Method for the treatment of conditions caused by herpes virus in

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

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514 17, 514 18, 514 9, 530328, 530329, 530330, 530317, A61K 3808, A61K 3800, A61K 3812

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active

057634068

ABSTRACT:
Peptides of the general formula (I): I-A-B-C-D-E-F-G-H-II are disclosed as being active against Herpes virus infections in animals and human beings, wherein A is Ala, Gly, Val or absent; B is Ala, Gly, Val, Ser or absent; C is Ser, Thr or absent; D is Ser, Thr, Ans, Glu, Arg, Ile, Leu or absent; E is Ser, Thr, Asp or absent; F is Thr, Ser, Asn, Gln, Lys, Trp or absent; G is Tyr or absent; H is Thr, Gly, Met, Met(O), Cys, Thr or Gly; I is Cys or absent, and II is Cys, an amide group, substituted amide group, an ester group or absent, wherein the peptides comprise at least 4 amino acids and physiologically acceptable salts thereof.

REFERENCES:
Pert, C. B. Small peptides which inhibit binding to T4 receptors on human T-lymphocytes, inhibition of AIDS virus infection by the peptides, and their use as immunogens. Chem. Abstracts #93418, 1989.
Identification of a Putative Cell Receptor for Human Cytomegalovirus, Adlish et al., Virology 176, 337-345 (1990).
New Methods and Reagents in Organic Synthesis. 55.+ 1 Total Synthesis of Patellamides B and C, Cytotoxic Cyclic Peptides From a Tunicate 1. Their Proposed Structures Should Be Corrected.2, Hamada, et al., Tetrahedron Letters, vol. 26, No. 42, pp. 5155-5158, 1985.
Prodrug derivatives of thyrotropin-releasing hormone and other peptides, Bundgaard, et al., Peptide Drug Delivery, vol. 17, 947-949, (1989).

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