Home Other Building Blocks 796967-16-3
796967-16-3,MFCD11840918
Catalog No.:AA0036F1

796967-16-3 | Linifanib

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98+%
in stock  
$11.00   $8.00
- +
5mg
98+%
in stock  
$23.00   $16.00
- +
50mg
98+%
in stock  
$91.00   $64.00
- +
250mg
98+%
in stock  
$260.00   $182.00
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  • Technical Information
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA0036F1
Chemical Name:
Linifanib
CAS Number:
796967-16-3
Molecular Formula:
C21H18FN5O
Molecular Weight:
375.3989
MDL Number:
MFCD11840918
SMILES:
O=C(Nc1cc(C)ccc1F)Nc1ccc(cc1)c1cccc2c1c(N)n[nH]2
Properties
Properties
 
BP:
542.203 °C at 760 mmHg  
Form:
Solid  
MP:
180-183 °C (dec.);  
Storage:
2-8℃;  

Computed Properties
 
Complexity:
541  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
3  
XLogP3:
3.9  

Literature

Title: A selective chemical probe for exploring the role of CDK8 and CDK19 in human disease.

Journal: Nature chemical biology 20151201

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Phase 1 trial of linifanib (ABT-869) in patients with refractory or relapsed acute myeloid leukemia.

Journal: Leukemia & lymphoma 20120801

Title: 3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3).

Journal: Bioorganic & medicinal chemistry letters 20120715

Title: FDG-PET as a pharmacodynamic biomarker for early assessment of treatment response to linifanib (ABT-869) in a non-small cell lung cancer xenograft model.

Journal: Cancer chemotherapy and pharmacology 20120601

Title: An open-label, phase 1 study evaluating safety, tolerability, and pharmacokinetics of linifanib (ABT-869) in Japanese patients with solid tumors.

Journal: Cancer chemotherapy and pharmacology 20120601

Title: A novel multi-targeted tyrosine kinase inhibitor, linifanib (ABT-869), produces functional and structural changes in tumor vasculature in an orthotopic rat glioma model.

Journal: Cancer chemotherapy and pharmacology 20120401

Title: BPR1J-097, a novel FLT3 kinase inhibitor, exerts potent inhibitory activity against AML.

Journal: British journal of cancer 20120131

Title: Phase 2 trial of linifanib (ABT-869) in patients with advanced renal cell cancer after sunitinib failure.

Journal: European journal of cancer (Oxford, England : 1990) 20111201

Title: A comparative study of dynamic contrast-enhanced MRI parameters as biomarkers for anti-angiogenic drug therapy.

Journal: NMR in biomedicine 20111101

Title: Comprehensive analysis of kinase inhibitor selectivity.

Journal: Nature biotechnology 20111030

Title: Phase 2 trial of Linifanib (ABT-869) in patients with advanced non-small cell lung cancer.

Journal: Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 20110801

Title: Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3).

Journal: Bioorganic & medicinal chemistry 20110715

Title: ABT-869, a multitargeted receptor tyrosine kinase inhibitor, reduces tumor microvascularity and improves vascular wall integrity in preclinical tumor models.

Journal: The Journal of pharmacology and experimental therapeutics 20110701

Title: Discovery, synthesis, and investigation of the antitumor activity of novel piperazinylpyrimidine derivatives.

Journal: European journal of medicinal chemistry 20110601

Title: The multitargeted receptor tyrosine kinase inhibitor linifanib (ABT-869) induces apoptosis through an Akt and glycogen synthase kinase 3β-dependent pathway.

Journal: Molecular cancer therapeutics 20110601

Title: Activation state-dependent binding of small molecule kinase inhibitors: structural insights from biochemistry.

Journal: Chemistry & biology 20101124

Title: Antiangiogenic agents in advanced gastrointestinal malignancies: past, present and a novel future.

Journal: Oncotarget 20101101

Title: Linifanib.

Journal: Drugs in R&D 20100701

Title: ABT-869 inhibits the proliferation of Ewing Sarcoma cells and suppresses platelet-derived growth factor receptor beta and c-KIT signaling pathways.

Journal: Molecular cancer therapeutics 20100301

Title: Three dimensional pharmacophore modelling for c-Kit receptor tyrosine kinase inhibitors.

Journal: European journal of medicinal chemistry 20100101

Title: Pulse-modulated second harmonic imaging microscope quantitatively demonstrates marked increase of collagen in tumor after chemotherapy.

Journal: Journal of biomedical optics 20100101

Title: Phase I and biomarker study of ABT-869, a multiple receptor tyrosine kinase inhibitor, in patients with refractory solid malignancies.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20091001

Title: Effect of the multitargeted receptor tyrosine kinase inhibitor, ABT-869 [N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea], on blood pressure in conscious rats and mice: reversal with antihypertensive agents and effect on tumor growth inhibition.

Journal: The Journal of pharmacology and experimental therapeutics 20090601

Title: Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML.

Journal: Blood 20090423

Title: ETA receptor blockade with atrasentan prevents hypertension with the multitargeted tyrosine kinase inhibitor ABT-869 in telemetry-instrumented rats.

Journal: Journal of cardiovascular pharmacology 20090201

Title: ABT-869, a promising multi-targeted tyrosine kinase inhibitor: from bench to bedside.

Journal: Journal of hematology & oncology 20090101

Title: Simultaneous determination of a hydrophobic drug candidate and its metabolite in human plasma with salting-out assisted liquid/liquid extraction using a mass spectrometry friendly salt.

Journal: Journal of pharmaceutical and biomedical analysis 20081201

Title: ABT-869, a multi-targeted tyrosine kinase inhibitor, in combination with rapamycin is effective for subcutaneous hepatocellular carcinoma xenograft.

Journal: Journal of hepatology 20081201

Title: 7-Aminopyrazolo[1,5-a]pyrimidines as potent multitargeted receptor tyrosine kinase inhibitors.

Journal: Journal of medicinal chemistry 20080710

Title: In vivo activity of ABT-869, a multi-target kinase inhibitor, against acute myeloid leukemia with wild-type FLT3 receptor.

Journal: Leukemia research 20080701

Title: 3-amino-benzo[d]isoxazoles as novel multitargeted inhibitors of receptor tyrosine kinases.

Journal: Journal of medicinal chemistry 20080313

Title: Synergistic antileukemic effects between ABT-869 and chemotherapy involve downregulation of cell cycle-regulated genes and c-Mos-mediated MAPK pathway.

Journal: Leukemia 20080101

Title: Identification of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted kinase inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20080101

Title: A quantitative analysis of kinase inhibitor selectivity.

Journal: Nature biotechnology 20080101

Title: ABT-869, a multitargeted receptor tyrosine kinase inhibitor: inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia.

Journal: Blood 20070415

Title: Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor.

Journal: Journal of medicinal chemistry 20070405

Title: Hypoxia-inducible factor-1 inhibition in combination with temozolomide treatment exhibits robust antitumor efficacy in vivo.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20060801

Title: Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor.

Journal: Molecular cancer therapeutics 20060401

Title: Inhibition of phosphorylation of the colony-stimulating factor-1 receptor (c-Fms) tyrosine kinase in transfected cells by ABT-869 and other tyrosine kinase inhibitors.

Journal: Molecular cancer therapeutics 20060401

Title: A high-throughput, fully automated liquid/liquid extraction liquid chromatography/mass spectrometry method for the quantitation of a new investigational drug ABT-869 and its metabolite A-849529 in human plasma samples.

Journal: Rapid communications in mass spectrometry : RCM 20060101

Title: A high-throughput liquid chromatography/tandem mass spectrometry method for simultaneous quantification of a hydrophobic drug candidate and its hydrophilic metabolite in human urine with a fully automated liquid/liquid extraction.

Journal: Rapid communications in mass spectrometry : RCM 20060101

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