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Neratinib

CAS No.
698387-09-6
Chemical Name:
Neratinib
Synonyms
(2e)-n-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide;CS-26;PB-272;101028;neratinib;nevatinib;PF-0528767;WAY-179272;Unii-jjh94R3pwb;Neratinib Base.
CBNumber:
CB2855051
Molecular Formula:
C30H29ClN6O3
Molecular Weight:
557.04
MDL Number:
MFCD09752958
MOL File:
698387-09-6.mol
Last updated:2023-12-22 17:53:22

Neratinib Properties

Melting point 185-187°C
Boiling point 757.0±60.0 °C(Predicted)
Density 1.33
storage temp. Refrigerator
solubility Chloroform (Slightly), DMSO (Slightly, Heated, Sonicated), Methanol (Slightly, Heated)
form Off-white solid.
pka 12.37±0.43(Predicted)
color Pale Yellow to Yellow
FDA UNII JJH94R3PWB
ATC code L01EH02

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314-H290
Precautionary statements  P501-P234-P264-P280-P390-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P406-P405
HS Code  29334900

Neratinib price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18404 Neratinib ≥98% 698387-09-6 50 mg $97 2024-03-01 Buy
Cayman Chemical 18404 Neratinib ≥98% 698387-09-6 100 mg $150 2024-03-01 Buy
Cayman Chemical 18404 Neratinib ≥98% 698387-09-6 5mg $43 2023-01-06 Buy
Cayman Chemical 18404 Neratinib ≥98% 698387-09-6 1mg $35 2021-12-16 Buy
Cayman Chemical 18404 Neratinib ≥98% 698387-09-6 10mg $43 2024-03-01 Buy
Product number Packaging Price Buy
18404 50 mg $97 Buy
18404 100 mg $150 Buy
18404 5mg $43 Buy
18404 1mg $35 Buy
18404 10mg $43 Buy

Neratinib Chemical Properties,Uses,Production

New anticancer drug

Neratinib developed by US Wyeth company is an irreversible epidermal growth factor receptor(EGFR) inhibitor. It is a multiple target point of small molecule tyrosine kinase inhibitors to HER 2 and HER1 after Lapatinib, and is an irreversible ErbB receptor tyrosine kinase inhibitor. Neratinib could selectively inhibit HER-1 and HER-2 of EGFR family(IC50 was 92 nmol/L and 59 nmol/L, respectively). Clinical research showed that Neratinib exerted significant therapeutic effect on non-small cell lung cancer, colon cancer, and breast cancer.
The phaseⅡclinical trial indicated that Neratinib showed good efficacy and tolerance to HER-2 positive patients with advanced breast cancer who had been received or not Trastuzumab treatment.
The phase Ⅲ breast cancer clinical trial was complete in September 2014. The data indicated that the efficacy of Neratinib was better than Roche's Herceptin in treatment of HER-2 positive early breast cancer.
The above information is edited by the Chemicalbook of Liu Yujie.

Genotoxicity

Neratinib and its metabolites were not genotoxic. Administration of neratinib to pregnant rabbits during organogenesis resulted in abortions, embryo-fetal death, and fetal abnormalities at maternal exposures (AUC) approximately 0.2 times exposures in patients at the recommended dose. Oral administration of neratinib to pregnant rats from gestation day 7 until lactation day 20 resulted in effects on long-term memory in male offspring at maternal doses less than the maximum recommended clinical dose on a mg/m2 basis. Neratinib was not carcinogenic in a 26-week carcinogenicity study in rasH2 transgenic mice.

Clinical trial

Neratinib was tested in a phase II trial as monotherapy in 2 cohorts of patients with advanced HER2-positive breast cancer those with and those without previous trastuzumab treatment. Sixteen-week progression-free survival (PFS) rates were 59% for patients with previous trastuzumab treatment and 78% for patients with no previous trastuzumab treatment with a median PFS of 22.3 and 39.6 weeks, respectively. Objective response rates were 24% among patients with previous trastuzumab treatment and 56% in the trastuzumab-naive cohort.[4]

Synthesis pathways

3-chloro-4-(pyridin-2-yl-methoxy)-aniline (2) and N-(4-chloro-3-cyano-7-ethoxy-quinolin-6-yl)-acetamide (3) are used as raw material to prepare N-[4-[3-chloro-4-(pyridin-2-yl-methoxy) anilino]-3-cyano-7-ethoxy-quinolin-6-yl] acetamide (4) by nucleophilic substitution. Deprotection of 4 was under the effect of hydrochloric acid, then was precipitated the free base in methanol solution of potassium carbonate to prepare 6-amino-3-cyano-4-[3-chloro-4-(pyridin-2-yl-methoxy) anilino]-7-ethoxy-quinoline (5). Neratinib(1) was obtained by condensation of 5 and acyl chloride which was prepared by trans-4-dimethylamino-crotonic acid hydrochloride (6).
Synthesis pathways of Neratinib
Figure 1 Synthesis pathways of Neratinib

Side Effects

Diarrhea, nausea, vomiting, and fatigue.

Description

The receptor tyrosine kinase HER2 (ErbB2) is a key component of epidermal growth factor receptor complexes that are known to have central roles in cell proliferation and cancer. Neratinib is an orally active, irreversible inhibitor of the HER2 kinase (IC50 = 59 nM). It also potently inhibits several mutants of HER2 and shows 10-fold or greater selectivity over a wide variety of other kinases. As an irreversible inhibitor, neratinib may circumvent acquired resistance developed against reversible inhibitors, including gefitinib . Neratinib has been evaluated in clinical trials against cancers characterized by HER2 overexpression or HER2 activating mutations.

Uses

An oral, irreversible dual EGFR/HER2 inhibitor for breast and non-small cell lung cancer. Antitumor agent.

Uses

Neratinib (HKI-272) is a highly selective HER2 and EGFR inhibitor with IC50 of 59 nM and 92 nM, respectively.

Definition

ChEBI: A quinoline compound having a cyano group at the 3-position, a 3-chloro-4-(2-pyridylmethoxy)anilino group at the 4-position, a 4-dimethylamino-trans-but-2-enamido group at the 6-position, and an ethoxy group at the 7-position.

target

HER2

storage

Store at -20°C

52334-92-6
1269662-79-4
698387-09-6
Synthesis of Neratinib from 2-(DIMETHYLAMINO)ACETALDEHYDE and Phosphonic acid, P-[2-[[4-[[3-chloro-4-(2-pyridinylmethoxy)phenyl]amino]-3-cyano-7-ethoxy-6-quinolinyl]amino]-2-oxoethyl]-, diethyl ester
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View Lastest Price from Neratinib manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Neratinib (HKI-272) pictures 2024-03-12 Neratinib (HKI-272)
698387-09-6
US $0.00 / g 1g 98% HPLC 1KG shandong perfect biotechnology co.ltd
Neratinib pictures 2023-12-23 Neratinib
698387-09-6
US $0.00-0.00 / kg 1kg 99%,single impurity<0.1 1 ton Nanjing Fred Technology Co., Ltd
Neratinib pictures 2023-11-27 Neratinib
698387-09-6
US $0.00 / KG 1KG 99% 20 TONS Wuhan Senwayer Century Chemical Co.,Ltd
  • Neratinib pictures
  • Neratinib
    698387-09-6
  • US $0.00-0.00 / kg
  • 99%,single impurity<0.1
  • Nanjing Fred Technology Co., Ltd
  • Neratinib pictures
  • Neratinib
    698387-09-6
  • US $0.00 / KG
  • 99%
  • Wuhan Senwayer Century Chemical Co.,Ltd
Neratinib(HKI-272) (2E)-N-[4-[[3-chloro-4-(2-pyridinylMethoxy)phenyl]aMino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(diMethylaMino)-2-butenaMide neratinib (E)-N-[4-[3-Chloro-4-[(2-pyridinyl)methoxy]anilino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide N-(4-(3-Chloro-4-(2-pyridinylmethoxy)anilino)-3-cyano-7-ethoxy-6-quinolyl)-4-(dimethylamino)-2-butenamide Unii-jjh94R3pwb (2e)-n-(4-((3-chloro-4-((pyridin-2-yl)Methoxy)phenyl)aMino)-3-cyano-7-ethoxyquinolin-6-yl)-4-(diMethylaMino)but-2-enaMide neratinib HKI-272 Neratinib Neratinib HKI-272 (2E)-N-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide Neratinib (2E)-N-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide (2E)-N-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-emide PB272(neratinib) 2-ButenaMide,N-[4-[[3-chloro-4-(2-pyridinylMethoxy)phenyl]aMino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(diMethylaMino)-,(2E)- Neratinib, >=99% PB-272 PF-0528767 WAY-179272 (E)-N-(4-(3-Chloro-4-(pyridin-2-yLmethoxy)phenylamino)-3-cyano-7-ethoxyquinolin-6-yl)-4-(dimet Neratinib USP/EP/BP Lenatinib Impurity E 101028 nevatinib Neratinib, 99%, a highly selective HER2 and EGFR inhibitor Neratinib API and intermediates CS-26 HKI-272; HKI272; HKI 272 (2e)-n-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide (2E)-N-[4-[[3-chloro-4-[(pyridin-2-yl)methoxy]phenyl]amino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide Neratinib Base. 698387-09-6 688387-09-6 C30H29ClN6O3 C30H31ClN6O2 Inhibitors Anti-cancer & immunity Antineoplastic API