Home Amines 1231929-97-7
1231929-97-7,MFCD22665744
Catalog No.:AA000K2I

1231929-97-7 | N-{5-[(4-ethylpiperazin-1-yl)methyl]pyridin-2-yl}-5-fluoro-4-(7-fluoro-3-isopropyl-2-methyl-1,3-benzodiazol-5-yl)pyrimidin-2-amine

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1mg
≥98%
in stock  
$53.00   $37.00
- +
25mg
99%(HPLC)
in stock  
$59.00   $42.00
- +
100mg
99%(HPLC)
in stock  
$126.00   $88.00
- +
250mg
97%
in stock  
$170.00   $119.00
- +
1g
97%
in stock  
$402.00   $282.00
- +
5g
97%
in stock  
$1,208.00   $846.00
- +
25g
97%
in stock  
$3,803.00   $2,662.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA000K2I
Chemical Name:
N-{5-[(4-ethylpiperazin-1-yl)methyl]pyridin-2-yl}-5-fluoro-4-(7-fluoro-3-isopropyl-2-methyl-1,3-benzodiazol-5-yl)pyrimidin-2-amine
CAS Number:
1231929-97-7
Molecular Formula:
C27H32F2N8
Molecular Weight:
506.5934
MDL Number:
MFCD22665744
SMILES:
CCN1CCN(CC1)Cc1ccc(nc1)Nc1ncc(c(n1)c1cc(F)c2c(c1)n(C(C)C)c(n2)C)F
Properties
Computed Properties
 
Complexity:
723  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
37  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
7  
XLogP3:
3.8  

Literature

Title: A Population Pharmacokinetic and Pharmacodynamic Analysis of Abemaciclib in a Phase I Clinical Trial in Cancer Patients.

Journal: Clinical pharmacokinetics 20180101

Title: Efficacy and Safety of Abemaciclib, an Inhibitor of CDK4 and CDK6, for Patients with Breast Cancer, Non-Small Cell Lung Cancer, and Other Solid Tumors.

Journal: Cancer discovery 20160701

Title: Optimising the combination dosing strategy of abemaciclib and vemurafenib in BRAF-mutated melanoma xenograft tumours.

Journal: British journal of cancer 20160315

Title: Overcoming Therapeutic Resistance in HER2-Positive Breast Cancers with CDK4/6 Inhibitors.

Journal: Cancer cell 20160314

Title: Targeting the cyclin D-cyclin-dependent kinase (CDK) 4/6-retinoblastoma pathway with selective CDK 4/6 inhibitors in hormone receptor-positive breast cancer: rationale, current status, and future directions.

Journal: Discovery medicine 20160101

Title: Brain Exposure of Two Selective Dual CDK4 and CDK6 Inhibitors and the Antitumor Activity of CDK4 and CDK6 Inhibition in Combination with Temozolomide in an Intracranial Glioblastoma Xenograft.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20150901

Title: A CDK4/6 inhibitor enhances cytotoxicity of paclitaxel in lung adenocarcinoma cells harboring mutant KRAS as well as wild-type KRAS.

Journal: Cancer biology & therapy 20130701

Title: The requirement for cyclin D function in tumor maintenance.

Journal: Cancer cell 20121016

Title: Therapeutic targeting of the cyclin D3:CDK4/6 complex in T cell leukemia.

Journal: Cancer cell 20121016

Title: Therapeutic response to CDK4/6 inhibition in breast cancer defined by ex vivo analyses of human tumors.

Journal: Cell cycle (Georgetown, Tex.) 20120715

Title: A synthetic lethal interaction between K-Ras oncogenes and Cdk4 unveils a therapeutic strategy for non-small cell lung carcinoma.

Journal: Cancer cell 20100713

Title: The landscape of somatic copy-number alteration across human cancers.

Journal: Nature 20100218

Title: Ku BM, et al. The CDK4/6 inhibitor LY2835219 has potent activity in combination with mTOR inhibitor in head and neck squamous cell carcinoma. Oncotarget.?2016 Mar 22;7(12):14803-13.

Title: Yadav V, et al. The CDK4/6 inhibitor LY2835219 overcomes PLX4032 resistance resulting from MAPK reactivation and cyclin D1 upregulation. Mol Cancer Ther. 2014 Oct;13(10):2253-63.

Title: Gelbert LM, et al. Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with NSC 613327. Invest New Drugs. 2014 Oct;32(5):825-37.

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Tags:1231929-97-7 Molecular Formula|1231929-97-7 MDL|1231929-97-7 SMILES|1231929-97-7 N-{5-[(4-ethylpiperazin-1-yl)methyl]pyridin-2-yl}-5-fluoro-4-(7-fluoro-3-isopropyl-2-methyl-1,3-benzodiazol-5-yl)pyrimidin-2-amine