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Postion:Product Catalog >API>Antineoplastic agents>Antimetabolites, Antineoplastic>Nelarabine
Nelarabine
  • Nelarabine

Nelarabine

Price $1
Package 1kg
Min. Order: 1kg
Supply Ability: Customized
Update Time: 2019-07-06

Product Details

Product Name: Nelarabine CAS No.: 121032-29-9
EC-No.: 1806241-263-5 Min. Order: 1kg
Purity: 99% Supply Ability: Customized
Release date: 2019/07/06

SP237

 

Nelarabine Basic information
Physical properties Developed by GlaxoSmithKline Pharmacology and pharmacokinetics Clinical trials Usage and dosage Note
Product Name: Nelarabine
Synonyms: NELARABINE;Nelzarabine [USAN];Nelzarabine;9beta-D-Arabinofuranosyl-6-methoxy-9H-purin-2-amine;(2R,3R,4S,5R)-2-(2-aMino-6-Methoxy-9H-purin-9-yl)-5-(hydroxyMethyl)-tetrahydrofuran-3,4-diol;Nelarabine (Arranon);506u;9-β-D-Arabinofuranosyl-6-Methoxy-9H-purin-2-aMine
CAS: 121032-29-9
MF: C11H15N5O5
MW: 297.27
EINECS: 1806241-263-5
Product Categories: Bases & Related Reagents;Heterocycles;Intermediates & Fine Chemicals;Nucleotides;Pharmaceuticals;5g,10g,25g,100g;ARRANON;Anti-cancer&immunity;API;Inhibitors
Mol File: 121032-29-9.mol
Article illustration
 
Nelarabine Chemical Properties
Melting point  209-217°
alpha  D20 +55.9° (c = 0.27 in DMF)
CAS DataBase Reference 121032-29-9(CAS DataBase Reference)
 
Safety Information
MSDS Information
 
 
Nelarabine Usage And Synthesis
Physical properties White or almost white crystalline powder. This product is slightly soluble in water, the solubility in water is about 8-9mg/ml (25 ℃, PH = 4~10).
Developed by GlaxoSmithKline Nelarabine is a prodrug for deoxyguanosine analogue ——9-beta-D-arabinofuranosyl guanine (ara-G). Nelarabine demethylates in the role of adenosine deaminase (ADA) and turns into ara-G. Then, It turns into active ara-G triphosphate (ara-GTP) in the role of the deoxyguanosine kinase and deoxycytidine kinase and under the action of the monophosphorylation pathway. Ara-GTP can accumulate in leukemia cells, and bind to DNA to inhibit DNA synthesis, and accelerate leukemia cell death. In addition, the anti-cancer mechanism of Nelarabine may also be related to its cytotoxicity and somatic toxicity.
Nelarabine was first successfully developed by GlaxoSmithKline. On October 28, 2005 under the approval of the US Food and Drug Administration, it became a new drug for curing T-cell acute lymphoblastic leukemia (T-ALL) and T-Cells lymphoblasticlymphoma (T-LBL) which are resistant to at least two types of chemotherapy regimens or relapsed after initial treatment. This new drug officially listed in the United States in 2006. This product didn’t apply for patent and administrative protection in China, so the development of this product does not exist intellectual property issues.

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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