --CO-- in which n is an integer from 2 to 4, or de-X and Y is the radical of an ω-amino-lower alkane-monocarboxylic acid as defined above or de-Y, or an acid addition salt or a complex thereof.
Claim 4
Dependent Claim
33 words
A compound according to claim 2, in which R is Asn, the tryptophan 8 radical has the D-configuration and --X--Y-- together are --[Gaba] p --, in which p is 0, 1 or 2.
Claim 5
Dependent Claim
209 words
A compound selected from the group consisting of a cyclic peptide of the formula ##STR58## in which R is Asn, trp is D-Trp or L-Trp, which can be substituted in the benzene ring by halogen atoms or nitro groups, W is a free or etherified hydroxyl group or halogen atom present as a substituent on the benzene ring of the L-phenylalanine radical, or is hydrogen, X is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid of the formula ##STR59## respectively in which n is an integer from 1 to 7 or de-X and Y is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid or as defined above de-Y, A is an ε-amino protective group or hydrogen and B is a hydroxyl protective group or hydrogen, it being possible for only one of the symbols A and B to be hydrogen, and a corresponding linear piptide of the formula H--[II']--C (III) in which II' is a radical corresponding to the formula II characterised above, in which the amide bond between any two adjacent aminoacid radicals of the peptide ring is interrupted, and C is a free hydroxyl group, a hydroxyl group modified by an activating group or the hydrazine group --NH--NH 2 , and acid addition salts thereof.
Claim 6
Dependent Claim
209 words
A compound selected from the group consisting of a cyclic peptide of the formula ##STR58## in which R is Asn, trp is D-Trp or L-Trp, which can be substituted in the benzene ring by halogen atoms or nitro groups, W is a free or etherified hydroxyl group or halogen atom present as a substituent on the benzene ring of the L-phenylalanine radical, or is hydrogen, X is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid of the formula ##STR59## respectively in which n is an integer from 1 to 7 or de-X and Y is the radical of an ω-amino-lower alkane-(mono or di)-carboxylic acid or as defined above de-Y, A is an ε-amino protective group or hydrogen and B is a hydroxyl protective group or hydrogen, it being possible for only one of the symbols A and B to be hydrogen, and a corresponding linear piptide of the formula H--[II']--C (III) in which II' is a radical corresponding to the formula II characterised above, in which the amide bond between any two adjacent aminoacid radicals of the peptide ring is interrupted, and C is a free hydroxyl group, a hydroxyl group modified by an activating group or the hydrazine group --NH--NH 2 , and acid addition salts thereof.
Claim 7
Dependent Claim
88 words
A linear peptide according to claim 4, of the formula H-R-Phe-Phe-trp-Lys(A)-Thr(B)-Phe-X-Y-C (IIIc) in which R is Asn, trp is D-Trp or L-Trp, X is the radical of an ω-amino-lower alkane-monocarboxylic acid of the formula --NH--(CH.sub.2).sub.n --CO-- in which n is an integer from 1 to 7, or de-X and Y is the radical of an ω-amino-lower alkane-monocarboxylic acid as defined above or de-Y, A is an ε-amino protective group, B is a hydroxyl protective group and C is a free carboxyl group, or an acid addition salt thereof.
Claim 8
Dependent Claim
7 words
A compound characterised by the formula ##STR60##
Claim 9
Dependent Claim
7 words
A compound characterised by the formula ##STR60##
Claim 10
Dependent Claim
7 words
A compound characterised by the formula ##STR61##
Claim 11
Dependent Claim
7 words
A compound characterised by the formula ##STR61##
Claim 12
Dependent Claim
26 words
A compound characterised by the formula ##STR62## in which A is the tert.-butoxycarbonyl group and B is the tert.-butyl group and p is 1 or 2.
Claim 13
Dependent Claim
26 words
A compound characterised by the formula ##STR62## in which A is the tert.-butoxycarbonyl group and B is the tert.-butyl group and p is 1 or 2.
Claim 14
Dependent Claim
50 words
A pharmaceutical preparation for the treatment of excessive secretion of somatotrophin insulin and/or glucagon which contains an effective amount of at least one of the compounds characterised in any one of claims 3-9, 2 or 1 in combination or admixture with at least one inert, physiologically tolerable carrier and/or adjunct.
Claim 15
Independent Claim
33 words
A method for the therapeutic treatment of excessive secretion of somatotropin, insulin and/or glucagon by administering a therapeutically effective dose of a compound characterised in any one of claims 3-7, 2 or 1.