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Chemical Structure| 388082-78-8 Chemical Structure| 388082-78-8

Structure of 388082-78-8

Chemical Structure| 388082-78-8

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Lapatinib ditosylate monohydrate (GW572016 ditosylate monohydrate) is a potent inhibitor of the ErbB-2 and EGFR tyrosine kinase domains with IC50 values of 10.2 nM and 9.8 nM against purified EGFR and ErbB-2, respectively.

Synonyms: GW2016 ditosylate monohydrate; GW572016 ditosylate monohydrate; Lapatinib tosilate hydrate

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Product Details of Lapatinib ditosylate monohydrate

CAS No. :388082-78-8
Formula : C43H44ClFN4O11S3
M.W : 943.48
SMILES Code : O=S(CCNCC1=CC=C(C2=CC3=C(NC4=CC=C(OCC5=CC=CC(F)=C5)C(Cl)=C4)N=CN=C3C=C2)O1)(C)=O.O=S(C6=CC=C(C)C=C6)(O)=O.O=S(C7=CC=C(C)C=C7)(O)=O.[H]O[H]
Synonyms :
GW2016 ditosylate monohydrate; GW572016 ditosylate monohydrate; Lapatinib tosilate hydrate
MDL No. :MFCD18904381

Safety of Lapatinib ditosylate monohydrate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Lapatinib ditosylate monohydrate

RTK
JAK-STAT

Isoform Comparison

Biological Activity

Description
Lapatinib ditosylate monohydrate (GW572016 ditosylate monohydrate) is a potent inhibitor targeting the tyrosine kinase domains of ErbB-2 and EGFR, demonstrating IC50 values of 9.8 nM and 10.2 nM against purified ErbB-2 and EGFR respectively[1].

In Vitro:

Cell Line
Concentration Treated Time Description References
BT474 cells 1 μM overnight Lapatinib inhibited FASN phosphorylation. PMC3046439
SKBR3 cells 1 μM 18 h Lapatinib inhibited EGFR and HER2 phosphorylation and led to dephosphorylation of FASN. PMC3046439
SKBR3 cells 10 nM 72 h To evaluate the effects of dual HER2 blockade on HER2-E breast cancer cell lines, results showed that SKBR3 cell line did not switch to Luminal A phenotype after treatment. PMC6971277
BT474 cells 10 nM 72 h To evaluate the effects of dual HER2 blockade on HER2-E breast cancer cell lines, results showed that BT474 cell line switched to Luminal A phenotype after treatment. PMC6971277
UACC893 cells 1 μM 72 h To evaluate the antiproliferative effect of lapatinib on HER2-amplified breast cancer cells. Results showed that lapatinib inhibited HER2 phosphorylation, but the inhibition of PI3K signaling was attenuated in PIK3CA-mutant cells. PMC3978602
HCC1954 cells 1 μM 72 h To evaluate the antiproliferative effect of lapatinib on HER2-amplified breast cancer cells. Results showed that lapatinib inhibited HER2 phosphorylation, but the inhibition of PI3K signaling was attenuated in PIK3CA-mutant cells. PMC3978602
MDA-MB-361 cells 1 μM 72 h To evaluate the antiproliferative effect of lapatinib on HER2-amplified breast cancer cells. Results showed that lapatinib inhibited HER2 phosphorylation, but the inhibition of PI3K signaling was attenuated in PIK3CA-mutant cells. PMC3978602
SKBR3 cells 1 μM 72 h To evaluate the antiproliferative effect of lapatinib on HER2-amplified breast cancer cells. Results showed that lapatinib inhibited HER2 phosphorylation, but the inhibition of PI3K signaling was attenuated in PIK3CA-mutant cells. PMC3978602
CD24HiCD49fHiLin− TIC-enriched cells 5 μM 10 min Inhibition of Nrg1-mediated activation of Akt and Erk1/2 PMC3917843
BT474 cells 1 μM 72 h To evaluate the antiproliferative effect of lapatinib on HER2-amplified breast cancer cells. Results showed that lapatinib inhibited HER2 phosphorylation, but the inhibition of PI3K signaling was attenuated in PIK3CA-mutant cells. PMC3978602
NUGC-4 cell lines 69 nM(GI50) 3 days Evaluate the anti-proliferative effect of Lapatinib on HER2-high gastric cancer cell lines, results showed NUGC-4 was sensitive to Lapatinib PMC3950883
NCI-N87 cell lines 16 nM(GI50) 3 days Evaluate the anti-proliferative effect of Lapatinib on HER2-high gastric cancer cell lines, results showed NCI-N87 was sensitive to Lapatinib PMC3950883
A375 melanoma cells 200nM 24 h To evaluate the inhibitory effect of Lapatinib alone or in combination with Phenformin on cell proliferation. The results showed that Lapatinib alone had a significant inhibitory effect on A375 cells, but the combination with Phenformin was more effective PMC7252493
NT2197 cells 600 nM 24 h To evaluate the inhibitory effect of Lapatinib alone or in combination with Phenformin on cell proliferation. The results showed that Lapatinib alone had a significant inhibitory effect on NT2197 cells, but the combination with Phenformin was more effective PMC7252493
SkBr3 1µM 48 h To evaluate the apoptotic response of HER2 amplified breast cancer cells to lapatinib. BIM knockdown significantly reduced lapatinib-induced apoptosis. PMC3229203
EFM-192A 1µM 72 h To evaluate the apoptotic response of HER2 amplified breast cancer cells to lapatinib. EFM-192A cells showed <5% apoptosis. PMC3229203
BT-474 1µM 72 h To evaluate the apoptotic response of HER2 amplified breast cancer cells to lapatinib. BT-474 cells showed ~65% apoptosis, while EFM-192A cells showed <5% apoptosis. PMC3229203

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
NOD/scid/Il2 γ-null (NSG) mice Breast cancer xenograft model Oral gavage 100 mg/kg 5 days/week To study the effect of lapatinib on HER2 blockade, results showed that lapatinib combined with other anti-HER2 therapy and anti-estrogen therapy led to rapid tumor regression to a non-palpable state. PMC8178846
Nude mice SGC031 PDGCX model Oral 100 mg/kg Twice daily for 3 weeks Evaluate the anti-tumor efficacy of Lapatinib in MET amplification and overexpression PDGCX model, results showed Lapatinib did not significantly inhibit tumor growth PMC3950883
NOD/SCID mice HER2-overexpressing breast cancer model Oral 100 mg/kg Once daily for 3 weeks To evaluate the efficacy of combined lapatinib and BYL719 treatment in HER2-positive breast cancer PMC8567053
Female athymic nude mice HER2-amplified xenograft model Lapatinib and BKM120: oral gavage; Trastuzumab: intraperitoneal injection 100 mg/kg Lapatinib and BKM120: daily; Trastuzumab: twice weekly; duration: 28 days To evaluate the antitumor effects of lapatinib, trastuzumab, and BKM120 alone or in combination on HER2-amplified xenografts. Results showed that in PIK3CA wild-type tumors, the combination of lapatinib and trastuzumab induced tumor regression, and the addition of BKM120 further improved tumor regression and reduced tumor relapse after treatment discontinuation. In PIK3CA-mutant tumors, the combination of lapatinib and trastuzumab failed to induce tumor regression, while the addition of BKM120 resulted in tumor regression. PMC3978602
Mice MMTV-Wnt-1 mammary tumor model Oral gavage 100 mg/kg Twice daily for 14 days Inhibition of tumor growth and TIC self-renewal PMC3917843
NOD SCID mice HT-29 colorectal tumor xenografts Oral 60 mg/kg Once daily for 10 days To study the effect of lapatinib on tumor growth in HT-29 colorectal tumor xenograft model. Results showed that lapatinib combined with sorafenib significantly inhibited tumor growth, and serum phospho-CSE1L levels declined 3 days after treatment. PMC4467675
Nude mice NT2197 xenograft model Phenformin via intraperitoneal injection, lapatinib via gavage 50mg/kg Every 24 hours for 8 days Evaluate the anti-tumor efficacy of Lapatinib and phenformin combination, showing significant inhibition of tumor growth PMC7252493
Nude mice HER2 amplified breast cancer xenograft model Oral gavage 100mg/kg Once daily for ~30 days To evaluate the anti-tumor effect of lapatinib in HER2 amplified breast cancer xenograft models. High BIM expressing BT-474 cells were more sensitive to lapatinib, while low BIM expressing ZR7530 cells showed weaker response. PMC3229203

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.06mL

0.21mL

0.11mL

5.30mL

1.06mL

0.53mL

10.60mL

2.12mL

1.06mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1

References

 

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