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Pyridone 6

CAS No.:
457081-03-7
Catalog Number:
AG00DAQP
Molecular Formula:
C18H16FN3O
Molecular Weight:
309.3375
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
≥98%
1 week
United States
$169
- +
5mg
≥98%
1 week
United States
$218
- +
10mg
≥98%
1 week
United States
$298
- +
50mg
98%
1 week
United States
$1371
- +
100mg
98%
1 week
United States
$2390
- +
Product Description
Catalog Number:
AG00DAQP
Chemical Name:
Pyridone 6
CAS Number:
457081-03-7
Molecular Formula:
C18H16FN3O
Molecular Weight:
309.3375
MDL Number:
MFCD17019334
IUPAC Name:
4-tert-butyl-15-fluoro-3,5,10-triazatetracyclo[11.4.0.02,6.07,12]heptadeca-1(13),2(6),4,7(12),8,14,16-heptaen-11-one
InChI:
InChI=1S/C18H16FN3O/c1-18(2,3)17-21-14-10-5-4-9(19)8-12(10)13-11(15(14)22-17)6-7-20-16(13)23/h4-8H,1-3H3,(H,20,23)(H,21,22)
InChI Key:
VNDWQCSOSCCWIP-UHFFFAOYSA-N
SMILES:
Fc1ccc2c(c1)c1c(=O)[nH]ccc1c1c2[nH]c(n1)C(C)(C)C
UNII:
LDX3F0CCST
Properties
Complexity:
529  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
309.128g/mol
Formal Charge:
0
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
309.344g/mol
Monoisotopic Mass:
309.128g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
57.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4  
Literature
Title Journal
Structure and mechanism of action of the hydroxy-aryl-aldehyde class of IRE1 endoribonuclease inhibitors. Nature communications 20140828
Synephrine inhibits eotaxin-1 expression via the STAT6 signaling pathway. Molecules (Basel, Switzerland) 20140808
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery. The Biochemical journal 20130415
STAT6 phosphorylation inhibitors block eotaxin-3 secretion in bronchial epithelial cells. Bioorganic & medicinal chemistry 20120115
Pyridone 6, a pan-JAK inhibitor, ameliorates allergic skin inflammation of NC/Nga mice via suppression of Th2 and enhancement of Th17. Journal of immunology (Baltimore, Md. : 1950) 20111101
Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity. Nature biotechnology 20111101
Effects of a Janus kinase inhibitor, pyridone 6, on airway responses in a murine model of asthma. Biochemical and biophysical research communications 20110107
CP690,550 inhibits oncostatin M-induced JAK/STAT signaling pathway in rheumatoid synoviocytes. Arthritis research & therapy 20110101
Prolactin-induced Jak2 phosphorylation of RUSH: a key element in Jak/RUSH signaling. Molecular and cellular endocrinology 20100830
Structural and thermodynamic characterization of the TYK2 and JAK3 kinase domains in complex with CP-690550 and CMP-6. Journal of molecular biology 20100716
Non-cell-autonomous stimulation of stem cell proliferation following ablation of Tcf3. Experimental cell research 20100401
STAT3 signalling pathway is involved in the activation of microglia induced by 2.45 GHz electromagnetic fields. International journal of radiation biology 20100101
Dissecting specificity in the Janus kinases: the structures of JAK-specific inhibitors complexed to the JAK1 and JAK2 protein tyrosine kinase domains. Journal of molecular biology 20090320
Pyridone 6, a pan-Janus-activated kinase inhibitor, suppresses osteoclast formation and bone resorption through down-regulation of receptor activator of nuclear factor-kappaB (NF-kappaB) ligand (RANKL)-induced c-Fos and nuclear factor of activated T cells (NFAT) c1 expression. Biological & pharmaceutical bulletin 20090101
Virtual screening to successfully identify novel janus kinase 3 inhibitors: a sequential focused screening approach. Journal of medicinal chemistry 20081113
Chemotherapy-induced toxic erythema under treatment with pegylated liposomal doxorubicin: No restriction to palms and soles. Journal of the American Academy of Dermatology 20080201
Tissue factor/FVIIa activates Bcl-2 and prevents doxorubicin-induced apoptosis in neuroblastoma cells. BMC cancer 20080101
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Proceedings of the National Academy of Sciences of the United States of America 20071218
Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors. Bioorganic & medicinal chemistry letters 20071215
Pyridone 6, a pan-Janus-activated kinase inhibitor, induces growth inhibition of multiple myeloma cells. Cancer research 20061001
IL-4 induced MUC4 enhancement in respiratory epithelial cells in vitro is mediated through JAK-3 selective signaling. Respiratory research 20060101
Tumor necrosis factor-alpha differentially regulates the expression of proinflammatory genes in human airway smooth muscle cells by activation of interferon-beta-dependent CD38 pathway. Molecular pharmacology 20040801
Photochemical preparation of a pyridone containing tetracycle: a Jak protein kinase inhibitor. Bioorganic & medicinal chemistry letters 20020422
Properties