Structure of Lazertinib
CAS No.: 1903008-80-9
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Lazertinib is a selective inhibitor of mutant EGFR with lowest activity against EGFR wild type.
Synonyms: YH25448; GNS-1480
4.5
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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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 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302 |
Precautionary Statements: | P280-P305+P351+P338 |
Target |
|
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 << |
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 |
Tags: Lazertinib | YH25448 | GNS-1480 | YH 25448 | YH-25448 | GNS1480 | GNS 1480 | GNS-1480 | EGFR | Epidermal growth factor receptor | ErbB-1 | HER1 | EGFR inhibitor | non-small cell lung cancer | EGFR mutation | EGFR ATP-binding site | 1903008-80-9
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H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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