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138516-81-1

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138516-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138516-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138516-81:
(8*1)+(7*3)+(6*8)+(5*5)+(4*1)+(3*6)+(2*8)+(1*1)=141
141 % 10 = 1
So 138516-81-1 is a valid CAS Registry Number.

138516-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-benzyl 5-O-(2,3,4,5,6-pentafluorophenyl) pentanedioate

1.2 Other means of identification

Product number -
Other names Pentanedioic acid,pentafluorophenyl phenylmethyl ester

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:138516-81-1 SDS

138516-81-1Relevant articles and documents

Comprehensive Structure-Activity Relationship of Triantennary N-Acetylgalactosamine Conjugated Antisense Oligonucleotides for Targeted Delivery to Hepatocytes

Prakash, Thazha P.,Yu, Jinghua,Migawa, Michael T.,Kinberger, Garth A.,Wan, W. Brad,?stergaard, Michael E.,Carty, Recaldo L.,Vasquez, Guillermo,Low, Audrey,Chappell, Alfred,Schmidt, Karsten,Aghajan, Mariam,Crosby, Jeff,Murray, Heather M.,Booten, Sheri L.,Hsiao, Jill,Soriano, Armand,MacHemer, Todd,Cauntay, Patrick,Burel, Sebastien A.,Murray, Susan F.,Gaus, Hans,Graham, Mark J.,Swayze, Eric E.,Seth, Punit P.

, p. 2718 - 2733 (2016)

The comprehensive structure-activity relationships of triantennary GalNAc conjugated ASOs for enhancing potency via ASGR mediated delivery to hepatocytes is reported. Seventeen GalNAc clusters were assembled from six distinct scaffolds and attached to ASOs. The resulting ASO conjugates were evaluated in ASGR binding assays, in primary hepatocytes, and in mice. Five structurally distinct GalNAc clusters were chosen for more extensive evaluation using ASOs targeting SRB-1, A1AT, FXI, TTR, and ApoC III mRNAs. GalNAc-ASO conjugates exhibited excellent potencies (ED50 0.5-2 mg/kg) for reducing the targeted mRNAs and proteins. This work culminated in the identification of a simplified tris-based GalNAc cluster (THA-GN3), which can be efficiently assembled using readily available starting materials and conjugated to ASOs using a solution phase conjugation strategy. GalNAc-ASO conjugates thus represent a viable approach for enhancing potency of ASO drugs in the clinic without adding significant complexity or cost to existing protocols for manufacturing oligonucleotide drugs.

TARGETED THERAPEUTIC NUCLEOSIDES AND THEIR USE

-

Page/Page column 167; 171; 172, (2015/04/15)

Provided herein are compounds comprising one or more therapeutic nucleosides and one or more targeting groups. In certain embodiments, the compounds further comprise one or more oligonucleotides. In certain embodiments, a targeting group comprises one or more N-Acetylgalactosamine.

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