Merck
CN

03755

Sigma-Aldrich

FMOC-L-1,2,3,4-四氢-Β-咔啉-3-羧酸

≥98.0%

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经验公式(希尔记法):
C27H22N2O4
分子量:
438.47
MDL编号:
PubChem化学物质编号:

检测方案

≥98.0%

旋光性

[α]20/D +56±2°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

官能团

Fmoc

储存温度

2-8°C

SMILES string

OC(=O)[C@@H]1Cc2c(CN1C(=O)OCC3c4ccccc4-c5ccccc35)[nH]c6ccccc26

InChI

1S/C27H22N2O4/c30-26(31)25-13-21-20-11-5-6-12-23(20)28-24(21)14-29(25)27(32)33-15-22-18-9-3-1-7-16(18)17-8-2-4-10-19(17)22/h1-12,22,25,28H,13-15H2,(H,30,31)/t25-/m0/s1

InChI key

IHHULIKSMJSELI-VWLOTQADSA-N

法规信息

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B S Emswiler-Rose et al.
Applied and environmental microbiology, 40(1), 13-18 (1980-07-01)
Staphylococcal food poisoning associated with fermented sausages has been a recurring problem. By testing for thermonuclease by direct application of sausage casing disks on the surface of thermonuclease assay agar plates, possible Staphylococcus aureus growth in fermented sausages could be
R T Kamakaka et al.
Genes & development, 7(9), 1779-1795 (1993-09-01)
Purified, reconstituted chromatin templates containing regular, physiological nucleosome spacing were transcribed in vitro by RNA polymerase II along with the Gal4-VP16 activator. When Gal4-VP16 was prebound to DNA before reconstitution of either H1-deficient or H1-containing chromatin, the resulting templates were
S M Paranjape et al.
Genes & development, 9(16), 1978-1991 (1995-08-15)
We have examined the effect of HMG17 on transcription by RNA polymerase II by the assembly and analysis of HMG17-containing chromatin templates consisting of regularly spaced nucleosomal arrays. Structural analysis of the chromatin indicated that HMG17 is incorporated into chromatin
Priya Prasad et al.
Frontiers in microbiology, 10, 1303-1303 (2019-06-30)
Chromatin architecture influences gene expression and makes specialized chromatin domains. Factors including histone variants, histone modifiers and chromatin remodelers that define chromatin architecture impact chromosome related processes in Candida albicans. In this context, we sought to investigate the roles of
Paul R Mueller et al.
Methods in molecular biology (Clifton, N.J.), 296, 299-328 (2004-12-04)
The Wee kinases (Wee1, Wee2, and Myt1) are major regulators of mitotic entry. They function by phosphorylating Cdc2 and related Cdks on conserved tyrosine and threonine residues. This phosphorylation blocks the activity of the Cdc2 and prevents entry into mitosis.

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