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MedKoo product information:
PKI-587
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MedKoo Code#: 202255
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Name: PKI-587
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CAS#: 1197160-78-3
Synonym:
Code name: PKI-587. CA Index Name: Urea, N-[4-[[4-(dimethylamino)-1-piperidinyl]carbonyl]phenyl]-N'-[4-(4,6-di-4-morpholinyl-1,3,5-triazin-2-yl)phenyl]-.
Other Names: 1-[4-[[4-(Dimethylamino)piperidin-1-yl]carbonyl]phenyl]-3-[4-[4,6-bis(morpholino)-1,3,5-triazin-2-yl]phenyl]urea.
IUPAC/Chemical name:
1-(4-(4-(dimethylamino)piperidine-1-carbonyl)phenyl)-3-(4-(4,6-dimorpholino-1,3,5-triazin-2-yl)phenyl)urea
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Chemical structure
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Theoretical analysis
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Chemical Formula: C32H41N9O4
Exact Mass: 615.32815
Molecular Weight: 615.72
m/z: 615.32815 (100.0%), 616.33151 (34.6%),
617.33486 (5.8%), 616.32519 (3.3%), 617.32854 (1.2%)
Elemental Analysis: C, 62.42; H, 6.71; N,
20.47; O, 10.39
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Availability and price:
PKI-587, 99%(HPLC), in stock.
To inquire quotation and lead time or to ask questions, please send email to
sales@medkoo.com to describe your needs. A representative
will respond your email shortly. We offer big discount for orders of bulk quantities.
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Information about this agent
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Dual PI3 Kinase/mTOR
Inhibitor PKI-587 is an agent targeting the
phosphatidylinositol 3 kinase (PI3K) and mammalian target of rapamycin (mTOR)
in the PI3K/mTOR signaling pathway, with potential antineoplastic
activity. Upon intravenous administration, PI3K/mTOR kinase inhibitor
PKI-587 inhibits both PI3K and mTOR kinases, which may result in
apoptosis and growth inhibition of cancer cells overexpressing PI3K/mTOR.
Activation of the PI3K/mTOR pathway promotes cell growth, survival, and
resistance to chemotherapy and radiotherapy; mTOR, a serine/threonine
kinase downstream of PI3K, may also be activated independent of PI3K.
Check for
active clinical trials or
closed clinical trials using this agent. (NCI
Thesaurus).
PKI-587 is a PI3K/mTOR inhibitor, currently being
developed by Pfizer. The PI3K/Akt signaling pathway is a key pathway in
cell proliferation, growth, survival, protein synthesis, and glucose
metabolism. It has been recognized recently that inhibiting this pathway
might provide a viable therapy for cancer. PKI-587 has shown
excellent activity in vitro and in vivo, with antitumor efficacy in both
subcutaneous and orthotopic xenograft tumor models when administered
intravenously.
Current developer:
Pfizer Inc.
1: Dehnhardt CM, Venkatesan AM, Chen Z, Delos-Santos
E, Ayral-Kaloustian S, Brooijmans N, Yu K, Hollander I, Feldberg L,
Lucas J, Mallon R. Identification of 2-oxatriazines as highly potent
pan-PI3K/mTOR dual inhibitors. Bioorg Med Chem Lett. 2011 Aug
15;21(16):4773-8. Epub 2011 Jun 21. PubMed PMID: 21763134.
2: Mallon R, Feldberg LR, Lucas J, Chaudhary I, Dehnhardt C, Santos ED,
Chen Z, dos Santos O, Ayral-Kaloustian S, Venkatesan A, Hollander I.
Antitumor efficacy of PKI-587, a highly potent dual PI3K/mTOR kinase
inhibitor. Clin Cancer Res. 2011 May 15;17(10):3193-203. Epub 2011 Feb
15. PubMed PMID: 21325073.
3: Venkatesan AM, Chen Z, dos Santos O, Dehnhardt C, Santos ED,
Ayral-Kaloustian S, Mallon R, Hollander I, Feldberg L, Lucas J, Yu K,
Chaudhary I, Mansour TS. PKI-179: an orally efficacious dual
phosphatidylinositol-3-kinase (PI3K)/mammalian target of rapamycin (mTOR)
inhibitor. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5869-73. Epub 2010
Jul 30. PubMed PMID: 20797855.
4: Venkatesan AM, Dehnhardt CM, Delos Santos E, Chen Z, Dos Santos O,
Ayral-Kaloustian S, Khafizova G, Brooijmans N, Mallon R, Hollander I,
Feldberg L, Lucas J, Yu K, Gibbons J, Abraham RT, Chaudhary I, Mansour
TS. Bis(morpholino-1,3,5-triazine) derivatives: potent adenosine 5'-triphosphate
competitive phosphatidylinositol-3-kinase/mammalian target of rapamycin
inhibitors: discovery of compound 26 (PKI-587), a highly efficacious
dual inhibitor. J Med Chem. 2010 Mar 25;53(6):2636-45. PubMed PMID:
20166697.
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Email:
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(Keyword; CAS#; MedKoo code#)
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