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47309

Sigma-Aldrich

Fmoc-D-Trp(Boc)-OH

≥95.0% (HPLC)

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Synonym(s):
Nα-Fmoc-N(in)-Boc-D-tryptophan
Empirical Formula (Hill Notation):
C31H30N2O6
CAS Number:
Molecular Weight:
526.58
Beilstein/REAXYS Number:
7062970
MDL number:
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

Quality Level

assay

≥95.0% (HPLC)

form

solid

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Boc
Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)OC(=O)n1cc(C[C@@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)c5ccccc15

InChI

1S/C31H30N2O6/c1-31(2,3)39-30(37)33-17-19(20-10-8-9-15-27(20)33)16-26(28(34)35)32-29(36)38-18-25-23-13-6-4-11-21(23)22-12-5-7-14-24(22)25/h4-15,17,25-26H,16,18H2,1-3H3,(H,32,36)(H,34,35)/t26-/m1/s1

InChI key

ADOHASQZJSJZBT-AREMUKBSSA-N

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Fmoc-D-Trp(Boc)-OH ≥95.0% (HPLC)

47309

Fmoc-D-Trp(Boc)-OH

Fmoc-Trp(Boc)-OH ≥97.0% (HPLC)

47561

Fmoc-Trp(Boc)-OH

Fmoc-Orn(Boc)-OH ≥96.0% (HPLC)

47560

Fmoc-Orn(Boc)-OH

Fmoc-Lys(Boc)-OH ≥98.0% (HPLC)

47624

Fmoc-Lys(Boc)-OH

functional group

Boc, Fmoc

functional group

Boc, Fmoc

functional group

Boc, Fmoc

functional group

Boc, Fmoc

assay

≥95.0% (HPLC)

assay

≥97.0% (HPLC)

assay

≥96.0% (HPLC)

assay

≥98.0% (HPLC)

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

related product

Product No.
Description
Pricing

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
Ngoc-Duc Doan et al.
Journal of peptide science : an official publication of the European Peptide Society, 21(5), 387-391 (2014-11-18)
The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated by the syntheses of [aza-Lys(6)] growth-hormone-releasing peptide-6 analogs.

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