SML1657
吉非替尼
≥98% (HPLC), powder, EGFR TK inhibitor
别名:
N-（3-氯-4-氟-苯基）-7-甲氧基-6-（3-吗啉-4-基丙氧基）喹唑啉-4-胺, ZD1839
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关于此项目
经验公式（希尔记法）:
C22H24ClFN4O3
化学文摘社编号:
分子量:
446.90
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
吉非替尼, ≥98% (HPLC)
SMILES string
COC(C=C(N=CN=C1NC2=CC(Cl)=C(F)C=C2)C1=C3)=C3OCCCN4CCOCC4
InChI key
XGALLCVXEZPNRQ-UHFFFAOYSA-N
InChI
1S/C22H24ClFN4O3/c1-29-20-13-19-16(12-21(20)31-8-2-5-28-6-9-30-10-7-28)22(26-14-25-19)27-15-3-4-18(24)17(23)11-15/h3-4,11-14H,2,5-10H2,1H3,(H,25,26,27)
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 10 mg/mL, clear
storage temp.
room temp
Quality Level
Gene Information
human ... EGFR(1956)
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Application
吉非替尼已用于：
- 研究其在子宫内膜癌治疗中的有效应用
- 细胞增殖、细胞周期和细胞凋亡试验
- 细胞活力测定和集落形成试验
Biochem/physiol Actions
吉非替尼是一种选择性表皮生长因子受体酪氨酸激酶 (EGFR TK) 抑制剂。吉非替尼具有抗肿瘤活性，已被批准用于治疗非小细胞肺癌 (NSCLC)。
吉非替尼对 EGFR 酪氨酸激酶结构域中 ATP（三磷酸腺苷）结合站点的亲和力高于 ATP。因此，已知吉非替尼可抑制子宫内膜癌的进展。
吉非替尼对 EGFR 酪氨酸激酶结构域中 ATP（三磷酸腺苷）结合站点的亲和力高于 ATP。因此，已知吉非替尼可抑制子宫内膜癌的进展。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Repr. 1B - Skin Irrit. 2 - STOT RE 2 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Baodan Yu et al.
Molecular medicine reports, 24(4) (2021-08-17)
Tyrosine kinase inhibitors, such as gefitinib, are currently widely used as targeted therapeutics for non‑small cell lung cancer (NSCLC). Although drug resistance has become a major obstacle to successful treatment, mechanisms underlying resistance to gefitinib remain unclear. Therefore, the present
Brian S Bogdanowicz et al.
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners, 23(3), 203-214 (2016-02-26)
Purpose The approval history, pharmacology, pharmacokinetics, clinical trials, efficacy, dosing recommendations, drug interactions, safety, place in therapy, and economic considerations of gefitinib are reviewed. Summary Lung cancer is one of the most commonly diagnosed cancers and is the leading cause
Hisanori Isomura et al.
Cancer science, 112(4), 1614-1623 (2021-01-29)
We previously reported that ROR1 is a crucial downstream gene for the TTF-1/NKX2-1 lineage-survival oncogene in lung adenocarcinoma, while others have found altered expression of ROR1 in multiple cancer types. Accumulated evidence therefore indicates ROR1 as an attractive molecular target
Silencing of long non-coding RNA MIAT sensitizes lung cancer cells to gefitinib by epigenetically regulating miR-34a.
Fu Y, et al.
Frontiers in Pharmacology, 9, 82-82 (2018)
P M Ellis et al.
Current oncology (Toronto, Ont.), 22(3), e183-e215 (2015-06-20)
This systematic review addresses the use of epidermal growth factor receptor (egfr) inhibitors in three populations of advanced non-small-cell lung cancer (nsclc) patients-unselected, selected, and molecularly selected-in three treatment settings: first line, second line, and maintenance. Ninety-six randomized controlled trials
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