DESIGN OF A FUNCTIONAL HEXAPEPTIDE ANTAGONIST OF ENDOTHELIN

[1] SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J]. BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01): : 48 - 58

[2] CHIRAL SYNTHESIS OF D-3,3-DIPHENYLALANINE AND L-3,3-DIPHENYLALANINE (DIP), UNUSUAL ALPHA-AMINO-ACIDS FOR PEPTIDES OF BIOLOGICAL INTEREST [J]. TETRAHEDRON LETTERS, 1992, 33 (23) : 3293 - 3296

[3] MONOCYCLIC ENDOTHELINS - EXAMINATION OF THE IMPORTANCE OF THE INDIVIDUAL DISULFIDE RINGS [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S62 - S64

[4] STRUCTURE ACTIVITY STUDIES OF THE C-TERMINAL REGION OF THE ENDOTHELINS AND THE SARAFOTOXINS [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S59 - S61

[5] DOHERTY AM, 1992, 203RD NAT M AM CHEM

[6] GALANTINO M, 1992, PEPTIDES CHEM BIOL, P404

[7] HEMMI K, 1991, Patent No. 911075547

[8] HSIEH K, 1989, J MED CHEM, V32, P896

[9] BIOLOGICAL PROFILES OF HIGHLY POTENT NOVEL ENDOTHELIN ANTAGONISTS SELECTIVE FOR THE ETA RECEPTOR [J]. LIFE SCIENCES, 1992, 50 (04) : 247 - 255

[10] AN ENDOTHELIN RECEPTOR (ETA) ANTAGONIST ISOLATED FROM STREPTOMYCES-MISAKIENSIS [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 178 (01) : 132 - 137

[1] SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J]. BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01): : 48 - 58

[2] CHIRAL SYNTHESIS OF D-3,3-DIPHENYLALANINE AND L-3,3-DIPHENYLALANINE (DIP), UNUSUAL ALPHA-AMINO-ACIDS FOR PEPTIDES OF BIOLOGICAL INTEREST [J]. TETRAHEDRON LETTERS, 1992, 33 (23) : 3293 - 3296

[3] MONOCYCLIC ENDOTHELINS - EXAMINATION OF THE IMPORTANCE OF THE INDIVIDUAL DISULFIDE RINGS [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S62 - S64

[4] STRUCTURE ACTIVITY STUDIES OF THE C-TERMINAL REGION OF THE ENDOTHELINS AND THE SARAFOTOXINS [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S59 - S61

[5] DOHERTY AM, 1992, 203RD NAT M AM CHEM

[6] GALANTINO M, 1992, PEPTIDES CHEM BIOL, P404

[7] HEMMI K, 1991, Patent No. 911075547

[8] HSIEH K, 1989, J MED CHEM, V32, P896

[9] BIOLOGICAL PROFILES OF HIGHLY POTENT NOVEL ENDOTHELIN ANTAGONISTS SELECTIVE FOR THE ETA RECEPTOR [J]. LIFE SCIENCES, 1992, 50 (04) : 247 - 255

[10] AN ENDOTHELIN RECEPTOR (ETA) ANTAGONIST ISOLATED FROM STREPTOMYCES-MISAKIENSIS [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 178 (01) : 132 - 137