## Synthese und chemotaktische Aktivitat des fMLP-Anatogen HCO- Hmb-Leu-Phe-OMe The new fMLP analog HCO-Hmb-Leu-Phe-OMe (l), containing ( 0 2hydroxy-4-(methylthio)butyric acid (Hmb) in place of L-methionine at the N-terminal position, has been synthesized and fully characterized. The peptide 1 ha
Conformational studies of chemotactic HCO-Met-Leu-Phe-OMe analogues
✍ Scribed by G. Vertuani; M. Boggian; A. Breveglieri; G. Cavicchioni; S. Spisani; A. Scatturin
- Book ID
- 104950191
- Publisher
- Springer
- Year
- 1995
- Tongue
- English
- Weight
- 469 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0939-4451
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📜 SIMILAR VOLUMES
## Abstract The α/β^3^‐mixed tripeptides R‐CO‐β^3^‐HMet‐Leu‐Phe‐OMe (**1a**,**b**), R‐CO‐Met‐β^3^‐HLeu‐Phe‐OMe (**2a**,**b**) and R‐CO‐Met‐Leu‐β^3^‐HPhe‐OMe (**3a**,**b**) (**a**, R = __tert__‐butyloxy‐; **b**, R = H−), analogues of the potent chemoattractant For‐Met‐Leu‐Phe‐OMe, have been synthesi
The formylpeptides formyl-methionyl-N-methylleucyl-phenylalanine methyl ester [for-Met-(NMe)Leu-Phe-OMe] 1, formyl-methionyl-2-aminotetralin-2-carboxyl-phenylalanine methyl ester [for-Met-Atc-Phe-OMe] 2, formyl-methionyl-1,2,3,4-tetrahydroisoquinoline-3-carboxyl-phenylalanine methyl ester [for-Met-T