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Detail of "698387-09-6"

  • CAS Number:
  • 698387-09-6
  • Name:
  • 2-Butenamide,N-[4-[[3-chloro-4-(2-pyridinylmethoxy)phenyl]amino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-,(2E)-

  • Superlist Name:
  • Neratinib
  • Molecular Structure:
  • Formula:
  • C30H29ClN6O3
  • Molecular Weight:
  • 557.04
  • Synonyms:
  • (E)-N-[4-[3-Chloro-4-[(2-pyridinyl)methoxy]anilino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide;(E)-N-[4-[[3-Chloro-4-((pyridin-2-yl)methoxy)phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)-2-butenamide;HKI 272;HKI-272(Neratinib);
  • Density:
  • 1.337 g/cm3
  • Boiling Point:
  • 756.97 °C at 760 mmHg
  • Flash Point:
  • 411.601 °C

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CAS No.698387-09-6 NeratinibCompetitive Product

Assay:99%  Appearance:white  Package:10 20 30

Min. Order:10Gram

Supplier:Shanghai Taibao Pharmaceutical Technology Co., Ltd [ China (Mainland)]

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CAS No.698387-09-6 NeratinibCompetitive Product

Assay:99%  Appearance:White or alm...

Molecular Weight:557.04 Density:1.337 g cm3 Boiling Point:756.97 C at 760 mmHg Flash Point:411.601 C...

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CAS No.698387-09-6 Neratinib

Assay:≥99%(HPLC)  Appearance:Inqury  Package:1G,5G,69G

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CAS No.698387-09-6 Neratinib

HKI-272, Neratinib

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24 hours Email contact is available, your email will be answered at the first time

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CAS No.698387-09-6 Neratinib

Neratinib CAS:698387-09-6 (2E)-N-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide

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Neratinib

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Neratinib

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Neratinib

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Assay:>98%

HKI-272(Neratinib)/HKI272 Brand Name :Biochempartner M.Wt: 557.04 Formula: C30H29ClN6O3 Solubility: Soluble in DMSO at 20 mg/mL Storage: Storage at -20C 2 years

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CAS No.698387-09-6 Neratinib

Neratinib is an orally available, irreversible tyrosine kinase inhibitor with IC50 of 59 nM and 92 nM for HER2 and EGFR, respectively.

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Reference

Epidermal Growth Factor Receptor Inhibitors in Development for the Treatment of Non-Small Cell Lung Cancer
All Rights Reserved. Epidermal Growth Factor Receptor Inhibitors in Development for the Treatment of Non-Small Cell Lung Cancer. Heymach, John V.; Nilsson, Monique; Blumenschein, George; Papadimitrakopoulou, Vassiliki; Herbst, Roy (Department of Thoracic/Head, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030-4009, USA). Clinical Cancer Research, 12(14, Pt. 2), 4441s-4445s (English) 2006 American Association for Cancer Research. CODEN: CCREF4. ISSN: 1078-0432. DOCUMENT TYPE: Journal; General Review CA Section: 1 (Pharmacology) Section cross-reference(s): 15 A review. The epidermal growth factor receptor (EGFR) inhibitors erlotinib, gefitinib, and cetuximab have undergone extensive clin. testing and have established clin. activity in non-small cell lung cancer and other types of solid tumors. A no. of newer inhibitors are currently in clin. development with different spectra of activity or mechanisms of receptor inhibition. These include monoclonal antibodies, such as panitumumab and matuzumab; dual inhibitors of EGFR and vascular endothelial growth factor receptor, such as ZD6474 and AEE788; inhibitors of multiple EGFR family members, such as lapatinib; and irreversible inhibitors, such as canertinib and HKI272. Preclin. studies suggest that several of these agents may have activity in tumors refractory to erlotinib or gefitinib. Among these agents, ZD6474 has undergone the most extensive clin. testing. The antitumor activity of ZD6474 in these two randomized phase II clin. trials in patients with non-small cell lung cancer was felt to be sufficiently promising to warrant phase III clin. testing. Several of the other EGFR inhibitors are also undergoing advanced clin. testing, either alone or in combination with other agents. EGFR has now been validated as a clin. relevant target, and several different types of agents inhibiting this receptor are currently in development. Future research will be needed to elucidate the role of these agents in patients with EGFR inhibitor-naive and EGFR inhibitor-refractory disease, to define the mol. characteristics that predict response, and to det. whether these drugs should be used in combination with other targeted agents or chemotherapy.Except for chemicals metioned above, 497839-62-0 and 698387-09-6 are also used. .
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