H-Ser-Phe-OH | 16875-28-8
中文名称:
H-Ser-Phe-OH
英文名称:
H-Ser-Phe-OH
CAS No.:
16875-28-8
分子式:
C1 2 H1 6 N2 O4
分子量:
252.26644
名称和标识符
MDL
MFCD00037254
InChIKey
PPQRSMGDOHLTBE-UWVGGRQHSA-N
Inchi
InChI=1S/C12H16N2O4/c13-9(7-15)11(16)14-10(12(17)18)6-8-4-2-1-3-5-8/h1-5,9-10,15H,6-7,13H2,(H,14,16)(H,17,18)/t9-,10-/m0/s1
SMILES
O=C(O)[C@@H](NC([C@@H](N)CO)=O)CC1=CC=CC=C1
别名信息
- 英文别名 -
(S)-2-((S)-2-Amino-3-hydroxypropanamido)-3-phenylpropanoic acid
2-[(2-amino-3-hydroxypropanoyl)amino]-3-phenylpropanoic acid
H-Ser-Phe-OH
L-Phenylalanine,L-seryl-
SER-PHE
SER-PHE CRYTALLINE
L-ser-L-phe
L-seryl-L-phenylalanine
Serin-phenylalanin
Ser-Phe-OH
L-Ser-L-Phe-OH
N-L-Seryl-L-phenylalanine
CHEMBL3321990
SF dipeptide
16875-28-8
S-F Dipeptide
SCHEMBL9622556
CHEBI:71029
Serine-Phenylalanine dipeptide
MFCD00037254
L-Serinyl-L-Phenylalanine
(2S)-2-{[(2S)-2-amino-3-hydroxypropanoyl]amino}-3-phenylpropanoic acid
BDBM50049557
CS-0654527
HY-P4509
Seryl-phenylalanine
Q27139262
(2S)-2-[[(2S)-2-amino-3-hydroxypropanoyl]amino]-3-phenylpropanoic acid
(2S)-2-[(2S)-2-AMINO-3-HYDROXYPROPANAMIDO]-3-PHENYLPROPANOIC ACID
Serinylphenylalanine
L-Ser-L-Phe
l-serylphenylalanine
Serine Phenylalanine dipeptide
物化性质
实验特性
LogP
0.20930
PSA
112.65000
计算特性
精确分子量
252.11100
氢键供体数量
4
氢键受体数量
6
可旋转化学键数量
7
同位素质量
252.11100700g/mol
重原子数量
18
复杂度
290
同位素原子数量
0
确定原子立构中心数量
2
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
-3.5
拓扑分子极性表面积
113Ų
相关文献
1.
Polypeptides. Part VIII. Variations of the aspartyl position in the C-terminal tetrapeptide amide sequence of the gastrins
H. Gregory,J. S. Morley,J. M. Smith,M. J. Smithers J. Chem. Soc. C 1968 715
2.
Coordination of copper(ii) ions by the fragments of neuropeptide gamma containing D1, H9, H12 residues and products of copper-catalyzed oxidation
El?bieta Jankowska,Marta Pietruszka,Teresa Kowalik-Jankowska Dalton Trans. 2012 41 1683
3.
Expedient synthesis of pseudo-Pro-containing peptides: towards constrained peptidomimetics and foldamers
Rossella De Marco,Alessandra Tolomelli,Marilena Campitiello,Pasqualina Rubini,Luca Gentilucci Org. Biomol. Chem. 2012 10 2307
4.
Identification and antimicrobial activity evaluation of three peptides from laba garlic and the related mechanism
Xudong Gao,Yue Chen,Zhongqin Chen,Zihan Xue,Yanan Jia,Qingwen guo,Qiqi Ma,Min Zhang,Haixia Chen Food Funct. 2019 10 4486
5.
Synthesis of human growth hormone-(27–44)-octadecapeptide and some smaller fragment peptides
Francesco Chillemi J. Chem. Soc. Perkin Trans. 1 1981 1913
6.
Calcium carbonate crystal growth beneath Langmuir monolayers of acidic β-hairpin peptides
Haofei Gong,Yi Yang,Manuela Pluntke,Othmar Marti,Zsuzsa Majer,Norbert Sewald,Dirk Volkmer Dalton Trans. 2014 43 16857
7.
Oxyma-B, an excellent racemization suppressor for peptide synthesis
Yahya E. Jad,Sherine N. Khattab,Beatriz G. de la Torre,Thavendran Govender,Hendrik G. Kruger,Ayman El-Faham,Fernando Albericio Org. Biomol. Chem. 2014 12 8379
8.
Gas phase ultraviolet and infrared spectroscopy on a partial peptide of β2-adrenoceptor SIVSF-NH2 by a laser desorption supersonic jet technique
Shun-ichi Ishiuchi,Kohei Yamada,Hikari Oba,Hiromichi Wako,Masaaki Fujii Phys. Chem. Chem. Phys. 2016 18 23277
9.
Rapid and selective detection of cysteine over homocysteine and glutathione by a simple and effective coumarin-based fluorescent probe
Yan-Fei Kang,Hai-Xia Qiao,Ya-Li Meng,Sai-Jin Cui,Ya-Jun Han,Zhi-Yong Wu,Jie Wu,Xiao-Hui Jia,Xiao-Lei Zhang,Ming-Yan Dai RSC Adv. 2016 6 94866
10.
Peptide synthesis beyond DMF: THF and ACN as excellent and friendlier alternatives
Yahya E. Jad,Gerardo A. Acosta,Sherine N. Khattab,Beatriz G. de la Torre,Thavendran Govender,Hendrik G. Kruger,Ayman El-Faham,Fernando Albericio Org. Biomol. Chem. 2015 13 2393
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