1. Apoptosis Protein Tyrosine Kinase/RTK
  2. Apoptosis c-Met/HGFR PDGFR Src TAM Receptor
  3. Multi-kinase-IN-1

Multi-kinase-IN-1 (Compound 11k) is a potent kinase inhibitor with antitumor activity. Multi-kinase-IN-1 induces cell apoptosis, and can be studied for colorectal cancer.

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Multi-kinase-IN-1 Chemical Structure

Multi-kinase-IN-1 Chemical Structure

CAS No. : 2470807-67-9

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Description

Multi-kinase-IN-1 (Compound 11k) is a potent kinase inhibitor with antitumor activity. Multi-kinase-IN-1 induces cell apoptosis, and can be studied for colorectal cancer[1].

IC50 & Target

Ron

0.122 μM (IC50)

PDGFRα

0.384 μM (IC50)

c-Src

0.421 μM (IC50)

AXL

0.632 μM (IC50)

Cellular Effect
Cell Line Type Value Description References
HT-29 IC50
0.31 μM
Compound: 11k
Anticancer activity against human HT-29 cells assessed as inhibition of cell proliferation by MTT assay
Anticancer activity against human HT-29 cells assessed as inhibition of cell proliferation by MTT assay
[PMID: 32731184]
In Vitro

Multi-kinase-IN-1 (Compound 11k) (0-5 µg/mL, 0-72 h) induces antiproliferation and cytotoxicity in a dose- and time-dependent manner in HT-29 cells, and is much less toxic to normal colorectal mucosa epithelial cells[1].
Multi-kinase-IN-1 (0-3 µg/mL, 0-72 h) induces cell apoptosis in a time- and dose-dependent manner[1].
Multi-kinase-IN-1 (0-3 µg/mL, 48 h) slightly induces cell cycle arrest in G2/M phase[1].

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

Cell Proliferation Assay[1]

Cell Line: HT-29 (human colon cancer cell) and FHC (normal colorectal mucosa epithelial cells)
Concentration: 0.56, 1.67, and 5 µg/mL for HT-29, 10 µg/mL for FHC
Incubation Time: 0-72 h
Result: Led to significant cytotoxicity in a dose- and time-dependent manner in HT-29 cells. Showed low toxicity in FHC cells.

Apoptosis Analysis[1]

Cell Line: HT-29
Concentration: 0.3, 1, and 3 µg/mL
Incubation Time: 0-72 h
Result: Induced cell apoptosis in a time- and dose-dependent manner.

Cell Cycle Analysis[1]

Cell Line: HT-29
Concentration: 0.3, 1, and 3 µg/mL
Incubation Time: 48 h
Result: Slightly induced cell cycle arrest with a G2/M percentage of 4.4% at 3.0 mg/mL compared to 0.1% DMSO (2.4%).
Molecular Weight

706.76

Formula

C35H36F2N6O6S

CAS No.
SMILES

O=C(N1CCC(OC2=C(OC)C=C3C(OC4=CC=C(NC(NN5C(C6=C(F)C=CC=C6F)SCC5=O)=O)C=C4)=CC=NC3=C2)CC1)NC(C)C

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
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Multi-kinase-IN-1
Cat. No.:
HY-146014
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