252003-65-9,MFCD07772279
Catalog No.:AA002QST

252003-65-9 | 4-Isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-[[[[4-(1-pyrrolidinyl)butyl]amino]carbonyl]amino]-

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$153.00   $107.00
- +
10mg
95%
in stock  
$300.00   $210.00
- +
25mg
95%
in stock  
$601.00   $421.00
- +
50mg
95%
in stock  
$1,001.00   $701.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002QST
Chemical Name:
4-Isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-[[[[4-(1-pyrrolidinyl)butyl]amino]carbonyl]amino]-
CAS Number:
252003-65-9
Molecular Formula:
C20H24BrF2N5O3S
Molecular Weight:
532.4021
MDL Number:
MFCD07772279
SMILES:
O=C(Nc1snc(c1C(=O)N)OCc1c(F)cc(cc1F)Br)NCCCCN1CCCC1
Properties
Properties
 
BP:
548.601°C at 760 mmHg  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
622  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
32  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
10  
XLogP3:
3.7  

Literature

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

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Vascular endothelial growth factor (VEGF) receptors: drugs and new inhibitors.

Journal: Journal of medicinal chemistry 20121227

Title: Discovery of imidazole vinyl pyrimidines as a novel class of kinase inhibitors which inhibit Tie-2 and are orally bioavailable.

Journal: Bioorganic & medicinal chemistry letters 20080815

Title: Design and synthesis of dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole oximes as potent dual inhibitors of TIE-2 and VEGF-R2 receptor tyrosine kinases.

Journal: Bioorganic & medicinal chemistry letters 20080315

Title: A phase I/randomized phase II, non-comparative, multicenter, open label trial of CP-547,632 in combination with paclitaxel and carboplatin or paclitaxel and carboplatin alone as first-line treatment for advanced non-small cell lung cancer (NSCLC).

Journal: Cancer chemotherapy and pharmacology 20070601

Title: Pharmacological characterization of CP-547,632, a novel vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for cancer therapy.

Journal: Cancer research 20031101

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SDS
Related Products of 252003-65-9
Tags:252003-65-9 Molecular Formula|252003-65-9 MDL|252003-65-9 SMILES|252003-65-9 4-Isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-[[[[4-(1-pyrrolidinyl)butyl]amino]carbonyl]amino]-
Catalog No.: AA002QST
252003-65-9,MFCD07772279
252003-65-9 | 4-Isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-[[[[4-(1-pyrrolidinyl)butyl]amino]carbonyl]amino]-
Pack Size: 1mg
Purity: ≥98%
in stock
$153.00 $107.00
Pack Size: 10mg
Purity: 95%
in stock
$300.00 $210.00
Pack Size: 25mg
Purity: 95%
in stock
$601.00 $421.00
Pack Size: 50mg
Purity: 95%
in stock
$1,001.00 $701.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA002QST
Chemical Name: 4-Isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-[[[[4-(1-pyrrolidinyl)butyl]amino]carbonyl]amino]-
CAS Number: 252003-65-9
Molecular Formula: C20H24BrF2N5O3S
Molecular Weight: 532.4021
MDL Number: MFCD07772279
SMILES: O=C(Nc1snc(c1C(=O)N)OCc1c(F)cc(cc1F)Br)NCCCCN1CCCC1
Properties
BP: 548.601°C at 760 mmHg  
Storage: Keep in dry area;2-8℃;  
Complexity: 622  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 32  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 10  
XLogP3: 3.7  
Literature fold

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

Journal: Bioorganic & medicinal chemistry letters20130801

Title: Vascular endothelial growth factor (VEGF) receptors: drugs and new inhibitors.

Journal: Journal of medicinal chemistry20121227

Title: Discovery of imidazole vinyl pyrimidines as a novel class of kinase inhibitors which inhibit Tie-2 and are orally bioavailable.

Journal: Bioorganic & medicinal chemistry letters20080815

Title: Design and synthesis of dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole oximes as potent dual inhibitors of TIE-2 and VEGF-R2 receptor tyrosine kinases.

Journal: Bioorganic & medicinal chemistry letters20080315

Title: A phase I/randomized phase II, non-comparative, multicenter, open label trial of CP-547,632 in combination with paclitaxel and carboplatin or paclitaxel and carboplatin alone as first-line treatment for advanced non-small cell lung cancer (NSCLC).

Journal: Cancer chemotherapy and pharmacology20070601

Title: Pharmacological characterization of CP-547,632, a novel vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for cancer therapy.

Journal: Cancer research20031101

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