Fmoc-D-Pro-OH

Name: Fmoc-D-Pro-OH | 101555-62-8
Brand: US-CATO
SKU: S57C3D-2796_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C3D-2796_10_MG

Vendor: US-CATO

Product Information

Product Name

Fmoc-D-Pro-OH

Brand Name

US-CATO

Product Number

C3D-2796

CAS

101555-62-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

688136

IUPAC Name

(2R)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid

InChI Key

ZPGDWQNBZYOZTI-GOSISDBHSA-N

SMILES

C1CC@@H(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O

References Data Source From Pubchem

Rapid clearance of achiral small-molecule drugs using de novo-designed proteins and their cyclic and mirror-image variants

Publication Name: Nature Biomedical Engineering

Publication Date: 2025-05-29

DOI: 10.1038/s41551-025-01404-w

Accurate de novo design of heterochiral protein–protein interactions

Publication Name: Cell Research

Publication Date: 2024-08-14

DOI: 10.1038/s41422-024-01014-2

Covalent Reactive Peptides to Block Protein–Protein Interactions and Inhibit Microbe–Host Interaction

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2022-06-28

DOI: 10.1007/978-1-0716-2489-0_5

Rapid de novo discovery of peptidomimetic affinity reagents for human angiotensin converting enzyme 2

Publication Name: Communications Chemistry

Publication Date: 2022-01-19

DOI: 10.1038/s42004-022-00625-3

Peptide Synthesis: Methods and Protocols

Publication Name: AAPS Advances in the Pharmaceutical Sciences Series

Publication Date: 2022

DOI: 10.1007/978-3-031-04544-8_2

Fmoc-D-Pro-OH

Product Information

General Information

References Data Source From Pubchem

Rapid clearance of achiral small-molecule drugs using de novo-designed proteins and their cyclic and mirror-image variants

Accurate de novo design of heterochiral protein–protein interactions

Covalent Reactive Peptides to Block Protein–Protein Interactions and Inhibit Microbe–Host Interaction

Rapid de novo discovery of peptidomimetic affinity reagents for human angiotensin converting enzyme 2

Peptide Synthesis: Methods and Protocols

Fmoc-D-Pro-OH

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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Fmoc-D-Pro-OH

Product Information

General Information

References Data Source From Pubchem

Rapid clearance of achiral small-molecule drugs using de novo-designed proteins and their cyclic and mirror-image variants

Accurate de novo design of heterochiral protein–protein interactions

Covalent Reactive Peptides to Block Protein–Protein Interactions and Inhibit Microbe–Host Interaction

Rapid de novo discovery of peptidomimetic affinity reagents for human angiotensin converting enzyme 2

Peptide Synthesis: Methods and Protocols

Fmoc-D-Pro-OH

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Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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