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经验公式(希尔记法):
C38H33NO5S
化学文摘社编号:
分子量:
615.74
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
8524562
产品名称
Fmoc-Cys(4-methoxytrityl)-OH, ≥98% (HPLC)
InChI key
LOBUWFUSGOYXQX-DHUJRADRSA-N
InChI
1S/C38H33NO5S/c1-43-29-22-20-28(21-23-29)38(26-12-4-2-5-13-26,27-14-6-3-7-15-27)45-25-35(36(40)41)39-37(42)44-24-34-32-18-10-8-16-30(32)31-17-9-11-19-33(31)34/h2-23,34-35H,24-25H2,1H3,(H,39,42)(H,40,41)/t35-/m0/s1
SMILES string
COc1ccc(cc1)C(SC[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)(c5ccccc5)c6ccccc6
assay
≥98% (HPLC)
form
lumps
optical activity
[α]/D +14.0±1.0°, c = 1 in THF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Solid-Phase Thiol-Ene Lipidation of Peptides for the Synthesis of a Potent CGRP Receptor Antagonist.
Elyse T Williams et al.
Angewandte Chemie (International ed. in English), 57(36), 11640-11643 (2018-07-07)
We report a new method herein coined SP-CLipPA (solid-phase cysteine lipidation of a peptide or amino acid) for the synthesis of mono-S-lipidated peptides. This technique utilizes thiol-ene chemistry for conjugation of a vinyl ester to a free thiol of a
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