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Alflutinib

CAS No.
1869057-83-9
Chemical Name:
Alflutinib
Synonyms
Firmonertinib;ASK120067;Aflutinib;Alflutinib;Capsaicin Impurity 17;Firmonertinib Alflutinib;Alflutinib, 10 mM in DMSO;Alflutinib (Firmonertinib);AST2818;AST-2818;ASK120067;Alflutinib,inhibit,esistant mutation,T790M,EGFR,AST 2818,Furmonertinib,Inhibitor,ErbB-1,NSCLC,cancer,Epidermal growth factor receptor,AST-2818,HER1
CBNumber:
CB84844457
Molecular Formula:
C28H31F3N8O2
Molecular Weight:
568.61
MDL Number:
MOL File:
1869057-83-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41
Product description Number Pack Size Price
Aflutinib UZC05783 500mg $15125
Aflutinib UZC05783 1000mg $19250
Firmonertinib 99.89% CS-0067172 5mg $173
Firmonertinib 99.89% CS-0067172 10mg $260
Firmonertinib 99.89% CS-0067172 25mg $520

Alflutinib Properties

Density 1.29±0.1 g/cm3(Predicted)
form Solid
pka 11+-.0.70(Predicted)
color White to off-white
InChIKey GHKOONMJXNWOIW-UHFFFAOYSA-N
SMILES CN1C2=CC=CC=C2C(C2C=CN=C(NC3C=C(NC(=O)C=C)C(N(C)CCN(C)C)=NC=3OCC(F)(F)F)N=2)=C1
FDA UNII A49A7A5YN4

Alflutinib price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth UZC05783 Aflutinib 1869057-83-9 500mg $15125 2026-06-05 Buy
Biosynth UZC05783 Aflutinib 1869057-83-9 1000mg $19250 2026-06-05 Buy
ChemScene CS-0067172 Firmonertinib 99.89% 1869057-83-9 5mg $173 2026-06-04 Buy
ChemScene CS-0067172 Firmonertinib 99.89% 1869057-83-9 10mg $260 2026-06-04 Buy
ChemScene CS-0067172 Firmonertinib 99.89% 1869057-83-9 25mg $520 2026-06-04 Buy
Product number Packaging Price Buy
UZC05783 500mg $15125 Buy
UZC05783 1000mg $19250 Buy
CS-0067172 5mg $173 Buy
CS-0067172 10mg $260 Buy
CS-0067172 25mg $520 Buy

Alflutinib Chemical Properties,Uses,Production

Uses

Firmonertinib (Alflutinib; Furmonertinib) is an orally active, mutant-selective, and highly brain penetrant EGFR inhibitor. Firmonertinib inhibits EGFR active mutations as well as the T790M acquired resistant mutation. Firmonertinib has the potential for the research of cancer diseases, especially advanced non-small cell lung cancer (NSCLC) with EGFR ex20ins mutation[1].

Mechanism of action

As a third-generation EGFR TKI, Alflutinib can irreversibly bind to the EGFR protein, especially to tumor cells carrying the T790M drug-resistant mutation. This specific binding helps reduce damage to normal cells while effectively inhibiting the proliferation of tumor cells.

Synthesis

Arylation of the indole prepared the chloropyridine 21.7, which was then reacted with the aniline 21.4 in the presence of excess p-toluenesulfonic acid to produce 21.8 (see Figure 7.3.2). The second SNAr reaction used the diamine 21.9, which was coprecipitated with water in DMF to give the amine 21.10 in 77% yield over a two-step reaction. Reduction of the nitro group using sodium sulfite gave the corresponding amine under metal-free and mild conditions. The crude aniline was then converted to the dihydrochloride salt 21.11, which was isolated as a solid in high purity (99.8%) and yield (94%) after slurrying in methanol and ethanol. Finally, a two-step approach was used to install the α,β-unsaturated amide, as opposed to the earlier route that used acryloyl chloride directly. The acylation reaction used the chloroacyl chloride 21.12 to give the alkyl chloride 21.13, which was isolated by filtration. Subsequently, an elimination reaction was carried out with triethylamine at reflux in acetonitrile to prepare alflutinib (21) in 93% yield and 99.2% purity.
Alflutinib

IC 50

EGFR

References

[1] Y. Shi, et al. P2.03-028 Third Generation EGFR Inhibitor AST2818 (Alflutinib) in NSCLC Patients with EGFR T790M Mutation: A phase1/2 Multi-Center Clinical Trial.
[2] Alexander I. Spira, et al. FURVENT: Phase 3 trial of furmonertinib vs chemotherapy as first-line treatment for advanced NSCLC with EGFR exon 20 insertion mutations (FURMO-004). Journal of Clinical Oncology. Volume 42, Number 16_suppl.

Alflutinib Preparation Products And Raw materials

Raw materials

Preparation Products

Alflutinib Suppliers

Global( 40)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 sales@sarms4muscle.com China 10378 58
Zhengzhou Anbu Chem Co.,Ltd
+86-0371-88006763; +86-15988602810 sales@anbuchem.com China 5812 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +86-15965530500 nickzhang@hangyubiotech.com China 9930 58
CAREBIO PHARMA 18501057619 18501057619 yongfan@carebiopharm.com China 275 58
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4773 55
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4861 55
Shanghai Send Pharmaceutical Technology Co., Ltd. 021-58088081 18317173152 Hailey@shsendpharm.com China 846 55
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60

View Lastest Price from Alflutinib manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Alflutinib pictures 2026-07-27 Alflutinib
1869057-83-9
$55.00-197.00 99.87% 10g TargetMol Chemicals Inc.
  • Alflutinib pictures
  • Alflutinib
    1869057-83-9
  • $55.00-197.00
  • 99.87%
  • TargetMol Chemicals Inc.

Alflutinib Spectrum

Alflutinib AST2818;AST-2818;ASK120067 2-Propenamide, N-[2-[[2-(dimethylamino)ethyl]methylamino]-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]-6-(2,2,2-trifluoroethoxy)-3-pyridinyl]- Alflutinib,inhibit,esistant mutation,T790M,EGFR,AST 2818,Furmonertinib,Inhibitor,ErbB-1,NSCLC,cancer,Epidermal growth factor receptor,AST-2818,HER1 Firmonertinib Alflutinib N-(2-{[2-(dimethylamino)ethyl](methyl)amino}-5-{[4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl]amino}-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)prop-2-enamide Capsaicin Impurity 17 Alflutinib, 10 mM in DMSO Alflutinib (Firmonertinib) Aflutinib ASK120067 Firmonertinib 1869057-83-9 C28H31F3N8O2