N-FORMYL-MET-LEU-PHE-O-FLUOROBENZYLAMIDE
Modify Date: 2024-01-02 06:44:24
N-FORMYL-MET-LEU-PHE-O-FLUOROBENZYLAMIDE structure
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Common Name | N-FORMYL-MET-LEU-PHE-O-FLUOROBENZYLAMIDE | ||
|---|---|---|---|---|
| CAS Number | 112898-02-9 | Molecular Weight | 544.68100 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C28H37FN4O4S | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Name | N-[1-[(2-fluorophenyl)methylamino]-1-oxo-3-phenylpropan-2-yl]-2-[(2-formamido-4-methylsulfanylbutanoyl)amino]-4-methylpentanamide |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C28H37FN4O4S |
|---|---|
| Molecular Weight | 544.68100 |
| Exact Mass | 544.25200 |
| PSA | 155.66000 |
| LogP | 5.92920 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
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The synthetic chemoattractant Trp-Lys-Tyr-Met-Val-DMet activates neutrophils preferentially through the lipoxin A(4) receptor.
Blood 95 , 1810-1818, (2000) A D-methionine-containing peptide, Trp-Lys-Tyr-Met-Val-D-Met-NH(2) (WKYMVm), featuring a unique receptor specificity was investigated with respect to its ability to activate neutrophil effector functi... |
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Conformational energy analysis of the chemotactic tripeptide formyl-Met-Leu-Phe and three analogs.
Int. J. Pept. Protein Res. 34 , 229-234, (1989) Conformational energy analyses were carried out on the chemotactic tripeptide fMLF (CHO-Met-Leu-Phe) and three analogs fALF (CHO-Ala-Leu-Phe). fMF (CHO-Met-Phe), and MLF (H-Met-Leu-Phe). A near-folded... |
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Glia maturation factor-γ mediates neutrophil chemotaxis.
J. Leukoc. Biol. 90 , 529-538, (2011) Chemotaxis is fundamental to the directional migration of neutrophils toward endogenous and exogenous chemoattractants. Recent studies have demonstrated that ADF/cofilin superfamily members play impor... |
| N-Formyl-Met-Leu-Phe-o-fluorobenzylamide |