N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-beta-cyclopentylglycine

Name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-beta-cyclopentylglycine
Brand: Creative Peptides
SKU: R2111
Availability: MadeToOrder

This amino acid analog contains a cyclopentyl ring at the β-position, introducing rigidity and hydrophobic character. Researchers use it to restrict backbone mobility and analyze steric-driven folding. The D-configuration provides stereochemical contrast in peptide design. Its Fmoc protection enables routine synthetic manipulation.

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

N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-beta-cyclopentylglycine(CAS 136555-16-3)

CAT No: R2111

CAS No:136555-16-3

Synonyms/Alias:136555-16-3;FMOC-D-CPG-OH;Fmoc-cyclopentyl-D-Gly-OH;(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclopentylacetic acid;Fmoc-D-cyclopentylglycine;Fmoc-(R)-2-cyclopentylglycine;(2R)-2-cyclopentyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic acid;Fmoc-D-Gly(cyclopentyl)-OH;13555-16-3;N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-cyclopentylglycine;N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-beta-cyclopentylglycine;(R)-cyclopentyl({[(9H-fluoren-9-ylmethoxy)carbonyl]amino})acetic acid;(2R)-2-cyclopentyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetic acid;MFCD01311778;Fmoc-cyclopentyl-D-Gly-OH;(R)-2-Cyclopentyl-2-(Fmoc-amino)-acetic acid;DTXSID60673976;AKOS015911465;AS-73214;CS-0372494;E70569;EN300-7158832;(2R)-Cyclopentyl({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetic acid;(R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-cyclopentylacetic acid;959-956-0;

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

C22H23NO4

M.W/Mr.

365.4

Sequence

Three Letter Code:Fmoc-D-Gly(cPent)-OH

InChI

InChI=1S/C22H23NO4/c24-21(25)20(14-7-1-2-8-14)23-22(26)27-13-19-17-11-5-3-9-15(17)16-10-4-6-12-18(16)19/h3-6,9-12,14,19-20H,1-2,7-8,13H2,(H,23,26)(H,24,25)/t20-/m1/s1

InChI Key

JGWHUIQSEKGLAQ-HXUWFJFHSA-N

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2. Extended exenatide administration enhances lipid metabolism and exacerbates pancreatic injury in mice on a high fat, high carbohydrate diet

3. Low bone turnover and low BMD in Down syndrome: effect of intermittent PTH treatment

4. SERS spectrum of the peptide thymosin‐β4 obtained with Ag nanorod substrate

5. Immune-awakening Saccharomyces-inspired nanocarrier for oral target delivery to lymph and tumors

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