82911-78-2
82911-78-2
Chemical Structure
Fmoc-Ser-OMe
Synonym(s): Fmoc-L-Ser-OMe
- CAS No.: 82911-78-2
- Formula:C19H19NO5
- Molecular Weight:341.36
IUPAC Name: methyl (((9H-fluoren-9-yl)methoxy)carbonyl)-L-serinate
InChIKey: QQQVLIVWQMWACQ-KRWDZBQOSA-N
SMILES: OC[C@@H](C(OC)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O
Biological Activity: Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is an Fmoc-protected L-serine methyl ester and also a solid-phase peptide synthesis intermediate. Fmoc-Ser-OMe is linked to Ellman resin via its hydroxyl side chain. Fmoc-Ser-OMe is used in peptide synthesis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Fmoc-Ser-OMe | 99.70% | Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is an Fmoc-protected L-serine methyl ester and also a solid-phase peptide synthesis intermediate. Fmoc-Ser-OMe is linked to Ellman resin via its hydroxyl side chain. Fmoc-Ser-OMe is used in peptide synthesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Structural Analogs
-
Similarity Score 0.89
HY-W007720Fmoc-Ser-OH -
Similarity Score 0.89
HY-W007720S1Fmoc-Ser-OH-15N -
Similarity Score 0.89
HY-W013793(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-serine -
Similarity Score 0.88
HY-22297Fmoc-Ser-OtBu -
Similarity Score 0.86
HY-W041982Fmoc-Asp-OMe -
Similarity Score 0.85
HY-W004101Fmoc-D-Abu-OH -
Similarity Score 0.85
HY-W009151Fmoc-Abu-OH -
Similarity Score 0.84
HY-W048727(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-cysteine -
Similarity Score 0.84
HY-W041988Fmoc-Glu-OMe -
Explore the MedChemAI to find more analogs
References
- [1]. Sharma A, et al. Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis. ChemistryOpen. 2017;6(2):206-210. Published 2017 Mar 8. [Content Brief]
- [2]. Schroll AL, et al. The use of 2,2'-dithiobis(5-nitropyridine) (DTNP) for deprotection and diselenide formation in protected selenocysteine-containing peptides. J Pept Sci. 2012;18(3):155-162. [Content Brief]
