Detail of > 2018-61-3
- CAS Number:
- 2018-61-3
- Name:
N-Acetyl-L-phenylalanine
- Formula:
- C11H13NO3
- Molecular Structure:

- Synonyms:
- Acetylphenylalanine;(2S)-2-acetamido-3-phenyl-propanoic acid;Alanine, N-acetyl-3-phenyl-, L-;L-N-Acetylphenylalanine;Ac-Phe-OH;L-Phenylalanine, N-acetyl-;(2S)-2-acetamido-3-phenyl-propanoate;N-Acetyl-3-phenyl-L-alanine;Acetyl-L-phenylalanine;N-Acetylphenylalanine;Alanine, N-acetyl-3-phenyl-, L- (8CI);H-Phe-OH;
- Molecular Weight:
- 207.23
- EINECS:
- 217-959-8
- Density:
- 1.199 g/cm3
- Melting Point:
- 171-173 °C(lit.)
- Boiling Point:
- 453.9 °C at 760 mmHg
- Flash Point:
- 228.3 °C
- Appearance:
- white to off-white fine cryst. powder or needles
- Safety:
- 24/25Details
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Reference
- Effect of polyamines on yeast cell-free protein synthesizing system
- Effect of polyamines on yeast cell-free protein synthesizing system. I. Influence of spermine and spermidine on aminoacyl-tRNA transfer reaction. Wolska-Mitaszko, Barbara; Jakubowicz, Teresa; Gasior,Eugeniusz (Inst. Microbiol. Biochem., Univ. Marii Curie-Sklodowskiej, Lublin, Pol.Some commonly used reagents like 2018-61-3 and 306-67-2 are used in this experiment.). Acta Microbiol. Pol., 25(3), 187-97 (English) 1976. CODEN: AMPOAX. DOCUMENT TYPE: Journal CA Section: 6 (General Biochemistry) Spermine and spermidine added to a Saccharomyces cerevisiae cell-free protein synthesizing system increased the phenylalanine polymn. reaction several-fold at suboptimal concns. of Mg2+ and .apprx.2-fold at optimal amts. of Mg2+. The addn. of polyamines greatly stimulated the enzymic and nonenzymic binding of phenylalanyl-tRNA and N-acetylphenylalanyl-tRNA to ribosomes. The binding of the acetylated deriv. was higher than phenylalanyl-tRNA; however, the former was bound exclusively to the A site of the ribosome. Contrary to the binding process, the puromycin reaction was not stimulated by spermine added at a concn. which enhanced polyphenylalanine synthesis. One of the possible sites of polyamine action may be the binding of aminoacyl-tRNA to ribosomes. .
- Tripeptides
- Tripeptides.Some chemicals with cas registry numbers like 2018-61-3 and 2901-75-9 are also used. Molteni, Luigi; Vercesi, Gian P.; Antonini, Eraldo (Zambeletti, Dr. L., S.p.A., Italy). Ger. Offen. DE 2615129 28 Oct 1976, 25 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C103-52. PRIORITY: IT 75-22190 9 Apr 1975. DOCUMENT TYPE: Patent CA Section: 34 (Synthesis of Amino Acids, Peptides, and Proteins) Section cross-reference(s): 63 Ac-Phe-Phe-His-R (I, R = OH, OMe, NH2, NHMe) and the all-DL and L,D,L isomers of I (R = OMe) were prepd. as antiulcer agents. Thus, Ac-Phe-OH was coupled to H-Phe-OEt by dicyclohexylcarbodiimide (DCC) to give Ac-Phe-Phe-OEt which was sapond. and coupled to H-His-OMe by DCC to give I (R = OMe). The above tripeptides decreased the no. and strength of ulcers in rats. .
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