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Product Information:

BBO-10203

BBO-10203 is a potent inhibitor of PI3Kα and KRAS G12C, selectively and covalently binding to Cys242 in the RAS-Binding Domain of PI3Kα, and inhibiting both the GTP-bound and GDP-bound states of KRAS G12C with an IC50 of 0.031 nM and an EC50 of 0.02 nM. BBO-10203 disrupts the interaction between RAS isoforms and PI3Kα, leading to the inhibition of RAS-mediated PI3Kα activation, and reduces pERK expression, cell growth, and induces G1 arrest and apoptosis. BBO-10203 can be used for the research of breast cancer, colorectal cancer, and non-small cell lung cancer .

Cat. No.: EX-A12048    Purity: >98%
Chemical
Chemical structure of BBO-10203


For research only, Do not use for Human!

SizeUnit Price (US$)StockQuantityOrder
1mg400In-stock
5mg830In-stock
10mg1150In-stock
25mg1960In-stock
50mg2880In-stock
100mg4600In-stock


CAS No.2971769-60-3
Purity>98%
FormulaC34H30F2N6O3S
Mol Weight640.702
ColorWhite to off-white
StateSolid
SolubilitySoluble in DMSO
Shelf Life>3 years if stored properly
StoragePowder 4℃,protect from light, 2 years; In solvent -20℃ 1 month;
ShippingShipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
 
 
Reference:  

[1]. Fan Z, et al. Precise regulation of RAS-Mediated PI3Kα activation: therapeutic potential of BBO-10203 in cancer treatment. Exp Hematol Oncol. 2025;14(1):115. Published 2025 Sep 29.

[2]. Kerstin W. Sinkevicius, et al. Abstract C082: BBO-10203, a first-in-class, orally bioavailable, selective breaker of the RAS:PI3Kα interaction inhibits tumor growth alone and in combination with KRAS inhibitors in KRAS mutant models without inducing hyperglycemia. Mol Cancer Ther (2025) 24 (10_Supplement): C082.

CoACoA of BBO-10203
Smiles:O=C(C=C)N1CCN2N=C(C=C2C1C)C=3N=C(C=4C=CC5=C(C=NN5C)C4)C=6C=CSC6C3C7=C(F)C=C(F)C=C7OCCOC

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