285463
D-胱氨酸
98%, for peptide synthesis
别名:
(S,S)-3,3′-二硫代双(2-氨基丙酸)
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关于此项目
线性分子式:
[-SCH2CH(NH2)CO2H]2
化学文摘社编号:
分子量:
240.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
206-486-2
MDL number:
Beilstein/REAXYS Number:
1728093
产品名称
D-胱氨酸, 98%
InChI key
LEVWYRKDKASIDU-QWWZWVQMSA-N
InChI
1S/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m1/s1
SMILES string
N[C@H](CSSC[C@@H](N)C(O)=O)C(O)=O
assay
98%
optical activity
[α]20/D +212°, c = 1 in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
mp
265 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Masashi Harada et al.
Journal of chromatography. A, 1593, 91-101 (2019-02-12)
Novel sophisticated derivatizing agents for the efficient enantioselective separation and mass spectrometric detection of d- and l-amino acids have been developed. Two new axially chiral reagents derived from 6,6'-dimethyl-2,2'-biphenyldiamine were synthesized. Their chiral separation and detection abilities were evaluated by
Theresa K Tiefenbrunn et al.
Protein science : a publication of the Protein Society, 18(5), 970-979 (2009-04-23)
The type 1 repeat domain from thrombospondin has potent antiangiogenic activity and a structurally interesting fold, making it an attractive target for protein engineering. Chemical synthesis is an attractive approach for studying protein domains because it enables the use of
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