Fmoc-Pra-OH

CAS: 198561-07-8

Ref. 3D-PRA-5010-PI

Produktinformation

• Name: Fmoc-Pra-OH
• Synonyme: (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-ynoic acid, (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid, (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pentynoic acid, (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-ynoic acid, (S)-2-(Fmoc-Amino)-4-Pentynoic Acid, 4-Pentynoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2S)-, 4-Pentynoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-, Fmoc-(S)-2-Propargylglycine, Fmoc-<span class="text-smallcaps">L</span>-propargylglycine, Fmoc-Pra-Oh, N-Alpha-(9-Fluorenylmethoxycarbonyl)-(S)-2-Amino-4-Pentynoic Acid, N-Alpha-(9-Fluorenylmethoxycarbonyl)-Propargylglycine, N-Alpha-(9-Fluorenylmethyloxycarbonyl)-L-Propargylglycine, Rarechem Bk Pt 0257

Beschreibung

Fmoc-Pra-OH is a bioconjugate used in Click Chemistry. Click Chemistry is a chemical reaction that joins two components together by forming an amide bond between the carboxyl group of one component and the amino group on the other component. Fmoc-Pra-OH was synthesized by reacting the epidermal growth factor (EGF) with a cyclic peptide containing an acid moiety, which was conjugated to the azide group of an azidopropargyl linker. This bioconjugate has been shown to have proliferative activity in vitro and structural studies have been performed to understand its reactivity.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 335.36 g/mol
• Formel: C₂₀H₁₇NO₄
• Reinheit: Min. 98.0 Area-%