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Chemical Structure| 1903008-80-9 Chemical Structure| 1903008-80-9

Structure of Lazertinib
CAS No.: 1903008-80-9

Chemical Structure| 1903008-80-9

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Lazertinib is a selective inhibitor of mutant EGFR with lowest activity against EGFR wild type.

Synonyms: YH25448; GNS-1480

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Product Details of Lazertinib

CAS No. :1903008-80-9
Formula : C30H34N8O3
M.W : 554.64
SMILES Code : C=CC(NC1=CC(NC2=NC=CC(N3N=C(C4=CC=CC=C4)C(CN(C)C)=C3)=N2)=C(OC)C=C1N5CCOCC5)=O
Synonyms :
YH25448; GNS-1480
MDL No. :MFCD31728331
InChI Key :RRMJMHOQSALEJJ-UHFFFAOYSA-N
Pubchem ID :121269225

Safety of Lazertinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Related Pathways of Lazertinib

RTK
JAK-STAT

Isoform Comparison

Biological Activity

Target
  • EGFR/ErbB1

    WT EGFR, IC50:76 nM

    L858R/T790M EGFR, IC50:2 nM

  • mutant EGFR

    Del19/T790M, IC50:1.7 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
HEK293/ABCG2 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
HEK293/ABCB1 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
HEK293/Vector 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
S1-MI-80 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
S1 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
KBv200 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
KB 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
HepG2/adr 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
HepG2 0.25 μM 72 hours Evaluate the cytotoxicity of Lazertinib, approximately 90% of cells remained viable at 0.25 μM concentration PMC8897717
YU-1092 PDC (EGFR L861Q) 100 nM 24 hours To evaluate the antitumor activity of the combination of lazertinib and amivantamab in EGFR L861Q mutant PDC, results showed that the combination significantly suppressed the expression of pEGFR/tEGFR and pMET/tMET. PMC11866483
YUO-139 PDO (EGFR G719S) 10 nM 24 hours To evaluate the antitumor activity of the combination of lazertinib and amivantamab in EGFR G719S mutant PDO, results showed that the combination significantly suppressed the expression of pEGFR/tEGFR and tMET. PMC11866483
Ba/F3 cells (EGFR G719A/S768I) 100 nM 72 hours To evaluate the antitumor activity of the combination of lazertinib and amivantamab in EGFR G719A/S768I mutant cells, results showed that the combination significantly reduced the phosphorylation of EGFR (pEGFR). PMC11866483
Ba/F3 cells (EGFR S768I) 100 nM 72 hours To evaluate the antitumor activity of the combination of lazertinib and amivantamab in EGFR S768I mutant cells, results showed that the combination significantly reduced the phosphorylation of EGFR (pEGFR). PMC11866483
Ba/F3 cells (EGFR G719S) 3 nM 72 hours To evaluate the antitumor activity of the combination of lazertinib and amivantamab in EGFR G719S mutant cells, results showed that the combination significantly reduced the phosphorylation of EGFR (pEGFR). PMC11866483
YU-1092 patient-derived cells (EGFR L861Q mutation) 10 nM 72 hours To evaluate the anti-proliferative effect of Lazertinib on EGFR L861Q mutant cells, results showed significant inhibition of cell viability. PMC11866483
YUO-139 patient-derived organoid (EGFR G719S mutation) 19.5 nM 10 days To evaluate the anti-proliferative effect of Lazertinib on EGFR G719S mutant organoids, results showed significant inhibition of organoid viability. PMC11866483
Ba/F3 cells (EGFR G719A/S768I mutation) 100 nM 72 hours To evaluate the anti-proliferative effect of Lazertinib on EGFR G719A/S768I mutant cells, results showed significant inhibition of cell viability. PMC11866483
Ba/F3 cells (EGFR S768I mutation) 100 nM 72 hours To evaluate the anti-proliferative effect of Lazertinib on EGFR S768I mutant cells, results showed significant inhibition of cell viability. PMC11866483
Ba/F3 cells (EGFR G719S mutation) 3 nM 72 hours To evaluate the anti-proliferative effect of Lazertinib on EGFR G719S mutant cells, results showed significant inhibition of cell viability. PMC11866483
KPP-03 cells 100 nmol/L 72 hours Evaluate the effect of Lazertinib on KPP-03 cell growth, showing partial inhibition. PMC11447890
H1975 cells 100 nmol/L 72 hours Evaluate the effect of Lazertinib on H1975 cell growth, showing partial inhibition. PMC11447890
HCC4011 cells 100 nmol/L 72 hours Evaluate the effect of Lazertinib on HCC4011 cell growth, showing partial inhibition. PMC11447890
PC-9 cells 100 nmol/L 72 hours Evaluate the effect of Lazertinib on PC-9 cell growth, showing partial inhibition but not complete suppression. PMC11447890
H1975 NSCLC cells 5 or 50 nM 2 hours Evaluate the inhibitory effect of Lazertinib on EGFR(L858R/T790M) phosphorylation, results showed Lazertinib was more effective than osimertinib and LN2057 in suppressing pY1068 PMC9743421

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Nude mice HepG2/adr cell xenograft model Oral 10 mg/kg Every 3 days, total 6 times Evaluate the reversal of ABCB1-mediated multidrug resistance by Lazertinib in vivo, results showed Lazertinib significantly reduced tumor size and weight PMC8897717
BALB/c nude mice Ba/F3 EGFRG719S xenograft model Oral 10 mg/kg Once daily for 27 days To evaluate the anti-tumor effect of Lazertinib in EGFR G719S mutant xenograft model, results showed a tumor growth inhibition (TGI) value of 26.3% with lazertinib monotherapy. PMC11866483
Nude mice PC-9 cell CDX model 3 mg/kg daily Continuous administration for 31 days Evaluate the effect of Lazertinib alone or in combination with ONO-7475 and S63845 on PC-9 cell CDX model, showing significant tumor growth inhibition and no tumor regrowth with triple therapy. PMC11447890

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT05277701 NSCLC PHASE2 UNKNOWN 2025-12-24 Yonsei University Health Syste... More >>m, Severance Hospital, Seoul, Korea, Republic of Less <<
NCT05742594 Healthy PHASE1 COMPLETED 2023-04-03 Celerion, Tempe, Arizona, 8528... More >>3, United States Less <<
NCT05701384 Lung Cancer Stage IV|EGFR T790... More >>M Less << PHASE2 UNKNOWN 2025-01-31 Samsung Medical Center, Seoul,... More >> MA, 06351, Korea, Republic of Less <<
NCT03046992 EGFR Gene Mutation PHASE1|PHASE2 UNKNOWN 2025-12-22 Chungbuk National University H... More >>ospital, Cheongju-si, Chungcheongbuk-do, 28644, Korea, Republic of|The Catholic University of Korea, Bucheon St. Mary's Hospital, Bucheon-si, Gyeonggi-do, 14647, Korea, Republic of|National Cancer Center, Goyang-si, Gyeonggi-do, 03080, Korea, Republic of|CHA Bundang Medical Center, CHA University, Seongnam-si, Gyeonggi-do, 13496, Korea, Republic of|Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, 13620, Korea, Republic of|The Catholic University of Korea, St. Vincent's Hospital, Suwon-si, Gyeonggi-do, 16247, Korea, Republic of|Gyeongsang National University Hospital, Jinju-si, Gyeongsangnam-do, 52727, Korea, Republic of|Inje University Haeundae Paik Hospital, Busan, 48108, Korea, Republic of|Gachon University Gil Medical Center, Incheon, 21565, Korea, Republic of|Seoul National University Hospital, Seoul, 03080, Korea, Republic of|Kangbuk Samsung Hospital, Seoul, 03181, Korea, Republic of|Asan Medical Center, Seoul, 05505, Korea, Republic of|Samsung Medical Center, Seoul, 06351, Korea, Republic of|SMG-SNU Boramae Medical Center, Seoul, 07061, Korea, Republic of|Severance Hospital, Seoul, Korea, Republic of|Ulsan University Hospital, Ulsan, 44033, Korea, Republic of Less <<
NCT05112952 Hepatic Impairment|Healthy PHASE1 COMPLETED 2022-07-11 CRS Clinical Research Services... More >> Kiel GmbH, Kiel, 24105, Germany|APEX GmbH, Munchen, 81241, Germany Less <<
NCT05896683 Healthy PHASE1 COMPLETED 2023-09-01 SGS Belgium NV, Edegem, 2650, ... More >>Belgium Less <<
NCT05377788 Metastatic Lung Non-Small Cell... More >> Carcinoma|EGFR T790M Less << UNKNOWN 2024-06-30 Samsung Medical Center, Seoul,... More >> 06351, Korea, Republic of Less <<
NCT05716672 Non-small Cell Lung Cancer NOT_YET_RECRUITING 2025-12-31 Inje University Busan Paik Hos... More >>pital, Busan, 47392, Korea, Republic of|Inje University Haeundae Paik Hospital, Busan, 48108, Korea, Republic of|Dong-A University Hospital, Busan, 49201, Korea, Republic of|Pusan National University Hospital, Busan, 49241, Korea, Republic of|Kosin University Gospel Hospital, Busan, 49267, Korea, Republic of|Kyungpook National University Chilgok Hospital, Daegu, 41404, Korea, Republic of|Kyungpook National University Hospital, Daegu, 41944, Korea, Republic of|Yeungnam University Medical Center, Daegu, 42415, Korea, Republic of|Daegu Catholic University Medical Center, Daegu, 42472, Korea, Republic of|Keimyung University Dongsan Medical Center, Daegu, 42601, Korea, Republic of|Pusan National University Yangsan Hospital, Yangsan, 50612, Korea, Republic of Less <<
NCT05338619 Non-small Cell Lung Cancer Sta... More >>ge III|EGFR Positive Non-small Cell Lung Cancer|Non-squamous Non-small-cell Lung Cancer Less << PHASE2 RECRUITING 2026-03-02 Kosin University Gospel Hospit... More >>al, Busan, Korea, Republic of|Keimyung University Dongsan Hospital, Daegu, Korea, Republic of|Kyungpook National University Medical Center, Daegu, Korea, Republic of|Chungnam National University Hospital, Daejeon, Korea, Republic of|Chonnam National University Hospital Hwasun Hospital, Gwangju, Korea, Republic of|Inha University Hospital, Incheon, Korea, Republic of|Pusan National University Yangsan Hospital, Pusan, Korea, Republic of|Asan Medical Center, Seoul, Korea, Republic of|Hanyang University Seoul Hospital, Seoul, Korea, Republic of|Koera University Guro Hospital, Seoul, Korea, Republic of|Korea University Anam Hospital, Seoul, Korea, Republic of|Kyung Hee University Hospital, Seoul, Korea, Republic of|Yonsei University Health System, Severance Hospital, Seoul, Korea, Republic of Less <<
NCT04075396 Carcinoma, Non-Small-Cell Lung PHASE1|PHASE2 COMPLETED 2022-11-14 City of Hope, Duarte, Californ... More >>ia, 91010, United States|Advent Health Orlando, Orlando, Florida, 32804, United States|Moffitt Cancer Center, Tampa, Florida, 33612, United States|Montefiore Medical Center, Bronx, New York, 10461, United States|Tennessee Oncology, Nashville, Tennessee, 37211, United States|Hosp Univ Vall D Hebron, Barcelona, 8035, Spain|Hosp. Gral. Univ. Gregorio Maranon, Madrid, 28009, Spain|Hosp Virgen de La Victoria, Malaga, 29010, Spain|The Christie Nhs Foundation Trust, Manchester, M20 4BX, United Kingdom Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.80mL

0.36mL

0.18mL

9.01mL

1.80mL

0.90mL

18.03mL

3.61mL

1.80mL

References

 

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