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Lapatinib

CAS No.
231277-92-2
Chemical Name:
Lapatinib
Synonyms
Tykerb;Tyverb;CS-220;GW-2016;CS-1860;GW 57201;Rapatini;lapatinib;GSK572016;GW-572016
CBNumber:
CB8855402
Molecular Formula:
C29H26ClFN4O4S
Molecular Weight:
581.06
MDL Number:
MFCD09264194
MOL File:
231277-92-2.mol
Last updated:2024-03-16 07:03:48

Lapatinib Properties

Melting point 144-146oC
Boiling point 750.7±60.0 °C(Predicted)
Density 1.381±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility Soluble in DMSO (up to 200 mg/ml)
form solid
pka 6.34±0.19(Predicted)
color Yellow
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.
InChIKey BCFGMOOMADDAQU-UHFFFAOYSA-N
SMILES N1=C2C(C=C(C3=CC=C(CNCCS(C)(=O)=O)O3)C=C2)=C(NC2=CC=C(OCC3=CC=CC(F)=C3)C(Cl)=C2)N=C1
CAS DataBase Reference 231277-92-2(CAS DataBase Reference)
FDA UNII 0VUA21238F
NCI Dictionary of Cancer Terms GW572016; Tykerb
NCI Drug Dictionary Tykerb
ATC code L01EH01

Pharmacokinetic data

Protein binding >99%
Excreted unchanged in urine <2%
Biological half-life 24 / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H362-H413
Precautionary statements  P201-P260-P263-P273-P305+P351+P338-P308+P313
HS Code  29349990
NFPA 704
0
2 0

Lapatinib price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 11493 Lapatinib ≥98% 231277-92-2 5mg $57 2024-03-01 Buy
Cayman Chemical 11493 Lapatinib ≥98% 231277-92-2 10mg $73 2024-03-01 Buy
Cayman Chemical 11493 Lapatinib ≥98% 231277-92-2 25mg $111 2024-03-01 Buy
Cayman Chemical 11493 Lapatinib ≥98% 231277-92-2 100mg $241 2024-03-01 Buy
Tocris 6811 Lapatinib ≥98%(HPLC) 231277-92-2 10 $48 2021-12-16 Buy
Product number Packaging Price Buy
11493 5mg $57 Buy
11493 10mg $73 Buy
11493 25mg $111 Buy
11493 100mg $241 Buy
6811 10 $48 Buy

Lapatinib Chemical Properties,Uses,Production

Indications and Usage

Lapatinib is a drug targeting breast cancer developed by British GlaxoSmithKline Co.
Human ErbB receptors belong to the type I tyrosine kinase (TK) receptor family, including ErbB1 (EGFR), ErbB2 (HER2), ErbB3 (HER3), and ErbB4 (HER4). The ErbB-1 (EGFR) and ErbB-2 (HER-2) receptors are often overexpressed or otherwise altered in cancer patients. Human epidermal growth factor receptor 2 (ErbB-2, HER-2) is known to be a human oncogene closely related with breast cancer. Its high expression in breast cancer often predicts lymph node metastasis and poor tumor differentiation, with poor prognosis. HER-2 is one of the target molecules for breast cancer-specific therapy. Lapatinib can act simultaneously on both Her-1 Her-2. The biological effects of this method inhibiting the proliferation and growth of tumor cells are much larger than only acting on one target. The combination of Lapatinib with Capecitabine is used to treat patients with advanced or metastatic breast cancer with overexpression of human epidermal receptor2, already treated with anthracyclines, paclitaxel, and trastuzumab. Clinical trials have shown that Lapatinib also effectively treats HER2-type cancer patients with Herceptin resistance.

Mechanisms of Action

Lapatinib is a tyrosine kinase inhibitor which can effectively inhibit the tyrosine kinase activity of human epidermal growth factor receptors 1 and 2 (ErbB1, ErbB2). It can uniquely act in a variety of ways, ensuring that breast cancer cells cannot receive growth signals. It inhibits intracellular EGFR (ErbB-1) and HER2 (ErbB-2) ATP sites, preventing tumor cell phosphorylation and activation, blocking down-regulation signals through the homogeneity and heterogeneity of EGFR (ErbB-1) and HER2 (ErbB-1) dimerization.

Description

Lapatinib, a new member of the 4-anilinoquinazoline class of RTK inhibitors (RTKIs), was launched as an oral treatment for breast cancer. Lapatinib has dual affinity for EGFR and HER2 tyrosine kinases. It is indicated in combination with capecitabine for treating patients with advanced or metastatic breast cancer whose tumors overexpress HER2 and who have received prior therapy including an anthracycline, a taxane, and trastuzumab. Previously marketed drugs from the 4-anilinoquinazoline class include erlotinib (Tarceva) and gefitinib (IressaTM), both of which are indicated for treating non-small-cell lung cancer (NSCLC). As with erlotinib and gefitinib, To Market, To Market 2007 475 lapatinib is an ATP-competitive kinase inhibitor. It inhibits the tyrosine kinase activity EGFR and HER-2 with apparent Ki values of 3 and 13 nM, respectively, and has slow off-rate kinetics (t1/2X300 min).
In addition, dividing the daily dose of lapatinib results in approximately 2-fold higher exposure at steady state compared to the same total dose administered once daily.
The chemical synthesis of lapatinib entails the condensation of 4-chloro-6-iodoquinazoline and 3-chloro-4-(3-fluorobenzyloxy)aniline to produce a diaryl amine intermediate followed by Stille coupling of the iodo group with 5-dioxolanyl-2-(tributylstannyl)furan and subsequent acid hydrolysis of the cyclic ketal to the corresponding aldehyde. Finally, reductive amination of the aldehyde intermediate with 2-(methanesulfonyl) ethylamine in the presence of sodium triacetoxyborohydride produces lapatinib. .

Originator

GSK (US)

Uses

Lapatinib, used in the form of Lapatinib Ditosylate, is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM, respectively. It is a antineoplastic which is used in breast cancer research and a tyrosine kinase inhibitor. It is used for the treatment of patients with advanced or metastatic breast cancer whose tumors overexpress HER2 (ErbB2)

Definition

ChEBI: Lapatinib is an organofluorine compound, an organochlorine compound, a member of quinazolines and a member of furans. It has a role as an antineoplastic agent and a tyrosine kinase inhibitor. It is functionally related to a monofluorobenzene.

brand name

Tykerb

target

EGFR

storage

Store at -20°C

References

1) Wood?et al. (2004),?A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells;? Cancer Res.,?64?6652 2) Burris?et al. (2004),?Dual kinase inhibition in the treatment of breast cancer: initial experience with the EGFR/ErbB-2 inhibitor lapatinib;? Oncologist,?9?10 3) Chu?et al. (2005),?The dual ErbB1/ErbB2 inhibitor, lapatinib (GW572016) cooperates with tamoxifen to inhibit both cell proliferation- and estrogen-dependent gene expression in antiestrogen-resistant breast cancer;? Cancer Res.,?65?18

1227853-06-6
231277-92-2
Synthesis of Lapatinib from 1227853-06-6
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Related articles

View Lastest Price from Lapatinib manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Lapatinib pictures 2024-03-16 Lapatinib
231277-92-2
US $35.00-25.00 / kg 1kg 99.8% 200tons/year Sigma Audley
lapatinib pictures 2023-12-29 lapatinib
231277-92-2
US $0.00-0.00 / kg 1kg 99%,single impurity<0.1 1 ton Nanjing Fred Technology Co., Ltd
Lapatinib pictures 2023-10-09 Lapatinib
231277-92-2
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
  • Lapatinib pictures
  • Lapatinib
    231277-92-2
  • US $35.00-25.00 / kg
  • 99.8%
  • Sigma Audley
  • lapatinib pictures
  • lapatinib
    231277-92-2
  • US $0.00-0.00 / kg
  • 99%,single impurity<0.1
  • Nanjing Fred Technology Co., Ltd
  • Lapatinib pictures
  • Lapatinib
    231277-92-2
  • US $0.00 / kg
  • 0.99
  • Hebei Yanxi Chemical Co., Ltd.

Lapatinib Spectrum

lapatinib n-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]-2-furyl]quinazolin-4-amine 4-Quinazolinamine, N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furanyl]- Lapatinib(TINIBS) Lapatinib Base N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furanyl]-4-Quinazolinamine GW2016 LAPATINIB N-(3-chloro-4-((3-fluorobenzyl)oxy)phenyl)-6-(5-(((2-(methylsulfonyl)ethyl)amino)methyl)furan-2-yl)quinazolin-4-amine N-{3-chloro-4-[(3-fluorobenzyl)oxyl]phenyl}-6-[5-({[2-(methylsulfonyl)ethyl]amino}methyl)furan-2-yl]quinazolin-4-amine GW-2016 Tyverb 4-[[3-Chloro-4-(3-fluorobenzyloxy)phenyl]aMino]-6-[5-[[(2-Methanesulfonylethyl)aMino]Methyl]furan-2-yl]quinazoline Lapatinib Ditosylate (API) 4-[[3-Chloro-4-(3-fluorobenzyloxy)phenyl]amino]-6-[5-[[(2-methanesulfonylethyl)amino]methyl]furan-2-yl]quinazoline GSK572016 GW 57201 N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furanyl]-4-quinazolinamine N-{3-chloro-4-[(3-fluorophenyl)Methoxy]phenyl}-6-(5-{[(2-Methanesulfonylethyl)aMino]Methyl}furan-2-yl)quinazolin-4-aMine N-{3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2-(Methanesulphonyl)ethyl]aMino}Methyl)-furan-2-yl]-4-quinazolinaMine Lapatinib (2TsOH) Lapatinib, 99+% GW-572016 GW-572016; TYKERB Lapatinib free base Lapatinib(GSK572016) Lapatinib N-[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]-2-furyl]quinazolin-4-amine N-[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]-2-furyl]quinazolin-4-amine Lapatinib Lapatinib(ditosylate salt) GW572016;GW-572016;GW 572016 CS-220 Lapatinib (GW572016, Tykerb) CS-1860 N-[3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl]-6-[5-[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine Lapatinib USP/EP/BP Lapatinib (GW-572016, Tykerb, Tyverb) N-[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]-2-furyl]quinazolin-4-amine LapatinibQ: What is Lapatinib Q: What is the CAS Number of Lapatinib Q: What is the storage condition of Lapatinib Q: What are the applications of Lapatinib TIANFUCHEM--231277-92-2-- Lapatinib in stock Tykerb Tyverb 1,10-Phenanthroline-5,10-dione Rapatini Rapatinib base 2H4]-Lapatinib 231277-92-2 31277-92-2 C29H26ClFN4O4S Inhibitors Anti-cancer&immunity Lapatinib APIs API Pharmaceutical intermediate anti-neoplastic Molecular Targeted Antineoplastic 231277-92-2