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5-fluoro-(2',3')-dideoxy-3'-fluorouridine 5'-phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87395-48-0

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87395-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87395-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,9 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87395-48:
(7*8)+(6*7)+(5*3)+(4*9)+(3*5)+(2*4)+(1*8)=180
180 % 10 = 0
So 87395-48-0 is a valid CAS Registry Number.

87395-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,5R)-3-fluoro-5-(5-fluoro-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names 5'-Uridylic acid,2',3'-dideoxy-3',5-difluoro

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:87395-48-0 SDS

87395-48-0Downstream Products

87395-48-0Relevant academic research and scientific papers

Synthesis and Biological Activity of 5-Fluoro-2',3'-dideoxy-3'-fluorouridine and Its 5'-Phosphate

Ajmera, Sudhir,Bapat, Ashok R.,Danenberg, Kathleen,Danenberg, Peter V.

, p. 11 - 14 (1984)

5-Fluoro-2',3'-dideoxy-3'-fluorouridine (3'-FFdUrd) and 5-fluoro-2',3'-dideoxy-3'-fluorouridine 5'-phosphate (3'-FFdUMP) have been synthesized, and their interactions with thymidine (dThd) phosphorylase and thymidylate (dTMP) synthetase, respectively, have been examined. 3'-FFdUrd is not a substrate for dThd phosphorylase, but is a weak, noncompetitive inhibitor (Ki = 1.7 mM). 3'-FFdUMP inhibits dTMP synthetase competitively with deoxyuridylate (Ki = 0.13 mM) when both the substrate and inhibitor are present simultaneously.However, in the presence of 5,10-methylenete trahydrofolate, the inhibition increases with time in a first-order manner (konobsd = 0.029 s-1).A complex is formed between 3'-FFdUMP and dTMP synthetase, which is isolable on nitrocellulose filters, and has a dissociation rate (koffobsd = 1.4*10-2 min-1) similar to that of the potent inhibitor 5-fluoro-2'-deoxyuridilate (koffobsd = 1.3*10-2 min-1) from its ternary complex with dTMP synthetase.These results are explained in terms of a two-stage model involving the initial formation of a revesible adsorption complex, followed by a slow conversion to a tight-binding catalytic complex.

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