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Coformycin is an N-glycosyl compound in which (8R)-3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol is attached to ribofuranose via a beta-N3-glycosidic bond. It is the parent compound of the class of coformycins.

11033-22-0

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11033-22-0 Usage

Uses

Used in Pharmaceutical Industry:
Coformycin is used as an antiviral agent for its ability to inhibit the replication of certain viruses, such as the influenza virus. It functions by blocking the activity of the viral enzyme neuraminidase, which is essential for the release of new virus particles from infected cells.
Used in Research Applications:
Coformycin is used as a research tool for studying the structure and function of neuraminidase enzymes, as well as the mechanisms of viral replication and pathogenesis. It can also be used to investigate the development of new antiviral drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 11033-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 11033-22:
(7*1)+(6*1)+(5*0)+(4*3)+(3*3)+(2*2)+(1*2)=40
40 % 10 = 0
So 11033-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N4O5/c16-2-6-8(18)9(19)11(20-6)15-4-14-7-5(17)1-12-3-13-10(7)15/h3-6,8-9,11,16-19H,1-2H2,(H,12,13)/t5-,6-,8-,9-,11-/m1/s1

11033-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name coformycin

1.2 Other means of identification

Product number -
Other names Coformycin

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:11033-22-0 SDS

11033-22-0Upstream product

11033-22-0Downstream Products

11033-22-0Related news

Regular ArticleHow Important Is theN-3 Sugar Moiety in the Tight-Binding Interaction of coformycin (cas 11033-22-0) with Adenosine Deaminase?☆08/22/2019

Preliminary findings on the possible important role of the N-3 sugar moiety of coformycin in its tight-binding interaction with adenosine deaminase (ADA) are reported. The compound 3-β-D-Ribofuranosyl-5,6,7,8tetrahydro-4H-imidazo[4,5-d][1,3]diazepin-5-one-8-ol (1), its 3-benzyl analogue (6), an...detailed

Isolation of mutant adenosine deaminase by coformycin (cas 11033-22-0) affinity chromatography☆08/18/2019

Adenosine deaminase is a purine salvage enzyme that catalyzes the deamination of adenosine and deoxyadenosine. Deficiency of the enzyme activity is associated with T-cell and B-cell dysfunction. Mutant adenosine deaminase has been isolated from heterozygous and homozygous deficient lymphoblast c...detailed

11033-22-0Relevant academic research and scientific papers

Separation of coformycin and its related nucleosides

-

, (2008/06/13)

A known nucleoside, coformycin and its related substances such as isocoformycin, 2'-deoxycoformycin and formycins present as a mixture of them may be separated from each other when an aqueous solution containing them is chromatographed on a column of a cation-exchanger having partially activated carboxylic groups as the ion-exchange function with using water or a buffer solution as the developing solvent.

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