[CAS NO. 2254693-15-5]  SRX3207

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PRODUCTS SPECIFICATIONS [2254693-15-5]

Catalog
HY-136198
Brand
MCE
CAS
2254693-15-5

DESCRIPTION [2254693-15-5]

Overview

MDL-
Molecular Weight555.65
Molecular FormulaC29H29N7O3S
SMILESO=C1C2=C(C(C3=CC=C(NC4=NC=CC(N5N=C(C)C(CN6CCC6)=C5)=N4)C=C3)=CS2)OC(N7CCOCC7)=C1

For research use only. We do not sell to patients.

Summary

SRX3207 is an orally active and first-in-class dual Syk/PI3K inhibitor, with IC 50 values of 10.7 nM and 861 nM for Syk and PI3Kα , respectively. SRX3207 relieves tumor immunosuppression [1] [2] .


IC50 & Target

Syk

10.7 nM (IC 50 )

PI3Kα

861 nM (IC 50 )

PI3Kδ

1280 nM (IC 50 )

PI3Kγ

11100 nM (IC 50 )

Zap70

1300 nM (IC 50 )


In Vitro

SRX3207 (10 μmol/L) is able to block p-AKT at concentration [1] .
SRX3207 has sufficient solubility in water (43 μmol/L) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

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

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: LLC or B16 or B16-OVA or CT26 (1 × 10 5 ) 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.

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

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

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.7997 mL 8.9985 mL 17.9969 mL
5 mM 0.3599 mL 1.7997 mL 3.5994 mL
10 mM --- --- ---
* Please refer to the solubility information to select the appropriate solvent.