N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methyl-O-propyl-L-homoserine

Name: N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methyl-O-propyl-L-homoserine
Brand: Creative Peptides
SKU: R2179
Availability: MadeToOrder

This homoserine analog combines N-methylation with an O-propyl substituent, modulating hydrogen bonding and steric load. Researchers use it to explore side-chain reactivity, conformational restriction, and hydrophobic tuning. The Fmoc protection enables controlled incorporation into peptides. Its design supports structural and mechanistic investigations.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methyl-O-propyl-L-homoserine(CAS 2973755-77-8)

CAT No: R2179

CAS No:2973755-77-8

Synonyms/Alias:N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methyl-O-propyl-L-homoserine;SCHEMBL25357642;2973755-77-8;

Custom Peptide Synthesis

cGMP Peptide

Registration of APIs
CMC information required for an IND

IND and NDA support
Drug master files (DMF) filing

M.F/Formula

C23H27NO5

M.W/Mr.

397.5

Sequence

Three Letter Code:Fmoc-N(Me)Hse(Pr)(Pr)-OH

InChI

InChI=1S/C23H27NO5/c1-3-13-28-14-12-21(22(25)26)24(2)23(27)29-15-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,20-21H,3,12-15H2,1-2H3,(H,25,26)/t21-/m0/s1

InChI Key

MCUDJFMYFODSQO-NRFANRHFSA-N

1. TMEM16F and dynamins control expansive plasma membrane reservoirs

2. Investigating Potential Interactions Between Neurohypophyseal Peptides, their Drug Analogs, and Coagulation Factor VIII

3. Urinary Metabolites Associated with Blood Pressure on a Low-or High-Sodium Die

4. The effect of B-type allatostatin neuropeptides on crosstalk between the insect immune response and cold tolerance

5. Autoinhibition and phosphorylation-induced activation of phospholipase C-γ isozymes

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