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Cat. Number
10-2135
Chemical Name
10-2135 厄洛替尼·HCl Erlotinib · HCl 183319-69-9
CAS Number
183319-69-9
Mol. Formula
C22H23N3O4 HCl
Mol. Weight
429.91
Qty 1
10mg
Qty 2
100mg
Appearance
White or off-white solid
Application Notes
98% by TLC NMR (Conforms)
Synonym
N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine hydrochloride
Solubility
Soluble in DMSO (up to 18 mg/ml with warming).
Storage condition
-20℃
Stability
Stable for 1 year as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
References

Erlotinib HCl (182219-93-9) is a potent inhibitor of EGFR tyrosine kinase (IC50 = 2 nM).1 Potent inhibitor of mutant JAK2-V617F.2 Weaker inhibitor of ErbB-2 kinase (Ki = 1 μM) ErbB-4 kinase (Ki = 1.5 μM).3 HDAC inhibitors sensitize for erlotinib activity in EGFR-mutated and wildtype non-small cell lung cancer (NSCLC) cells.4 A clinically effective agent for NSCLC.5

References/Citations

1) Moyer et al. (1997), Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor tyrosine kinases; Cancer Res., 57 4838
2) Li et al. (2007), Erlotinib effectively inhibits JAK2V617F activity and polycythemia vera cell growth; J. Biol. Chem., 282 3428
3) Wood et al. (2004), A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells; Cancer Res., 64 6652
4) Greve et al. (2015), The pan-HDAC inhibitor panobinostat acts as a sensitizer for erlotinib activity in EGFR-mutated and –wildtype non-small cell lung cancer cells; BMC Cancer, 15 947
5) Minquet et al. (2016), Targeted therapies for treatment of non-small cell lung cancer-Recent advances and future perspectives; Int. J. Cancer, 138 2549

Focus Biomolecules supplier, chemical structure of Erlotinib HCl | EGFR Kinase inhibitor | CAS 183319-69-9

厄洛替尼·HCl   英文名称Erlotinib · HCl,货号10-2135 上海惠诚提供10mg 100mg 厄洛替尼·HCl Erlotinib · HCl,美国focus原装进口,咨询电话021-60498804

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