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Tinengotinib Aurora Kinase inhibitor

Cat.No.E1435

Tinengotinib (TT-00420) is a novel multiple kinase inhibitor that strongly inhibits Aurora A/B with IC50 values of 1.2/3.3 nM respectively. It also exhibits potent inhibitory activity on FGFR1/2/3, VEGFR1, JAK1/2, and CSF1R and can be used to treat several prominent signaling pathways in triple-negative breast cancer(TNBC).
Tinengotinib Aurora Kinase inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 394.86

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Quality Control

Batch: E143501 DMSO]79 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 99.07%
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99.07

Solubility

In vitro
Batch:

DMSO : 79 mg/mL (200.07 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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Chemical Information, Storage & Stability

Molecular Weight 394.86 Formula

C20H19ClN6O

Storage (From the date of receipt)
CAS No. 2230490-29-4 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
Aurora A
1.2 nM
Aurora B
3.3 nM
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04919642 Completed
Cholangiocarcinoma|FGFR2 Fusion|FGFR2 Gene Mutation|FGFR1 Alteration|FGFR3 Alteration
TransThera Sciences (Nanjing) Inc.
December 7 2021 Phase 2
NCT04705922 Completed
Healthy
TransThera Sciences (Nanjing) Inc.
December 29 2020 Phase 1
NCT03654547 Active not recruiting
Advanced Solid Tumors|Triple Negative Breast Cancer
TransThera Sciences (Nanjing) Inc.
January 8 2019 Phase 1

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