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5'-Deoxy-5-fluorouridine is a potent and potentially toxic chemical compound, derived from the chemotherapy drug fluorouracil, which plays a significant role in cancer treatment. It functions by disrupting the DNA replication process, leading to the destruction of rapidly dividing cancer cells.

38817-29-7

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38817-29-7 Usage

Uses

Used in Oncology:
5'-Deoxy-5-fluorouridine is used as an anticancer agent for the treatment of various solid tumors, particularly breast, colon, and gastrointestinal (GI) cancers. It is effective due to its ability to interfere with DNA replication in cancer cells, causing their destruction.
However, the use of 5'-Deoxy-5-fluorouridine comes with the risk of serious side effects and toxicity, which may include gastrointestinal issues, bone marrow suppression, and neurotoxicity. Therefore, its administration in a medical setting requires close monitoring and expert handling to ensure patient safety and therapeutic efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 38817-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38817-29:
(7*3)+(6*8)+(5*8)+(4*1)+(3*7)+(2*2)+(1*9)=147
147 % 10 = 7
So 38817-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11FN2O5/c10-3-4-6(14)7(15)8(17-4)12-2-1-5(13)11-9(12)16/h1-2,4,6-8,14-15H,3H2,(H,11,13,16)

38817-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-(fluoromethyl)-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-fluorodeoxyuridine

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:38817-29-7 SDS

38817-29-7Downstream Products

38817-29-7Relevant academic research and scientific papers

Fluorinase-coupled base swaps: Synthesis of [18F]-5′- deoxy-5′-fluorouridines

Winkler, Margit,Domarkas, Juozas,Schweiger, Lutz F.,O'Hagan, David

supporting information; experimental part, p. 10141 - 10143 (2009/05/30)

(Chemical Equation Presented) Making F-ases: One-pot fluorination/base-swap biotransformations were developed by coupling the fluorinase enzyme to nucleoside phosphorylases to generate 5′-deoxy-5′-fluoronucleosides (FDAs). These biotransformations are amenable to radiolabeling syntheses starting from [18F]fluoride ion, as exemplified by the synthesis of [18F]-5′-deoxy-5′-fluorouridines (see scheme), and demonstrate a new application of fluorinase as a catalyst for 18F-C bond formation.

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