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Cat. No.: HY-123565

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TP-S1-68

TP-S1-68 (Compound 10) is a TIE-2 inhibitor with an IC₅₀ of 3.65 μM. TP-S1-68 exhibits antibacterial activity against a variety of fungal and bacteria. TP-S1-68 serves as a starting compound for the further development of TIE-2 inhibitors. TP-S1-68 can be used in research related to solid tumors, bacterial infections and fungal infections.

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

CAS No.: 120187-04-4
Formula: C₁₅H₉ClN₄S
Molecular Weight:312.78

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

TP-S1-68 Chemical Structure

CAS No.: 120187-04-4

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

IC₅₀ & Target^[1]

Tie2

3.65 μM (IC₅₀)

All Tie Isoforms :

Tie1
Tie2

In Vitro

TP-S1-68 inhibits the activity of purified recombinant human TIE-2 kinase with an IC₅₀ of 3.650 μM, and suppresses 101.62% of the kinase activity at a concentration of 5 μg/mL^[1].
TP-S1-68 (Compound 5a) exhibits antimicrobial activity against the bacteria Staphylococcus aureus (MTCC 3160), Staphylococcus epidermidis (MTCC 435), Bacillus cereus (MTCC 9786), Escherichia coli (MTCC 118), Klebsiella pneumoniae (MTCC 3384), Pseudomonas aeruginosa (MTCC 4673), and the fungi Candida albicans (MTCC 1637) and Aspergillus niger (MTCC 282), with MIC values of 6.25, 6.25, 6.25, 12.5, 12.5, 12.5, 6.25, and 6.25 μg/mL^[2].

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

Chemical Information

CAS No. 120187-04-4
Molecular Weight 312.78
Formula C₁₅H₉ClN₄S
SMILES

ClC=1C=CC(=CC1)C2=NN=C3SC(=NN32)C=4C=CC=CC4
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. Pan P, et al. Identification and Preliminary SAR Analysis of Novel Type-I Inhibitors of TIE-2 via Structure-Based Virtual Screening and Biological Evaluation in in vitro Models. J Chem Inf Model. 2015;55(12):2693-2704. [Content Brief]

[2]. Jagdish K. Sahu, et al. Synthesis, SAR and Molecular Docking Studies of Certain New Derivatives of 1,2,4-Triazolo [3,4-b][1,3,4] Thiadiazole as Potent Antimicrobial Agents. Anti-Infective Agents, 2018, 16, 40-48.

[3]. Shawali, A. S.,, et al.. Tandem regioselective 1,5-electrocyclizations of bis-nitrilimines—a new convenient synthesis of 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles. Journal of Sulfur Chemistry, 27(3), 233–244.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

100 mg

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