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N-(4-chlorophenyl)-2-phenoxyacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18861-18-2

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18861-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18861-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,6 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18861-18:
(7*1)+(6*8)+(5*8)+(4*6)+(3*1)+(2*1)+(1*8)=132
132 % 10 = 2
So 18861-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClNO2/c15-11-6-8-12(9-7-11)16-14(17)10-18-13-4-2-1-3-5-13/h1-9H,10H2,(H,16,17)

18861-18-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)-2-phenoxyacetamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18861-18-2 SDS

18861-18-2Downstream Products

18861-18-2Relevant academic research and scientific papers

Fragment-Based Discovery of AF9 YEATS Domain Inhibitors

Bian, Kangjie,Gao, Rui,Jin, Ruoxing,Liu, Dan,Liu, Xing,Liu, Yaqian,Lu, Hui,Ruan, Ke,Wang, Lei,Wang, Rui,Wang, Xisheng,Wu, Jihui,Yao, Xuebiao,Zhang, Jiahai,Zhang, Zhiyong

, (2022/04/03)

YEATS (YAF9, ENL, AF9, TAF14, SAS5) family proteins recognize acylated histones and in turn regulate chromatin structure, gene transcription, and stress signaling. The chromosomal translocations of ENL and mixed lineage leukemia are considered oncogenic drivers in acute mye-loid leukemia and acute lymphoid leukemia. However, known ENL YEATS domain inhibitors have failed to suppress the proliferation of 60 tested cancer cell lines. Herein, we identified four hits from the NMR fragment-based screening against the AF9 YEATS domain. Ten inhibitors of new chemo-types were then designed and synthesized guided by two complex structures and affinity assays. The complex structures revealed that these inhibitors formed an extra hydrogen bond to AF9, with respect to known ENL inhibitors. Furthermore, these inhibitors demonstrated antiproliferation activities in AF9-sensitive HGC-27 cells, which recapitulated the phenotype of the CRISPR studies against AF9. Our work will provide the basis for further structured-based optimization and reignite the campaign for potent AF9 YEATS inhibitors as a precise treatment for AF9-sensitive cancers.

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