1035270-39-3,MFCD22580423
Catalog No.:AA008TAZ

1035270-39-3 | Azd4547

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$7.00   $5.00
- +
5mg
98%
in stock  
$15.00   $11.00
- +
10mg
98%
in stock  
$23.00   $16.00
- +
250mg
98%
in stock  
$182.00   $128.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA008TAZ
Chemical Name:
Azd4547
CAS Number:
1035270-39-3
Molecular Formula:
C26H33N5O3
Molecular Weight:
463.5719
MDL Number:
MFCD22580423
SMILES:
COc1cc(CCc2[nH]nc(c2)NC(=O)c2ccc(cc2)N2C[C@H](C)N[C@@H](C2)C)cc(c1)OC
Properties
Computed Properties
 
Complexity:
622  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
34  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
8  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.9  

Downstream Synthesis Route
24566-79-8    1035270-39-3   
N-(5-(3,5-dimethoxyphenethyl)-1H-pyrazol-3-yl)-4-((3S,5R)-4-(6-(1,3-dioxoisoindolin-2-yl)hexyl)-3,5-dimethylpiperazin-1-yl)benzamide 

[1]InternationalJournalofNanomedicine,2017,vol.12,p.5345-5357

1035270-39-3   
2-(14-bromo-3,6,9,9,12-tetraoxatetradecyl)isoindoline-1,3-dione 
 
C44H56N6O9 

[1]Patent:KR101820381,2018,B1.Locationinpatent:Paragraph0067-0069

[1]Patent:CN111072638,2020,A

[1]CurrentPatentAssignee:ABBISKOTHERAPEUTICSCO.,LTD.;WUXIHEYUBIOMEDICALTECH-CN115819239,2023,ALocationinpatent:Paragraph0088;0166-0170

Literature

Title: Design, synthesis and biological evaluation of novel FGFR inhibitors bearing an indazole scaffold.

Journal: Organic & biomolecular chemistry 20150728

Title: Transforming fusions of FGFR and TACC genes in human glioblastoma.

Journal: Science (New York, N.Y.) 20120907

Title: AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family.

Journal: Cancer research 20120415

Title: Gavine PR, et al. AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family. Cancer Res, 2012, 72(8), 2045-2056.

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SDS
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Tags:1035270-39-3 Molecular Formula|1035270-39-3 MDL|1035270-39-3 SMILES|1035270-39-3 Azd4547
Catalog No.: AA008TAZ
1035270-39-3,MFCD22580423
1035270-39-3 | Azd4547
Pack Size: 1mg
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 5mg
Purity: 98%
in stock
$15.00 $11.00
Pack Size: 10mg
Purity: 98%
in stock
$23.00 $16.00
Pack Size: 250mg
Purity: 98%
in stock
$182.00 $128.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA008TAZ
Chemical Name: Azd4547
CAS Number: 1035270-39-3
Molecular Formula: C26H33N5O3
Molecular Weight: 463.5719
MDL Number: MFCD22580423
SMILES: COc1cc(CCc2[nH]nc(c2)NC(=O)c2ccc(cc2)N2C[C@H](C)N[C@@H](C2)C)cc(c1)OC
Properties
Complexity: 622  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 34  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 8  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.9  
Downstream Synthesis Route
24566-79-8    1035270-39-3   
N-(5-(3,5-dimethoxyphenethyl)-1H-pyrazol-3-yl)-4-((3S,5R)-4-(6-(1,3-dioxoisoindolin-2-yl)hexyl)-3,5-dimethylpiperazin-1-yl)benzamide 

[1]InternationalJournalofNanomedicine,2017,vol.12,p.5345-5357

1035270-39-3   
2-(14-bromo-3,6,9,9,12-tetraoxatetradecyl)isoindoline-1,3-dione 
 
C44H56N6O9 

[1]Patent:KR101820381,2018,B1.Locationinpatent:Paragraph0067-0069

20767-04-8    1035270-39-3 

[1]Patent:CN111072638,2020,A

234082-05-4    2615357-33-8    1035270-39-3 

[1]CurrentPatentAssignee:ABBISKOTHERAPEUTICSCO.,LTD.;WUXIHEYUBIOMEDICALTECH-CN115819239,2023,ALocationinpatent:Paragraph0088;0166-0170

Literature fold

Title: Design, synthesis and biological evaluation of novel FGFR inhibitors bearing an indazole scaffold.

Journal: Organic & biomolecular chemistry20150728

Title: Transforming fusions of FGFR and TACC genes in human glioblastoma.

Journal: Science (New York, N.Y.)20120907

Title: AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family.

Journal: Cancer research20120415

Title: Gavine PR, et al. AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family. Cancer Res, 2012, 72(8), 2045-2056.

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