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BI-2865

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CAS:2937327-93-8
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CAS:2937327-93-8
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Products Intro: Product Name:BI-2865
CAS:2937327-93-8
Purity:98%+ HPLC HNMR Package:10mg|50mg|100mg
Company Name: Nantong QuanYi Biotechnology Co., Ltd  Gold
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Products Intro: Product Name:BI-2865
CAS:2937327-93-8
Purity:98%+ HPLC Package:10mg;500mg;1g;5g;10ASSAYS

BI-2865 manufacturers

  • BI-2865
  • BI-2865 pictures
  • $222.00 / 1mg
  • 2025-11-10
  • CAS:2937327-93-8
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  • Purity: 99.39%
  • Supply Ability: 10g
  • BI-2865
  • BI-2865  pictures
  • $0.00 / 10mg
  • 2025-03-16
  • CAS:2937327-93-8
  • Min. Order: 5mg
  • Purity: 98%+ HPLC HNMR
  • Supply Ability: 20g
BI-2865 Basic information
Product Name:BI-2865
Synonyms:BI-2865;BI-2865, 10 mM in DMSO;(S)-2-Amino-4-methyl-4-[3-[4-[(S)-1-[(S)-1-methyl-2-pyrrolidinyl]ethoxy]-2-pyrimidinyl]-1,2,4-oxadiazol-5-yl]-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carbonitrile
CAS:2937327-93-8
MF:C23H27N7O2S
MW:465.57
EINECS:
Product Categories:
Mol File:2937327-93-8.mol
BI-2865 Structure
BI-2865 Chemical Properties
Boiling point 708.7±70.0 °C(Predicted)
density 1.38±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
form Solid
pka9.35±0.40(Predicted)
color Light yellow to brown
Safety Information
MSDS Information
BI-2865 Usage And Synthesis
DescriptionBI-2865 is a none-covalent pan-KRAS Inhibitor. BI-2865 blocked nucleotide exchange to prevent the activation of wild-type KRAS and a broad range of KRAS mutants, including G12A/C/D/F/V/S, G13C/D, V14I, L19F, Q22K, D33E, Q61H, K117N and A146V/T. Inhibition of downstream signaling and proliferation was restricted to cancer cells harboring mutant KRAS, and drug treatment suppressed KRAS mutant tumor growth in mice without having a detrimental effect on animal weight.
UsesBI-2865 is a none-covalent pan-KRAS Inhibitor. BI-2865 binds to WT, G12C, G12D, G12V and G13D mutant KRAS with KDs of 6.9, 4.5, 32, 26, 4.3 nM respectively. BI-2865 inhibits the proliferation of G12C, G12D or G12V mutant KRAS expressing BaF3 cells (mean IC50: roughly 140 nM)[1].
Biological ActivityBI-2865 is a non-covalent pan-KRAS inhibitor that binds to KRAS WT, G12C, G12D, G12V, and G13D mutants with Kd values of 6.9 nM, 4.5 nM, 32 nM, 26 nM, and 4.3 nM, respectively. It can be used in studies related to KRAS mutant tumors.
in vitro BI-2865 is a derivative with a prolinol substituent and a pyrimidine linker. BI-2865 has direct ionic interaction with E62 and a water-mediated hydrogen bond network with the side chain of R68 and the main chain carbonyl of Q61. BI-2865 (5 days) inhibits the proliferation of G12C, G12D, or G12V mutant KRAS expressing BaF3 cells in the presence of IL-13, with a mean IC50 of roughly 140?nM.
References[1] Kim D, et al. Pan-KRAS inhibitor disables oncogenic signalling and tumour growth. Nature. 2023 May 31. DOI:10.1038/s41586-023-06123-3
BI-2865 Preparation Products And Raw materials
Tag:BI-2865(2937327-93-8) Related Product Information
BI-2852 RMC-9805 RMC-7977 2-Propen-1-one, 1-[(3S)-4-[(7R)-7-[6-amino-4-methyl-3-(trifluoromethyl)-2-pyridinyl]-6-chloro-8-fluoro-2-[[(2S)-1-methyl-2-pyrrolidinyl]methoxy]-4-quinazolinyl]-3-methyl-1-piperazinyl]- MRTX1133 BI-2493 BI-3406 Adagrasib

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