Home Other Building Blocks 1300031-49-5
1300031-49-5,MFCD22124472
Catalog No.:AA000TTH

1300031-49-5 | I-Bet151

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$52.00   $36.00
- +
5mg
≥98%
in stock  
$140.00   $98.00
- +
10mg
98%
in stock  
$234.00   $164.00
- +
25mg
≥98%
in stock  
$575.00   $402.00
- +
50mg
98%
in stock  
$764.00   $535.00
- +
100mg
98%
in stock  
$1,300.00   $910.00
- +
500mg
99% (HPLC)
in stock  
$5,515.00   $3,861.00
- +
1000mg
99% (HPLC)
in stock  
$8,787.00   $6,151.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA000TTH
Chemical Name:
I-Bet151
CAS Number:
1300031-49-5
Molecular Formula:
C23H21N5O3
Molecular Weight:
415.4445
MDL Number:
MFCD22124472
SMILES:
COc1cc2c(cc1c1c(C)noc1C)ncc1c2n(c(=O)[nH]1)[C@@H](c1ccccn1)C
Properties
Computed Properties
 
Complexity:
665  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
31  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
2.7  

Literature

Title: The BET inhibitor JQ1 selectively impairs tumour response to hypoxia and downregulates CA9 and angiogenesis in triple negative breast cancer.

Journal: Oncogene 20170105

Title: Antimyeloma activity of bromodomain inhibitors on the human myeloma cell line U266 by downregulation of MYCL.

Journal: Anti-cancer drugs 20160901

Title: Bromodomain and extraterminal (BET) proteins regulate biliary-driven liver regeneration.

Journal: Journal of hepatology 20160201

Title: BET Bromodomain Inhibition as a Therapeutic Strategy in Ovarian Cancer by Downregulating FoxM1.

Journal: Theranostics 20160101

Title: BRD4 is a novel therapeutic target for liver fibrosis.

Journal: Proceedings of the National Academy of Sciences of the United States of America 20151222

Title: Synergistic activity of BET protein antagonist-based combinations in mantle cell lymphoma cells sensitive or resistant to ibrutinib.

Journal: Blood 20150924

Title: BET bromodomain inhibition suppresses graft-versus-host disease after allogeneic bone marrow transplantation in mice.

Journal: Blood 20150423

Title: GLI2-dependent c-MYC upregulation mediates resistance of pancreatic cancer cells to the BET bromodomain inhibitor JQ1.

Journal: Scientific reports 20150101

Title: Blockade of oncogenic IκB kinase activity in diffuse large B-cell lymphoma by bromodomain and extraterminal domain protein inhibitors.

Journal: Proceedings of the National Academy of Sciences of the United States of America 20140805

Title: Histone deacetylase 2 and N-Myc reduce p53 protein phosphorylation at serine 46 by repressing gene transcription of tumor protein 53-induced nuclear protein 1.

Journal: Oncotarget 20140601

Title: Targeting Myc in KSHV-associated primary effusion lymphoma with BET bromodomain inhibitors.

Journal: Oncogene 20140529

Title: Potent antimyeloma activity of the novel bromodomain inhibitors I-BET151 and I-BET762.

Journal: Blood 20140130

Title: Discovery, Design, and Optimization of Isoxazole Azepine BET Inhibitors.

Journal: ACS medicinal chemistry letters 20130912

Title: Optimization of 3,5-dimethylisoxazole derivatives as potent bromodomain ligands.

Journal: Journal of medicinal chemistry 20130425

Title: From ApoA1 upregulation to BET family bromodomain inhibition: discovery of I-BET151.

Journal: Bioorganic & medicinal chemistry letters 20120415

Title: Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamides.

Journal: Journal of medicinal chemistry 20120126

Title: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia.

Journal: Nature 20111002

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