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936563-87-0,MFCD12032093
Catalog No.:AA00GU2I

936563-87-0 | PCI-32765 Racemate

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Purity
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5mg
95%
1 week  
$146.00   $102.00
- +
10mg
95%
1 week  
$203.00   $142.00
- +
50mg
95%
1 week  
$431.00   $302.00
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100mg
95%
1 week  
$698.00   $489.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00GU2I
Chemical Name:
PCI-32765 Racemate
CAS Number:
936563-87-0
Molecular Formula:
C25H24N6O2
Molecular Weight:
440.4971
MDL Number:
MFCD12032093
SMILES:
C=CC(=O)N1CCCC(C1)n1nc(c2c1ncnc2N)c1ccc(cc1)Oc1ccccc1
Properties
Computed Properties
 
Complexity:
678  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
33  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
1  
XLogP3:
3.6  

Literature

Title: Promising efficacy of novel BTK inhibitor AC0010 in mantle cell lymphoma.

Journal: Journal of cancer research and clinical oncology 20180401

Title: Bruton's tyrosine kinase inhibitors: first and second generation agents for patients with Chronic Lymphocytic Leukemia (CLL).

Journal: Expert opinion on investigational drugs 20180101

Title: The Phospholipase Cγ2 Mutants R665W and L845F Identified in Ibrutinib-resistant Chronic Lymphocytic Leukemia Patients Are Hypersensitive to the Rho GTPase Rac2 Protein.

Journal: The Journal of biological chemistry 20161014

Title: Bromodomain inhibitor OTX015 (MK-8628) combined with targeted agents shows strong in vivo antitumor activity in lymphoma.

Journal: Oncotarget 20160906

Title: Mantle Cell Lymphoma.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20160410

Title: Label-Free Bottom-Up Proteomic Workflow for Simultaneously Assessing the Target Specificity of Covalent Drug Candidates and Their Off-Target Reactivity to Selected Proteins.

Journal: Chemical research in toxicology 20160119

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

Journal: Blood 20150924

Title: Ibrutinib: a review of its use in patients with mantle cell lymphoma or chronic lymphocytic leukaemia.

Journal: Drugs 20150501

Title: Ibrutinib in pretreated Waldenström's macroglobulinaemia.

Journal: The Lancet. Oncology 20150501

Title: Functional characterization of BTK(C481S) mutation that confers ibrutinib resistance: exploration of alternative kinase inhibitors.

Journal: Leukemia 20150401

Title: Absorption, metabolism, and excretion of oral ¹⁴C radiolabeled ibrutinib: an open-label, phase I, single-dose study in healthy men.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20150201

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: Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765).

Journal: Leukemia & lymphoma 20131101

Title: Ibrutinib: a novel Bruton's tyrosine kinase inhibitor with outstanding responses in patients with chronic lymphocytic leukemia.

Journal: Leukemia & lymphoma 20130801

Title: Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia.

Journal: The New England journal of medicine 20130704

Title: Ibrutinib: a strong candidate for the future of mantle cell lymphoma treatment.

Journal: Expert review of clinical immunology 20130601

Title: Ibrutinib (PCI-32765), the first BTK (Bruton's tyrosine kinase) inhibitor in clinical trials.

Journal: Current hematologic malignancy reports 20130301

Title: Ibrutinib and novel BTK inhibitors in clinical development.

Journal: Journal of hematology & oncology 20130101

Title: Inhibitors of B-cell receptor signaling for patients with B-cell malignancies.

Journal: Cancer journal (Sudbury, Mass.) 20120901

Title: Bruton tyrosine kinase inhibition is a novel therapeutic strategy targeting tumor in the bone marrow microenvironment in multiple myeloma.

Journal: Blood 20120830

Title: Exploiting synthetic lethality for the therapy of ABC diffuse large B cell lymphoma.

Journal: Cancer cell 20120612

Title: The clinically active BTK inhibitor PCI-32765 targets B-cell receptor- and chemokine-controlled adhesion and migration in chronic lymphocytic leukemia.

Journal: Blood 20120315

Title: Inhibiting B-cell receptor signaling pathways in chronic lymphocytic leukemia.

Journal: Current hematologic malignancy reports 20120301

Title: Novel targeted therapies for mantle cell lymphoma.

Journal: Oncotarget 20120201

Title: Modeling pharmacological inhibition of mast cell degranulation as a therapy for insulinoma.

Journal: Neoplasia (New York, N.Y.) 20111101

Title: Bruton tyrosine kinase represents a promising therapeutic target for treatment of chronic lymphocytic leukemia and is effectively targeted by PCI-32765.

Journal: Blood 20110609

Title: Inhibition of IgE-mediated secretion from human basophils with a highly selective Bruton's tyrosine kinase, Btk, inhibitor.

Journal: International immunopharmacology 20110401

Title: The Bruton tyrosine kinase inhibitor PCI-32765 ameliorates autoimmune arthritis by inhibition of multiple effector cells.

Journal: Arthritis research & therapy 20110101

Title: More than just B-cell inhibition.

Journal: Arthritis research & therapy 20110101

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