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935888-69-0,MFCD25976563
Catalog No.:AA00GU2D

935888-69-0 | ONX-0912

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$24.00   $17.00
- +
5mg
98%
in stock  
$57.00   $40.00
- +
10mg
98%
in stock  
$85.00   $60.00
- +
25mg
98%
in stock  
$143.00   $100.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00GU2D
Chemical Name:
ONX-0912
CAS Number:
935888-69-0
Molecular Formula:
C25H32N4O7S
Molecular Weight:
532.6092
MDL Number:
MFCD25976563
SMILES:
COC[C@@H](C(=O)N[C@H](C(=O)[C@]1(C)OC1)Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1cnc(s1)C)COC
Properties
Computed Properties
 
Complexity:
825  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Heavy Atom Count:
37  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
14  
XLogP3:
1.1  

Literature

Title: Molecular mechanisms of acquired proteasome inhibitor resistance.

Journal: Journal of medicinal chemistry 20121213

Title: Carfilzomib and ONX 0912 inhibit cell survival and tumor growth of head and neck cancer and their activities are enhanced by suppression of Mcl-1 or autophagy.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20121015

Title: Inactivating PSMB5 mutations and P-glycoprotein (multidrug resistance-associated protein/ATP-binding cassette B1) mediate resistance to proteasome inhibitors: ex vivo efficacy of (immuno)proteasome inhibitors in mononuclear blood cells from patients with rheumatoid arthritis.

Journal: The Journal of pharmacology and experimental therapeutics 20120401

Title: Drugs: More shots on target.

Journal: Nature 20111214

Title: Novel proteasome inhibitors to overcome bortezomib resistance.

Journal: Journal of the National Cancer Institute 20110706

Title: A novel orally active proteasome inhibitor ONX 0912 triggers in vitro and in vivo cytotoxicity in multiple myeloma.

Journal: Blood 20101202

Title: Design and synthesis of an orally bioavailable and selective peptide epoxyketone proteasome inhibitor (PR-047).

Journal: Journal of medicinal chemistry 20090514

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