143824-78-6
Chemical Structure
Fmoc-Trp(Boc)-OH
Synonym(s): Fmoc-L-Trp(Boc)-OH
- CAS No.: 143824-78-6
- Formula:C31H30N2O6
- Molecular Weight:526.58
IUPAC Name: Na-(((9H-fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)-L-tryptophan
InChIKey: ADOHASQZJSJZBT-SANMLTNESA-N
SMILES: O=C([C@@H](NC(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O)CC4=CN(C5=CC=CC=C45)C(OC(C)(C)C)=O)O
Biological Activity: Fmoc-Trp(Boc)-OH (Fmoc-L-Trp(Boc)-OH) is an amino acid derivative with protective groups. Fmoc-Trp(Boc)-OH can self-assemble into stable and pH-responsive spherical nanoparticles, which can load and release bioactive molecules, with good biocompatibility and high cell uptake rate. Fmoc-Trp(Boc)-OH can be used in research on drug delivery[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fmoc-Trp(Boc)-OH | 99.66% | Fmoc-Trp(Boc)-OH (Fmoc-L-Trp(Boc)-OH) is an amino acid derivative with protective groups. Fmoc-Trp(Boc)-OH can self-assemble into stable and pH-responsive spherical nanoparticles, which can load and release bioactive molecules, with good biocompatibility and high cell uptake rate. Fmoc-Trp(Boc)-OH can be used in research on drug delivery. | ||||||||||||||||||||
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Fmoc-Trp(Boc)-OH-13C11,15N2 | Fmoc-Trp(Boc)-OH-13C11,15N2 (Fmoc-L-Trp(Boc)-OH-13C11,15N2) is the 13C-labeled and 15N-labeled Fmoc-Trp(Boc)-OH (HY-W008034). Fmoc-Trp(Boc)-OH (Fmoc-L-Trp(Boc)-OH) is an amino acid derivative with protective groups. Fmoc-Trp(Boc)-OH can self-assemble into stable and pH-responsive spherical nanoparticles, which can load and release bioactive molecules, with good biocompatibility and high cell uptake rate. Fmoc-Trp(Boc)-OH can be used in research on drug delivery. | |||||||||||||||||||||
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- [1]. Dube, et al. Nanoparticles generated from a tryptophan derivative: physical characterization and anti-cancer drug delivery. Amino Acids 49 (2017): 975-993. [Content Brief]
- [2]. Moreira R, et al. A high-yielding solid-phase total synthesis of daptomycin using a Fmoc SPPS stable kynurenine synthon. Org Biomol Chem. 2021 Apr 14;19(14):3144-3153. [Content Brief]