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252979-56-9,MFCD19690955
Catalog No.:AA01E3US

252979-56-9 | BanoxantroneDihydrochloride

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5mg
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA01E3US
Chemical Name:
BanoxantroneDihydrochloride
CAS Number:
252979-56-9
Molecular Formula:
C22H30Cl2N4O6
Molecular Weight:
517.4028
MDL Number:
MFCD19690955
SMILES:
O=C1c2c(NCC[N+](C)(C)[O-])ccc(c2C(=O)c2c1c(O)ccc2O)NCC[N+](C)(C)[O-].Cl.Cl
Properties
Computed Properties
 
Complexity:
644  
Covalently-Bonded Unit Count:
3  
Heavy Atom Count:
34  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
6  
Rotatable Bond Count:
8  

Literature

Title: Cytochrome P450 2S1 is reduced by NADPH-cytochrome P450 reductase.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20110601

Title: Efficient hypoxic activation of the anticancer agent AQ4N by CYP2S1 and CYP2W1.

Journal: Molecular pharmacology 20100901

Title: Effects of cytokine-induced macrophages on the response of tumor cells to banoxantrone (AQ4N).

Journal: Molecular cancer therapeutics 20090501

Title: The hypoxia-activated ProDrug AQ4N penetrates deeply in tumor tissues and complements the limited distribution of mitoxantrone.

Journal: Cancer research 20090201

Title: Gene therapy approaches to enhance bioreductive drug treatment.

Journal: The British journal of radiology 20081001

Title: Evaluation of the antiangiogenic potential of AQ4N.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20080301

Title: Bioreductive drugs: from concept to clinic.

Journal: Clinical oncology (Royal College of Radiologists (Great Britain)) 20070801

Title: AQ4, an antitumor anthracenedione, inhibits endothelial cell proliferation and vascular endothelial growth factor secretion: implications for the therapy of ocular neovascular disorders.

Journal: European journal of pharmacology 20070730

Title: Selective tumor targeting by the hypoxia-activated prodrug AQ4N blocks tumor growth and metastasis in preclinical models of pancreatic cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20070401

Title: Examination of the distribution of the bioreductive drug AQ4N and its active metabolite AQ4 in solid tumours by imaging matrix-assisted laser desorption/ionisation mass spectrometry.

Journal: Rapid communications in mass spectrometry : RCM 20070101

Title: Tumor hypoxia in cancer therapy.

Journal: Methods in enzymology 20070101

Title: Hypoxia: targeting the tumour.

Journal: Anti-cancer agents in medicinal chemistry 20060701

Title: Radiation sensitization with redox modulators: a promising approach.

Journal: International journal of radiation oncology, biology, physics 20060201

Title: A cytochrome P450 2B6 meditated gene therapy strategy to enhance the effects of radiation or cyclophosphamide when combined with the bioreductive drug AQ4N.

Journal: The journal of gene medicine 20050701

Title: The chemopotentiation of cisplatin by the novel bioreductive drug AQ4N.

Journal: British journal of cancer 20010801

Title: A preclinical pharmacokinetic study of the bioreductive drug AQ4N.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20010401

Title: Enhancement of chemotherapy and radiotherapy of murine tumours by AQ4N, a bioreductively activated anti-tumour agent.

Journal: British journal of cancer 20000601

Title: Hejmadi MV, et al. DNA damage following combination of radiation with the bioreductive drug AQ4N: possible selective toxicity to oxic and hypoxic tumour cells. Br J Cancer. 1996 Feb;73(4):499-505.

Title: Manley E Jr, et al. Impact of tumor blood flow modulation on tumor sensitivity to the bioreductive drug banoxantrone. J Pharmacol Exp Ther. 2013 Feb;344(2):368-77.

Title: Williams KJ, et al. In vivo activation of the hypoxia-targeted cytotoxin AQ4N in human tumor xenografts. Mol Cancer Ther. 2009 Dec;8(12):3266-75.

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Tags:252979-56-9 Molecular Formula|252979-56-9 MDL|252979-56-9 SMILES|252979-56-9 BanoxantroneDihydrochloride