ChemicalBook--->CAS DataBase List--->2460249-19-6

2460249-19-6

2460249-19-6 Structure

2460249-19-6 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2460249-19-6
[Synonyms]

PF-07104091
[Molecular Formula]

C19 H28 N6 O4
[MDL Number]

MFCD34471025
[MOL File]

2460249-19-6.mol
[Molecular Weight]

404.47
Chemical PropertiesBack Directory
[Boiling point ]

567.0±50.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: Sparingly soluble: 1-10 mg/ml
Ethanol: Sparingly soluble: 1-10 mg/ml
[pka]

12.51±0.46(Predicted)
[InChIKey]

MTNBRBDFNSGQKB-DCHPQEBHNA-N
[SMILES]

N(C1NN=C([C@H]2CC[C@@H](OC(=O)NC(C)C)C2)C=1)C(C1N(N=C(COC)C=1)C)=O |&1:5,8,r|
Questions And AnswerBack Directory
[Uses]

PF-07104091 can be used to treat advanced solid tumors, especially hormone receptor-positive (HR+)/HER2-negative breast cancer that is resistant to CDK4/6 inhibitors.
Hazard InformationBack Directory
[Description]

PF-07104091 is an inhibitor of cyclin-dependent kinase 2 (Cdk2; Ki = 1.16 nM).1 It is selective for Cdk2 over glycogen synthase kinase 3β (GSK3β; Ki = 537.81 nM). PF-07104091 decreases proliferation of TOV-21G and OVCAR-3 ovarian and HCT116 colorectal cancer cells (IC50s = 4.8, 0.59, and 0.88 µM, respectively).2 In vivo, PF-07104091 (50 mg/kg per day) reduces tumor volume and weight in an HCT116 mouse xenograft model.WARNING This product is not for human or veterinary use.
[storage]

Store at -20°C
[References]

[1] JUN TANG . Anilinopyrazole as selective CDK2 inhibitors[J]. Bioorganic & Medicinal Chemistry Letters, 2003, 13 18: Pages 2985-2988. DOI: 10.1016/s0960-894x(03)00630-9
[2] LIU Z, YANG Y, SUN X, et al. Discovery of Novel Antitumor Small-Molecule Agent with Dual Action of CDK2/p-RB and MDM2/p53[J]. Molecules, 2024, 33 1. DOI: 10.3390/molecules29030725
Spectrum DetailBack Directory
[Spectrum Detail]

PF-07104091(2460249-19-6)1HNMR
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