U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Derivatives of A-30912A nucleus

Patent 4293483 Issued on October 6, 1981. Estimated Expiration Date: Icon_subject August 25, 2000. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3150059

Antibiotic aculeacins
Patent #: 3978210
Issued on: 08/31/1976
Inventor: Mizuno ,   et al.

Antibiotic A-30912 and process for production thereof
Patent #: 4024245
Issued on: 05/17/1977
Inventor: Hoehn ,   et al.

Antibiotic A-22082 and process for production thereof
Patent #: 4024246
Issued on: 05/17/1977
Inventor: Higgens ,   et al.

Process of preparing desacyl-pepsidine with bacillus pumilus
Patent #: 4050989
Issued on: 09/27/1977
Inventor: Kuwana ,   et al.

Antibiotic S 31794/F-1 Patent #: 4173629
Issued on: 11/06/1979
Inventor: Dreyfuss ,   et al.

Inventor

Assignee

Application

No. 06/181030 filed on 08/25/1980

US Classes:

530/317, Cyclic peptides435/68.1, Enzymatic production of a protein or polypeptide (e.g., enzymatic hydrolysis, etc.)435/71.1Using a micro-organism to make a protein or polypeptide

Examiners

Primary: Phillips, Delbert R.

Attorney, Agent or Firm

International Classes

C07K 7/56 (20060101)
C07K 7/00 (20060101)
A61K 38/00 (20060101)

Abstract

Compounds of the formula ##STR1## wherein R1 is an N-alkanoyl amino acyl group of the formula ##STR2## wherein: W is a divalent aminoacyl radical of the formula: ##STR3## wherein A is C1 -C10 alkylene or C5 -C6 cycloalkylene; ##STR4## wherein R3 is hydroxymethyl, hydroxyethyl, mercaptomethyl, mercaptoethyl, methylthioethyl, 2-thienyl, 3-indole-methyl, phenyl, benzyl, or substituted phenyl or substituted benzyl in which the benzene ring thereof is substituted with chloro, bromo, iodo, nitro, C1 -C3 alkyl, hydroxy, C1 -C3 alkylthio, carbamyl, or C1 -C3 alkylcarbamyl; ##STR5## wherein X is hydrogen, chloro, bromo, iodo, nitro, C1 -C3 alkyl, hydroxy, C1 -C3 alkoxy, mercapto, C1 -C3 alkylthio, carbamyl, or C1 -C3 alkylcarbamyl; ##STR6## wherein X1 is chloro, bromo, or iodo; ##STR7## wherein B is a divalent radical of the formula: --(CH2)n --, wherein n is an integer from 1 to 3; --CH=CH--; --CH=CH--CH2 --; ##STR8## and R2 is C1 -C17 alkyl or C2 -C17 alkenyl; have antifungal activity.

Other References

  • The Journal of Antibiotics, vol 29, No. 12, 1339-1340, 1976
  • Agr. Biol. Chem. 37 (11), 2455-2463, 1973
  • Agr. Biol. Chem. 37 (12), 2709-2717, 1973
  • Agr. Biol. Chem. 38 (3), 521-529, 1974
  • Agr. Biol. Chem. 38 (10), 1767-1777, (1974)
  • The Journal of Biochemistry, vol. 56, No. 4, 1964, 335-343
  • The Journal of Antibiotics, vol. 31, No. 4, 373-374, (1978)
  • The Journal of Antibiotics (1975), 764-769, vol. 28, No. 10
  • The Journal of Antibiotics 1976, 380-389, vol. 29, No. 4
  • The Journal of Antibiotics 1976, 1268-1274, vol. 29, No. 12
  • The Journal of Antibiotics, vol. 29, No. 12, 1275-1280, 1976
  • Helvetica Chimica Acta, vol. 57, fasc. 8 (1974), 2459-2477
  • Tetrahedran Letters, No. 46, pp. 4147-4150, 1976
  • Helvetica Chimica Acta, vol. 62, fasc. 4 (1979), 1252-1266
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