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31645-39-3,MFCD01705455
Catalog No.:AA000ZGV

31645-39-3 | Palifosfamide

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10mg
≥95%
in stock  
$48.00   $33.00
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25mg
≥95%
in stock  
$105.00   $73.00
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50mg
≥95%
in stock  
$160.00   $112.00
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100mg
≥95%
in stock  
$252.00   $176.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA000ZGV
Chemical Name:
Palifosfamide
CAS Number:
31645-39-3
Molecular Formula:
C4H11Cl2N2O2P
Molecular Weight:
221.0221
MDL Number:
MFCD01705455
SMILES:
ClCCNP(=O)(NCCCl)O
NSC Number:
297900
Properties
Properties
 
Form:
Solid  
MP:
106-107℃  
Storage:
-20 ℃;  

Computed Properties
 
Complexity:
134  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
6  
XLogP3:
-0.4  

Downstream Synthesis Route
31645-39-3    39070-14-9   
(2-chloroethyl)((2-chloroethyl)amino(2-nitro-3-methylimidazol-4-yl)methoxyphosphoryl})amine 

[1]JournalofMedicinalChemistry,2008,vol.51,p.2412-2420

[2]Patent:WO2007/2931,2007,A2.Locationinpatent:Page/Pagecolumn76;124-125

[1]Actapoloniaepharmaceutica,2013,vol.70,p.481-487

[1]Actapoloniaepharmaceutica,2013,vol.70,p.481-487

Literature

Title: Pharmacokinetics of TH-302: a hypoxically activated prodrug of bromo-isophosphoramide mustard in mice, rats, dogs and monkeys.

Journal: Cancer chemotherapy and pharmacology 20120301

Title: Anticancer activity of stabilized palifosfamide in vivo: schedule effects, oral bioavailability, and enhanced activity with docetaxel and doxorubicin.

Journal: Anti-cancer drugs 20120201

Title: The effect of N-acetylcysteine on the antitumor activity of ifosfamide.

Journal: Canadian journal of physiology and pharmacology 20110501

Title: Ifosfamide metabolites CAA, 4-OH-Ifo and Ifo-mustard reduce apical phosphate transport by changing NaPi-IIa in OK cells.

Journal: Kidney international 20061101

Title: [Identification of glufosfamide metabolites in rats].

Journal: Yao xue xue bao = Acta pharmaceutica Sinica 20060601

Title: Comparative preclinical toxicology and pharmacology of isophosphoramide mustard, the active metabolite of ifosfamide.

Journal: Cancer chemotherapy and pharmacology 20050201

Title: 1,3- vs 1,5-intramolecular alkylation reactions in isophosphoramide and phosphoramide mustards.

Journal: Chemical research in toxicology 20040901

Title: Phosphate prodrugs of isophosphoramide mustard.

Journal: Acta poloniae pharmaceutica 20030101

Title: Isophosphoramide mustard analogues as prodrugs for anticancer gene-directed enzyme-prodrug therapy (GDEPT).

Journal: Acta biochimica Polonica 20020101

Title: Mechanisms of resistance against cyclophosphamide and ifosfamide: can they be overcome without sacrificing selectivity?

Journal: Cancer treatment and research 20020101

Title: Identification of new aqueous chemical degradation products of isophosphoramide mustard.

Journal: Journal of pharmaceutical and biomedical analysis 20010601

Title: Prevention of isophosphamide-induced urothelial toxicity with 2-mercaptoethane sulphonate sodium (mesnum) in patients with advanced carcinoma.

Journal: Lancet (London, England) 19800927

Title: Hingorani P, et al. Preclinical activity of palifosfamide lysine (ZIO-201) in pediatric sarcomas including oxazaphosphorine-resistant osteosarcoma. Cancer Chemother Pharmacol. 2009 Sep;64(4):733-40.

Title: Jones B, et al. Anticancer activity of stabilized palifosfamide in vivo: schedule effects, oral bioavailability, and enhanced activity with docetaxel and doxorubicin. Anticancer Drugs. 2012 Feb;23(2):173-84.

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