ChemicalBook--->CAS DataBase List--->2254693-15-5

2254693-15-5

2254693-15-5 Structure

2254693-15-5 Structure
IdentificationBack Directory
[Name]

7H-Thieno[3,2-b]pyran-7-one, 3-[4-[[4-[4-(1-azetidinylmethyl)-3-methyl-1H-pyrazol-1-yl]-2-pyrimidinyl]amino]phenyl]-5-(4-morpholinyl)-
[CAS]

2254693-15-5
[Synonyms]

SRX3207
7H-Thieno[3,2-b]pyran-7-one, 3-[4-[[4-[4-(1-azetidinylmethyl)-3-methyl-1H-pyrazol-1-yl]-2-pyrimidinyl]amino]phenyl]-5-(4-morpholinyl)-
[Molecular Formula]

C29H29N7O3S
[MDL Number]

MFCD33402171
[MOL File]

2254693-15-5.mol
[Molecular Weight]

555.65
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 5 mg/mL (9.00 mM; Need ultrasonic)
[form ]

Solid
[color ]

Light yellow to light brown
Hazard InformationBack Directory
[Uses]

SRX3207 is an orally active and first-in-class dual Syk/PI3K inhibitor, with IC50 values of 10.7 nM and 861 nM for Syk and PI3Kα, respectively. SRX3207 relieves tumor immunosuppression[1][2].
[Biological Activity]

SRX3207 is an orally active and first-in-class dual Syk/PI3K inhibitor, with IC50 values of 10.7 nM and 861 nM for Syk and PI3Kα, respectively. SRX3207 relieves tumor immunosuppression[1][2]. SRX3207 (10 μmol/L) is able to block p-AKT at concentration[1].SRX3207 has sufficient solubility in water (43 μmol/L)[1]. SRX3207 (10 mg/kg, orally) increases antitumor immune response[1].
[in vivo]

SRX3207 (10 mg/kg, orally) increases antitumor immune response[1].

Animal Model:LLC or B16 or B16-OVA or CT26 (1 × 105) cells were injected subcutaneously into syngeneic mice[1].
Dosage:10 mg/kg.
Administration:Orally, starting from day 10 when tumors reached 100 mm3 until tumors were harvested on day 21.
Result:Blocked phosphorylation of Syk at 348 site and Y525/526 site.
Blocked immunosuppressive MΦ polarization.
Blocked tumor growth and increased survival effectively.
[IC 50]

Syk: 10.7 nM (IC50); PI3Kα: 861 nM (IC50); PI3Kδ: 1280 nM (IC50); PI3Kγ: 11100 nM (IC50); Zap70: 1300 nM (IC50)
[storage]

Store at -20°C
[References]

[1]. Shweta Joshi, et al. Macrophage Syk-PI3Kγ Inhibits Antitumor Immunity: SRX3207, a Novel Dual Syk-PI3K Inhibitory Chemotype Relieves Tumor Immunosuppression. Molecular Cancer Therapeutics. 2020. [2]. Shweta Joshi, et al. Macrophage Syk-PI3Kγ Inhibits Antitumor Immunity: SRX3207, a Novel Dual Syk-PI3K Inhibitory Chemotype Relieves Tumor Immunosuppression. Mol Cancer Ther. 2020 Mar;19(3):755-764.
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