ChemicalBook--->CAS DataBase List--->10161-87-2

10161-87-2

10161-87-2 Structure

10161-87-2 Structure
IdentificationBack Directory
[Name]

Benzoic acid,4-[4-[(2-bromoacetyl)amino]butyl]-
[CAS]

10161-87-2
[Synonyms]

KRA-533
Benzoic acid,4-[4-[(2-bromoacetyl)amino]butyl]-
KRA-533,Benzoic acid,4-[4-[(2-bromoacetyl)amino]butyl]-
[Molecular Formula]

C13H16BrNO3
[MOL File]

10161-87-2.mol
[Molecular Weight]

314.17
Chemical PropertiesBack Directory
[Boiling point ]

530.4±45.0 °C(Predicted)
[density ]

1.428±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

4.34±0.10(Predicted)
[color ]

White to off-white
[InChI]

1S/C13H16BrNO3/c14-9-12(16)15-8-2-1-3-10-4-6-11(7-5-10)13(17)18/h4-7H,1-3,8-9H2,(H,15,16)(H,17,18)
[InChIKey]

WZQJLTLURXNPQG-UHFFFAOYSA-N
[SMILES]

O=C(O)C1=CC=C(CCCCNC(CBr)=O)C=C1
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

KRA-533 is a potent KRAS agonist. KRA-533 binds to the GTP/GDP binding pocket in the KRAS protein to prevent GTP cleavage, resulting in the accumulation of constitutively active GTP-bound KRAS that triggers both apoptotic and autophagic cell death pathways in cancer cells.
[Biological Activity]

KRA-333 is a potent and selective KRAS agonist th at binds directly to the GTP/GDP binding pocket of KRAS preventing the cleavage of GTP into GDP and caucusing accumulation of activated GTP-KRAS and suppression of cell growth. KRA-333 promotes apoptosis and autophagic cell death of cancer cells and inhibits growth of mutant KRAS lung cancer in xenografts mice model.
[in vivo]

KRA-533 (0~30 mg/kg; i.p.; 28 days) suppresses tumor growth in a dose-dependent manner in lung cancer mutant KRAS xenografts and induces apoptosis and autophagy in tumor tissues in a dose-dependent manner[1].
? KRA-533 shows optimal therapeutic index between 7.5 mg/kg and 30 mg/kg doses[1].

Animal Model:Nu/Nu nude mice (mutant KRAS xenografts)[1]
Dosage:0~30 mg/kg
Administration:i.p.; 28 days
Result:Suppressed tumor growth in a dose-dependent manner in lung cancer mutant KRAS xenografts and induced apoptosis and autophagy in tumor tissues in a dose-dependent manner.
[References]

[1] Xu K, et al. Small Molecule KRAS Agonist for Mutant KRAS Cancer Therapy [published correction appears in Mol Cancer. 2020 May 20;19(1):93]. Mol Cancer. 2019;18(1):85. Published 2019 Apr 10. DOI:10.1186/s12943-019-1012-4
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