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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433845생성일: 2026년 10월 24일

2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acid → HCID 178418600, 화합물

https://huagongshe.com/ko/reaction/433845

반응식

참여 물질

역할이름HCID투입량
반응물2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acidHCID 3383—
반응물Norleucine, (+-)-HCID 9475—
반응물Fluorescein 5-isothiocyanateHCID 18730—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물TFA triisopropylsilaneHCID 131724268—
용매DimethylformamideHCID 6228—
생성물HCID 178418600HCID 178418600—
생성물HCID 178512911HCID 178512911—

반응 단계

General Procedure for Peptide Synthesis. Tat49-57 (RKKRRQRRR; SEQ ID NO:28), truncated and alanine-substituted peptides derived from Tat49-57, Antennapedia43-58 (RQIKIWFQNRRMKWKKK SEQ ID NO:29), and homopolymers of arginine (R5-R9; SEQ ID NOS:1-5) and d-arginine (r5-r9) were prepared with an automated peptide synthesizer (ABI433) using standard solid-phase Fmoc chemistry (35) with HATU as the peptide coupling reagent. The fluorescein moiety was attached via a aminohexanoic acid spacer by treating a resin-bound peptide (1.0 mmol) with fluorescein isothiocyanate (1.0 mmol) and DIBA (5 mmol) in DMF (10 mL) for 12 h. Cleavage from the resin was achieved using 95:5 TFA/triisopropylsilane. Removal of the solvent in vacuo gave a crude oil which was triturated with cold ether. The crude mixture thus obtained was centrifuged, the ether was removed by decantation, and the resulting orange solid was purified by reverse-phase HPLC (H2O/CH3CN in 0.1% TFA). The products were isolated by lyophilization and characterized by electrospray mass spectrometry. Purity of the peptides was >95% as determined by analytical reverse-phase HPLC (H2O/CH3CN in 0.1% TFA).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06669951B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-d86d5c8f565348078ee4e4a62dca5eff
출처 메모uspto-grants-2003_12