MedKoo Cat#: 127040 | Name: BLU-451
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

BLU-451, also known as LNG-451, orally bioavailable, central nervous system (CNS) penetrating, mutant-selective covalent inhibitor of epidermal growth factor receptor (EGFR) exon 20 insertion (Ex20ins) activating mutations, with potential antineoplastic activity. Upon oral administration, EGFR Ex20ins inhibitor BLU-451 selectively targets, irreversibly binds to and inhibits the activity of EGFR Ex20ins and some other oncogenic point mutations. This prevents EGFR Ex20ins-mediated signaling. This may induce cell death and inhibit tumor growth in EGFR Ex20ins-overexpressing tumor cells. EGFR, a receptor tyrosine kinase mutated in many tumors, plays a key role in tumor cell proliferation and tumor vascularization. BLU-451 is able to penetrate the blood-brain-barrier (BBB) and may therefore exert its activity against EGFR Ex20ins-driven CNS primary tumors and CNS metastases. BLU-451 does not inhibit the activity of wild-type (WT) EGFR. EGFR Ex20ins are oncogenic driver mutations that constitutively upregulate kinase activity.

Chemical Structure

BLU-451
BLU-451
CAS#2769954-39-2

Theoretical Analysis

MedKoo Cat#: 127040

Name: BLU-451

CAS#: 2769954-39-2

Chemical Formula: C24H19F4N7O

Exact Mass: 497.1587

Molecular Weight: 497.46

Elemental Analysis: C, 57.95; H, 3.85; F, 15.28; N, 19.71; O, 3.22

Price and Availability

Size Price Availability Quantity
50mg USD 250.00 2 Weeks
100mg USD 450.00 2 Weeks
200mg USD 750.00 2 Weeks
500mg USD 1,650.00 2 Weeks
1g USD 2,950.00 2 Weeks
2g USD 5,250.00 2 Weeks
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Synonym
BLU-451; BLU451; BLU 451; LNG451; LNG 451; pebezertinibum; pebezertinib
IUPAC/Chemical Name
N-(4-fluoro-3-((2-((1-methyl-1H-pyrazol-4-yl)amino)-5-(4-(trifluoromethyl)phenyl)pyrimidin-4-yl)amino)phenyl)acrylamide
InChi Key
XIMJCWSFLXXQMZ-UHFFFAOYSA-N
InChi Code
InChI=1S/C24H19F4N7O/c1-3-21(36)31-16-8-9-19(25)20(10-16)33-22-18(14-4-6-15(7-5-14)24(26,27)28)12-29-23(34-22)32-17-11-30-35(2)13-17/h3-13H,1H2,2H3,(H,31,36)(H2,29,32,33,34)
SMILES Code
CN1C=C(C=N1)NC2=NC=C(C(=N2)NC3=C(C=CC(=C3)NC(=O)C=C)F)C4=CC=C(C=C4)C(F)(F)F
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Biological target:
EGFR inhibitor
In vitro activity:
BLU-451 in vitro and in vivo characterization was performed in a range of pharmacokinetic (PK) studies to assess brain penetration and to measure efflux ratios in cell lines over-expressing MDR1 and BCRP. Reference: Pearson, P. G., Pandey, A., Roth, B., Saxton, T., Estes, D. J., Trivedi, R., ... & Murray, B. W. (2022). LNG-451 (BLU-451), a potent inhibitor of EGFR exon 20 insertion mutations with high CNS exposure. AACR.
In vivo activity:
BLU-451 in vitro and in vivo characterization was performed in a range of pharmacokinetic (PK) studies to assess brain penetration and to measure efflux ratios in cell lines over-expressing MDR1 and BCRP. References: Pearson, P. G., Pandey, A., Roth, B., Saxton, T., Estes, D. J., Trivedi, R., ... & Murray, B. W. (2022). LNG-451 (BLU-451), a potent inhibitor of EGFR exon 20 insertion mutations with high CNS exposure. AACR.

Preparing Stock Solutions

The following data is based on the product molecular weight 497.46 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Zhou Y, Li J, Ying J. Anti-PD-1/L1 antibody plus anti-VEGF antibody vs. plus VEGFR-targeted TKI as first-line therapy for unresectable hepatocellular carcinoma: a network meta-analysis. Explor Target Antitumor Ther. 2024;5(3):568-580. doi: 10.37349/etat.2024.00236. Epub 2024 Jun 17. PMID: 38966165; PMCID: PMC11220314.