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- Afatinib (BIBW2992)
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- Afatinib (BIBW2992)
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- JAK/STAT Signaling
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- Afatinib (BIBW2992)
Afatinib (BIBW2992)
Afatinib (BIBW2992), an irreversible inhibitor of the ErbB family of tyrosine kinases, downregulates ErbB signalling by binding to the kinase domains of epidermal growth factor receptor (EGFR)/ human epidermal growth factor receptor 2 (HER2) with IC50 of 0.5 nM and 14nM, respectively.
The ErbB receptor tyrosine kinase family consists of four cell surface receptors: ErbB1/ EGFR/HER1, ErbB2/HER2, ErbB3/HER3, and ErbB4/HER4. It has been shown that EGFR and HER2 play important roles in the development and progression of certain aggressive types of cancers and inflammation-associated diseases.
Afatinib was shown to suppress EGF-induced phosphorylation of EGFR and cell proliferation in a variety of EGFR-overexpressing and HER2-expressing cell lines such as A431, NIH-3T3-HER2, NCI-N87 and BT-474 [1].
The component has also been used extensively in various animal models to study the role of EGFR/HER2. Oral administration of afatinib inhibited cancer cell growth and survival and suppress the tumor regression in xenograft and transgenic lung cancer models [2]. In addition, afatinib is identified as EGFR blocker which was approved for the treatment of patients with EGFR-mutated nonsmall cell lung cancer [3].
References:
1.Eskens FA, Mom CH, Planting AS, Gietema JA, Amelsberg A, Huisman H, et al. A phase I dose escalation study of BIBW 2992, an irreversible dual inhibitor of epidermal growth factor receptor 1 (EGFR) and 2 (HER2) tyrosine kinase in a 2-week on, 2-week off schedule in patients with advanced solid tumours. Br J Cancer 2008,98:80-85.
2.Li D, Ambrogio L, Shimamura T, Kubo S, Takahashi M, Chirieac LR, et al. BIBW2992, an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models. Oncogene 2008,27:4702-4711.
3.Engle JA, Kolesar JM. Afatinib: A first-line treatment for selected patients with metastatic non-small-cell lung cancer. Am J Health Syst Pharm 2014,71:1933-1938.
- 1. White SM, Avantaggiati ML, et al. "YAP/TAZ Inhibition Induces Metabolic and Signaling Rewiring Resulting in Targetable Vulnerabilities in NF2-Deficient Tumor Cells." Dev Cell. 2019 May 6;49(3):425-443.e9. PMID:31063758
- 2. Huang L, Cai M, et al."Combinational therapy of crizotinib and afatinib for malignant pleural mesothelioma. Am J Cancer Res." 2017 Feb 1;7(2):203-217. eCollection 2017. PMID:28337371
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 485.94 |
Cas No. | 439081-18-2 |
Formula | C24H25ClFN5O3 |
Solubility | ≥24.3 mg/mL in DMSO; insoluble in H2O; ≥42.1 mg/mL in EtOH with ultrasonic |
Chemical Name | (E)-N-[4-(3-chloro-4-fluoroanilino)-7-[(3S)-oxolan-3-yl]oxyquinazolin-6-yl]-4-(dimethylamino)but-2-enamide |
SDF | Download SDF |
Canonical SMILES | CN(C)CC=CC(=O)NC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC(=C(C=C3)F)Cl)OC4CCOC4 |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Cell experiment: [1] | |
Cell lines |
NCI-H1975 and BT474 cells |
Preparation method |
The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while.Stock solution can be stored below -20°C for several months. |
Reaction Conditions |
EC50: 92 nM for NCI-H1975 cells, 54 nM for BT474 cells; 96 hours |
Applications |
The effect of the inhibitor on cellular proliferation was tested in various assay formats including anchorage-dependent (BT474 cells grown on plastic; two-dimensional assays) and anchorage-independent (NCI-H1975 cells grown in soft agar; three-dimensional assays) assays. Afatinib dose-dependently inhibited cell proliferation and showed nanomolar activity. The EC50 values for NCI-H1975 and BT474 cells were 92 nM and 54 nM, respectively. |
Animal experiment: [2] | |
Animal models |
Transgenic mice expressing the delE748-A752 version of mouse Egfr and the L858R version of human EGFR |
Dosage form |
Oral administration, 5 mg/kg, once daily, 5 days per week |
Applications |
The transgenic mice received the oral administration of the drug until toxicity or death. All mice in the control group died, with a median survival time of 119 days. Afatinib treatment significantly enhanced the survival of transgenic mice with a median survival time of 456 days. No toxic death was observed in any mice. Four weeks after the initiation of treatment, body weight in the control group was significantly lower than in the afatinib group. |
Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
References: [1] Solca F, Dahl G, Zoephel A, et al. Target binding properties and cellular activity of afatinib (BIBW 2992), an irreversible ErbB family blocker. Journal of Pharmacology and Experimental Therapeutics, 2012, 343(2): 342-350. [2] Ninomiya T, Takigawa N, Ichihara E, et al. Afatinib prolongs survival compared with gefitinib in an epidermal growth factor receptor-driven lung cancer model. Molecular cancer therapeutics, 2013, 12(5): 589-597. |
Description | Afatinib (BIBW2992) is an irreversible inhibitor of EGFR/HER2 for EGFR(wt), EGFR(L858R), EGFR(L858R/T790M) and HER2 with IC50 of 0.5 nM, 0.4 nM, 10 nM and 14 nM, respectively; 100-fold more active against Gefitinib-resistant L858R-T790M EGFR mutant. | |||||
Targets | EGFRwt | EGFRL858R | EGFR L858R/T790M | HER2 | ||
IC50 | 0.5 nM | 0.4 nM | 10 nM | 14 nM |
Quality Control & MSDS
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