Home Quinolines 700874-72-2
700874-72-2,MFCD12923319
Catalog No.:AA0033PR

700874-72-2 | 4-[2-(6-Methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
98%
in stock  
$14.00   $10.00
- +
10mg
98%
in stock  
$21.00   $15.00
- +
25mg
98%
in stock  
$33.00   $23.00
- +
  • Technical Information
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA0033PR
Chemical Name:
4-[2-(6-Methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide
CAS Number:
700874-72-2
Molecular Formula:
C22H19N5O
Molecular Weight:
369.4192
MDL Number:
MFCD12923319
SMILES:
Cc1cccc(n1)c1nn2c(c1c1ccnc3c1cc(cc3)C(=O)N)CCC2
Properties
Properties
 
BP:
619°C at 760 mmHg  
Form:
Solid  
MP:
241-242°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
585  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.4  

Literature

Title: Prenatal nicotine exposure intergenerationally programs imperfect articular cartilage via histone deacetylation through maternal lineage.

Journal: Toxicology and applied pharmacology 20180801

Title: Galunisertib modifies the liver fibrotic composition in the Abcb4Ko mouse model.

Journal: Archives of toxicology 20180701

Title: Preclinical assessment of galunisertib (LY2157299 monohydrate), a first-in-class transforming growth factor-β receptor type I inhibitor.

Journal: Oncotarget 20180123

Title: Discovery of N-((4-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(6-methylpyridin-2-yl)-1H-imidazol-2-yl)methyl)-2-fluoroaniline (EW-7197): a highly potent, selective, and orally bioavailable inhibitor of TGF-β type I receptor kinase as cancer immunotherapeutic/antifibrotic agent.

Journal: Journal of medicinal chemistry 20140522

Title: Optimization of a dihydropyrrolopyrazole series of transforming growth factor-beta type I receptor kinase domain inhibitors: discovery of an orally bioavailable transforming growth factor-beta receptor type I inhibitor as antitumor agent.

Journal: Journal of medicinal chemistry 20080410

Title: Cong L, et al. Targeting the TGF-β receptor with kinase inhibitors for scleroderma therapy. Arch Pharm (Weinheim). 2014 Sep;347(9):609-15.

Title: Serova M, et al. Effects of TGF-beta signalling inhibition with galunisertib (LY2157299) in hepatocellular carcinoma models and in ex vivo whole tumor tissue samples from patients. Oncotarget. 2015 Aug 28;6(25):21614-27

Title: Bueno L, et al. Semi-mechanistic modelling of the tumour growth inhibitory effects of LY2157299, a new type I receptor TGF-beta kinase antagonist, in mice. Eur J Cancer. 2008 Jan;44(1):142-50.

Title: Herbertz S, et al. Clinical development of galunisertib (LY2157299 monohydrate), a small molecule inhibitor of transforming growth factor-beta signaling pathway. Drug Des Devel Ther. 2015 Aug 10;9:4479-99.

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SDS
Tags:700874-72-2 Molecular Formula|700874-72-2 MDL|700874-72-2 SMILES|700874-72-2 4-[2-(6-Methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide