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55726-41-5

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55726-41-5 Usage

Classification

Synthetic acylated pyrimidine nucleoside analog.

Derivative

It is a derivative of cytarabine, a commonly used chemotherapy agent.

Potential applications

Antiviral and anticancer agent.

Anti-tumor activity

Promising anti-tumor activity in preclinical studies, particularly in breast and lung cancer models.

Antiviral activity

Demonstrated activity against a range of viruses, including herpes simplex virus and hepatitis B virus.

Research status

Ongoing research to explore its potential as a valuable addition to cancer and viral infection treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 55726-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55726-41:
(7*5)+(6*5)+(5*7)+(4*2)+(3*6)+(2*4)+(1*1)=135
135 % 10 = 5
So 55726-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H31N3O6/c1-2-3-4-5-6-7-8-9-15(24)20-14-10-11-22(19(27)21-14)18-17(26)16(25)13(12-23)28-18/h10-11,13,16-18,23,25-26H,2-9,12H2,1H3,(H,20,21,24,27)/t13-,16-,17+,18-/m1/s1

55726-41-5SDS

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 N-[1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]decanamide

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:55726-41-5 SDS

55726-41-5Downstream Products

55726-41-5Relevant articles and documents

Preparation method for nano-assembly of novel cytarabine prodrug and application

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Paragraph 0041, (2018/09/11)

The invention discloses a preparation method for a nano-assembly of a novel cytarabine prodrug and application. According to the invention, biocompatible decanoic acid is chosen as a hydrophobic material to be covalently bound with cytarabine, so that the novel cytarabine amphiphilic small-molecule prodrug, i.e., decanoate-cytarabine (DA-Ara), is synthesized, the prodrug can be self-assembled intonanorods in water by a nano-precipitation method, and when the nanorods are redispersed into water, a highly stable nanoscale oral medication preparation can be obtained. The result of an in-vitro cytotoxicity experiment indicates that the prodrug DA-Ara shows high sensitivity to human chronic cell leukemia cells K562, and can quickly take effect in inhibiting cells, the effect is persistent, andcytotoxicity is higher. The drug loading capacity of the oral preparation of the prodrug is high, the concentration of nano-suspension is high, the storage time is long, the stability is good, the oral preparation is easier to produce, store and transport, the safety is high, and a broad application prospect is provided for the oral medication method of cytarabine.

N4 -acylarabinonucleosides

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, (2008/06/13)

An N4 -acyl-1-β-D-arabinofuranosylcytosine having the following formula SPC1 Wherein R is an aliphatic acyl group having 3 to 35 carbon atoms. The compounds of this invention are useful as a cancer chemotherapeutic agent for controlling tumors, e.g., in mice, an insecticide, and a fungicidal surface active agent.

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