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SRX3177 CDK inhibitor

Cat.No.E4702

SRX3177 is a potent triple inhibitor targeting CDK4/6, PI3K, and BRD4, with IC50 values of 33 nM for BRD4 BD1, 89 nM for BRD4 BD2, 79 nM for PI3Kα, 83 nM for PI3Kδ, 3.18 μM for PI3Kγ, <2.5 nM for CDK4, and 3.3 nM for CDK6. By simultaneously inhibiting these key pathways, this compound disrupts cancer cell signalling and exhibits significant cytotoxic effects in tumors.
SRX3177 CDK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 584.69

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Quality Control

Batch: E470201 DMSO]25 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 97.41%
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  • NMR
  • HPLC
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  • Datasheet
97.41

Solubility

In vitro
Batch:

DMSO : 25 mg/mL (42.75 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Chemical Information, Storage & Stability

Molecular Weight 584.69 Formula

C31H32N6O4S

Storage (From the date of receipt)
CAS No. 2241237-51-2 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
CDK4
<2.5 nM
CDK6
3.3 nM
BRD4 BD1
33 nM
PI3Kα
79 nM
PI3Kδ
83 nM
BRD4 BD2
89 nM
PI3Kγ
3.18 μM
References

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