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Sigma-Aldrich

Fmoc-D-Ser(tBu)-OH

≥98.0% (TLC)

Synonym(s):

Fmoc-O-tert-butyl-D-serine

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About This Item

Empirical Formula (Hill Notation):
C22H25NO5
CAS Number:
128107-47-1
Molecular Weight:
383.44
Beilstein/REAXYS Number:
5309984
MDL number:
MFCD00077071
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57650916
NACRES:
NA.26

assay

≥98.0% (TLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)OC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C22H25NO5/c1-22(2,3)28-13-19(20(24)25)23-21(26)27-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,12-13H2,1-3H3,(H,23,26)(H,24,25)/t19-/m1/s1

InChI key

REITVGIIZHFVGU-LJQANCHMSA-N

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Storage Class

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flash_point_f

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flash_point_c

Not applicable

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Certificates of Analysis (COA)

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Fayçal Touti et al.
Nature chemical biology, 15(4), 410-418 (2019-03-20)
The use of competitive inhibitors to disrupt protein-protein interactions (PPIs) holds great promise for the treatment of disease. However, the discovery of high-affinity inhibitors can be a challenge. Here we report a platform for improving the affinity of peptide-based PPI
Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts

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