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AZD-9291

CAS No.
1421373-65-0
Chemical Name:
AZD-9291
Synonyms
Mereletinib;N-(2-{2-dimethylaminoethyl-methylamino}-4-methoxy-5-{[4-(1-methylindol-3-yl)pyrimidin-2-yl]amino}phenyl)prop-2-enamide;ZAD9291;Osimertinib Intermediate 4;N-(2-{[2-(Dimethylamino)ethyl](methyl)amino}-4-methoxy-5-{[4-(1-methyl-1H-indol-3-yl)pyrimidin;osim;CS-943;ADZ9291;Ochinib;AZD-9291
CBNumber:
CB02677059
Molecular Formula:
C28H33N7O2
Molecular Weight:
499.61
MDL Number:
MFCD27988062
MOL File:
1421373-65-0.mol
Last updated:2024-04-09 13:47:46

AZD-9291 Properties

Melting point >188oC (dec.)
Density 1.19±0.1 g/cm3(Predicted)
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly, Heated), Methanol (Slightly, Heated)
pka 12.68±0.70(Predicted)
form Solid
color Pale Yellow to Beige
CAS DataBase Reference 1421373-65-0
FDA UNII 3C06JJ0Z2O

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P362+P364-P332+P313-P337+P313-P403+P233-P405-P501
HS Code  29339900
NFPA 704
0
2 0

AZD-9291 price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 16237 AZD 9291 ≥98% 1421373-65-0 1mg $32 2024-03-01 Buy
Cayman Chemical 16237 AZD 9291 ≥98% 1421373-65-0 5mg $86 2024-03-01 Buy
Cayman Chemical 16237 AZD 9291 ≥98% 1421373-65-0 10mg $139 2024-03-01 Buy
Cayman Chemical 16237 AZD 9291 ≥98% 1421373-65-0 50mg $381 2024-03-01 Buy
TRC A808075 AZD9291(Osimertinib) 1421373-65-0 10mg $105 2021-12-16 Buy
Product number Packaging Price Buy
16237 1mg $32 Buy
16237 5mg $86 Buy
16237 10mg $139 Buy
16237 50mg $381 Buy
A808075 10mg $105 Buy

AZD-9291 Chemical Properties,Uses,Production

Uses

AZD-9291 (Osimertinib) is a oral, third generation, small-molecule epidermal growth factor receptor (EGFR) inhibitor and antineoplastic agent. In addition, it is a Cytochrome P450 3A inhibitor, and Cytochrome P450 3A4 Inducer, and Cytochrome P450 1A2 Inducer, and Breast Cancer Resistance Protein Inhibitor. It is used for the treatment of advanced non-small cell lung cancer (NSCLC) where mutant EGFR form (such as T790M) is often presented. Through suppressing the EGFR-mediated signalling, it cause cell death and inhibit tumour growth in related cancer cells. 

Description

AZD-9291 (Mesylate), also known as Osimertinib, belongs to a third-generation EGFR (epidermal growth factor receptor) inhibitor. It can be used for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) in case when the cancer cells carry specific mutations (such as T790M) in the epidermal growth factor receptor. It takes effect through directly binding to the certain mutant forms of EGFR (T790M, L858R, and exon 19 deletions) that are frequently found in NSCLC, further causing poor prognosis for late-stage disease. Since it spares wild type EGFR during therapy, it has only limited toxicity.

Uses

AZD 9291 is an irreversible inhibitor of epidermal growth factor receptor (EGFR) sensitizing and T790M resistance mutations (IC50s = 15-17 nM) while sparing the wild-type form of the receptor (IC50 = 480 nM). It binds the related IGF1R and hERG receptors with significantly reduced potency (IC50s = 2.9 and 16.2 μM, respectively). AZD 9291 has been shown to inhibit tumor growth in a xenograft mouse model at oral doses of 5-10 mg/kg and has been tested clinically in patients with advanced EGFR mutant non-small-cell lung cancer.[Cayman Chemical]

Indications

The collection of ibrutinib (Imbruvica(R), Pharmacyclics Inc.), afatinib, and osimertinib represents the small, yet expanding, group of covalent SMKIs. Ibrutinib is a non-receptor Bruton’s tyrosine kinase inhibitor approved for the treatment of relapsed chronic lymphocytic leukemia. Afatinib, approved for NSCLC in 2013 and squamous NSCLC in 2016, is a second-generation irreversible EGFR inhibitor that targets wild-type EGFR, the mutant T790M EGFR, and HER2. Osimertinib (AZD9291), which was approved by FDA in November 2015, is a third-generation irreversible EGFR inhibitor that selectively targets the mutant T790M EGFR. Rociletinib, which shares a high degree of structural similarity with that of osimertinib, is a promising covalent EGFR inhibitor developed by Clovis Oncology aimed for the treatment of patients with EGFR T790M-mutated NSCLC, until the company terminated its development in May 2016 following a negative vote fromthe FDA’sOncologic Drugs Advisory Committee.

Definition

ChEBI: A member of the class of aminopyrimidines that is 4-(1-methylindol-3-yl)pyrimidin-2-amine in which one of the amino hydrogens is replaced by a 2-methoxy-4-[2-(dimethylamino)ethyl](methyl)amino-5-acrylamidophenyl group. Used (as the mesylate salt) for treat ent of EGFR T790M mutation positive non-small cell lung cancer.

target

Exon 19 deletion EGFR

References

http://www.medkoo.com/products/6711
https://en.wikipedia.org/wiki/Osimertinib
https://www.drugbank.ca/drugs/DB09330

1421372-66-8
79-10-7
1421373-65-0
Synthesis of AZD-9291 from Mutated EGFR-IN-1 and Acrylic acid
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View Lastest Price from AZD-9291 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	AZD-9291 pictures 2024-04-09 AZD-9291
1421373-65-0
US $5.00-0.10 / KG 1KG 98% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Osimertinib (AZD9291) pictures 2024-03-12 Osimertinib (AZD9291)
1421373-65-0
US $0.00 / g 1g 98% HPLC 1KG shandong perfect biotechnology co.ltd
AZD-9291 pictures 2023-11-27 AZD-9291
1421373-65-0
US $0.00 / g 10g 99% 50kg Wuhan Senwayer Century Chemical Co.,Ltd
  • 	AZD-9291 pictures
  • AZD-9291
    1421373-65-0
  • US $5.00-0.10 / KG
  • 98%
  • Henan Fengda Chemical Co., Ltd
  • AZD-9291 pictures
  • AZD-9291
    1421373-65-0
  • US $0.00 / g
  • 99%
  • Wuhan Senwayer Century Chemical Co.,Ltd

AZD-9291 Spectrum

N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide Mereletinib mesylate(AZD9291) AZD9291 (free base) Osimertinib (AZD-9291) AZD9291, Osimertinib AZD9291 Base Osimertinib Base AZD9291 10G AZD-9291 N(2{[2(diMethylaMino)ethyl](Methyl)aMino}4Methoxy5{[4(1Methyl1Hindol3yl)pyriMidin2yl]aMino}phenyl)prop2enaMide N-[2-[[2-(Dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-2-propenamide AZD9291,AZD-9291 2-Propenamide, N-[2-[[2-(dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]- AZD9291 N-[2-[[2-(Dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-2-propenamide N-[2-[[2-(Dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-2-propenamide AZD9291 AZD9291, >=98% AZD929/Osimertinib Osimertinib, 98%, a potent and selective mutated forms EGFR inhibitor Pharmaceutical Chemical Anticancer Drug Azd-9291 for for Lung Cancer 1421373-65-0 N1-[2-(Dimethylamino)ethyl]-2-methoxy-N1-methyl-N4-[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]-1,4-benzenetriamine AZD-92941 CS-943 ADZ9291 Mereletinib(AZD-9291,Osimertinib) EGFR INHIBITOR; AZD9291; AZD 9291;TAGRISSO osim EGFR INHIBITOR;AZD9291;AZD 9291;TAGRISSO;OSIMERTINIB;MERELETINIB Ochinib N-(2-{2-dimethylaminoethyl-methylamino}-4-methoxy-5-{4-(1-methylindol-3-yl)pyrimidin-2-yl}amino}phenyl)prop-2enamide (AZD9291 free base) )amino)-4-methoxy-5-((4-(1-methyL N-(2-((2-(DimethyL AZD-9291 USP/EP/BP N-(2-{2-dimethylaminoethyl-methylamino}-4-methoxy-5-{[4-(1-methylindol-3-yl)pyrimidin-2-yl]amino}phenyl)prop-2-enamide Mereletinib ZAD9291 N-(2-{[2-(Dimethylamino)ethyl](methyl)amino}-4-methoxy-5-{[4-(1-methyl-1H-indol-3-yl)pyrimidin Osimertinib Intermediate 4 Ethanone,1-[5-bromo-3-(trifluoromethyl)-6-pyridinyl]- 13C,2H3]-Osimertinib Osimeitinib 1421373-65-0 421373-65-0 1421273-65-0 C28H33N7O2 Inhibitors API Anticancer AZD9291 1421373-65-0