检测方案
≥99.0% (HPLC)
形式
solid
反应适用性
reagent type: cross-linking reagent
mp
~180 °C (dec.)
官能团
Fmoc
amine
carboxylic acid
储存温度
2-8°C
SMILES字符串
O=C(O)COC1=CC=C(C=C1)C(NC(OCC2C(C=CC=C3)=C3C4=C2C=CC=C4)=O)C5=CC=C(OC)C=C5OC
InChI
1S/C32H29NO7/c1-37-22-15-16-27(29(17-22)38-2)31(20-11-13-21(14-12-20)39-19-30(34)35)33-32(36)40-18-28-25-9-5-3-7-23(25)24-8-4-6-10-26(24)28/h3-17,28,31H,18-19H2,1-2H3,(H,33,36)(H,34,35)
InChI key
UPMGJEMWPQOACJ-UHFFFAOYSA-N
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Bioorganic & medicinal chemistry, 27(13), 2822-2831 (2019-05-14)
Structural and functional effects of core M1 type glycan modification catalyzed by protein O-linked mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGnT1) were investigated using a core M1 glycoform focused library of an α-dystroglycan fragment, 372TRGAIIQTPTLGPIQPTRV390. Evanescent-field fluorescence-assisted microarray system illuminated the specific binding
Scientific reports, 8(1), 13490-13490 (2018-09-12)
Serine proteases are released by neutrophils to act primarily as antimicrobial proteins but excessive and unbalanced serine protease activity results in serious host tissue damage. Here the synthesis of a novel chemical sensor based on a multi-branched fluorescence quencher is
Journal of materials science. Materials in medicine, 29(5), 62-62 (2018-05-08)
The present work is focused on the design of a bioactive chitosan-based scaffold functionalized with organic and inorganic signals to provide the biochemical cues for promoting stem cell osteogenic commitment. The first approach is based on the use of a
Bio-protocol, 10(13), e3669-e3669 (2021-03-05)
Every living cell relies on signal transduction pathways comprised of protein-protein interactions (PPIs). In many cases, these PPIs are between a folded protein domain and a short linear motif (SLiM) within an unstructured region of a protein. As a result
Journal of labelled compounds & radiopharmaceuticals (2020-03-27)
α-Calcitonin gene related peptide (αCGRP) inhibitors are important medicinal targets due to their ability to produce antimigraine effects, thus, the discovery of long-acting αCGRP inhibitors is of significant interest. Herein we report the synthesis of an isotopically labelled version of
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