Catalog No.:AA01EAYK

890128-81-1 | BFH772

Name: Name:BFH772
Brand: AABLOCKS
SKU: AA01EAYK
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1mg

98%

in stock

$11.00 $8.00

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5mg

98%

in stock

$33.00 $23.00

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25mg

98%

in stock

$85.00 $60.00

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50mg

98%

in stock

$134.00 $94.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Download SDS

Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA01EAYK

Chemical Name:

BFH772

CAS Number:

890128-81-1

Molecular Formula:

C23H16F3N3O3

Molecular Weight:

439.3866

MDL Number:

MFCD30534392

SMILES:

OCc1ncnc(c1)Oc1ccc2c(c1)cccc2C(=O)Nc1cccc(c1)C(F)(F)F

Properties

Computed Properties

Complexity:

635

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

4.2

Downstream Synthesis Route

890128-75-3

CASUnavailable

890128-81-1

[1]CurrentPatentAssignee:NOVARTISAG;Novartis(w/oSandoz)-WO2007/31265,2007,A2Locationinpatent:Page/Pagecolumn39

[2]CurrentPatentAssignee:Novartis(w/oSandoz);NOVARTISAG-WO2006/59234,2006,A2Locationinpatent:Page/Pagecolumn63

890128-81-1

890128-82-2

[1]CurrentPatentAssignee:NOVARTISAG;Novartis(w/oSandoz)-WO2007/31265,2007,A2Locationinpatent:Page/Pagecolumn40

[2]CurrentPatentAssignee:Novartis(w/oSandoz);NOVARTISAG-WO2006/59234,2006,A2Locationinpatent:Page/Pagecolumn63

890128-71-9

890128-81-1

[1]Bold,Guido;Schnell,Christian;Furet,Pascal;McSheehy,Paul;Brüggen,Josef;Mestan,Jürgen;Manley,PaulW.;Drückes,Peter;Burglin,Marion;Dürler,Ursula;Loretan,Jacqueline;Reuter,Robert;Wartmann,Markus;Theuer,Andreas;Bauer-Probst,Beatrice;Martiny-Baron,Georg;Allegrini,Peter;Goepfert,Arnaud;Wood,Jeanette;Littlewood-Evans,Amanda[JournalofMedicinalChemistry,2016,vol.59,#1,p.132-146]

890128-75-3

890128-81-1

2437-17-4

6-(6-hydroxymethylpyrimidin-4-yloxy)naphthalene-1-carboxylicacid(3-trifluoromethylphenyl)amide

[1]JournalofMedicinalChemistry,2016,vol.59,p.132-146

Literature

Title: Bold G, et al. A Novel Potent Oral Series of VEGFR2 Inhibitors Abrogate Tumor Growth by Inhibiting Angiogenesis. J Med Chem. 2016 Jan 14;59(1):132-46.

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SDS