1. Others Apoptosis Autophagy
  2. Fluorescent Dye Apoptosis Autophagy
  3. HJTA

HJTA is a selective, pH/GSH dual-responsive Fluorescent probe and anticancer agent. HJTA selectively undergoes an enzymatic reaction with GSTπ. HJTA induces Apoptosis and Autophagy by regulating the expression of apoptotic and autophagic proteins. HJTA exhibits pH- and GSH-dual-responsive fluorescence in tumor cells. HJTA selectively illuminates tumor tissues, enabling precise in situ visualization of colon tumors. HJTA exerts anticancer effects against colon cancer. HJTA can be used for colon cancer research.

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

HJTA

HJTA Chemical Structure

CAS No. : 2442502-32-9

Size Stock
50 mg   Get quote  
100 mg   Get quote  
250 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

HJTA is a selective, pH/GSH dual-responsive Fluorescent probe and anticancer agent. HJTA selectively undergoes an enzymatic reaction with GSTπ. HJTA induces Apoptosis and Autophagy by regulating the expression of apoptotic and autophagic proteins. HJTA exhibits pH- and GSH-dual-responsive fluorescence in tumor cells. HJTA selectively illuminates tumor tissues, enabling precise in situ visualization of colon tumors. HJTA exerts anticancer effects against colon cancer. HJTA can be used for colon cancer research[1].

In Vitro

HJTA potently inhibits the proliferation of HT29, HepG2 and 9L-2 cancer cells[1].
HJTA (0.4-2.5 μM; 72 h) induces apoptosis in colon cancer HT29 cells in a dose-dependent manner, and its mechanism of action involves upregulating Bax, downregulating Bcl-2, and activating caspase-3 and PARP[1].
HJTA (0.4-2.5 μM) induces autophagy in colon cancer cells HT29 in a dose-dependent manner, which is characterized by increased levels of LC3-II and Beclin-1, decreased level of p62, and elevated LC3-II/LC3-I ratio[1].

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

Apoptosis Analysis[1]

Cell Line: HT29 human colon cancer cells
Concentration: 0.4-2.5 μM
Incubation Time: 72 h
Result: Induced apoptotic cell percentages of 36.8% (1.0 μM), and 52.3% (2.5 μM).
Increased pro-apoptotic Bax levels dose-dependently.
Decreased anti-apoptotic Bcl-2 levels dose-dependently.
Increased levels of cleaved caspase-3 and cleaved PARP dose-dependently.
In Vivo

HJTA (20-40 mg/kg; i.p.; daily; 21 days) exhibits potent in vivo colon cancer xenograft growth inhibition, with the 40 mg/kg (i.p., daily for 21 days) dose reducing tumor weight by 67.7% relative to controls[1].

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

Animal Model: BALB/c nude (female, 5−6 weeks old)[1]
Dosage: 20 mg/kg; 40 mg/kg
Administration: i.p.; daily; 21 days
Result: Reduced mean tumor weight by 67.7% (40 mg/kg group) relative to the control group.
Significantly reduced tumor volume growth over the 21-day period relative to the control group, with the 40 mg/kg dose showing greater tumor growth inhibition than the 20 mg/kg dose.
Showed no significant changes in body weight between HJTA-treated groups and the control group.
Animal Model: ICR (female)[1]
Dosage: 240.0 mg/kg; 300.0 mg/kg; 375.0 mg/kg; 468.8 mg/kg; 585.9 mg/kg
Administration: i.p.; single dose
Result: Achieved 100% survival over 14 days with no abnormalities in body weight, eating, drinking, or activity in the 240.0 mg/kg and 300.0 mg/kg groups.
Achieved 80% survival with 2 deaths occurring by day 4 in the 375.0 mg/kg group.
Achieved 40% survival with 6 deaths occurring by day 4 in the 468.8 mg/kg group.
Achieved 10% survival with 9 deaths occurring by day 14 in the 585.9 mg/kg group.
Had a calculated median lethal dose (LD50) of 475 mg/kg.
Molecular Weight

501.53

Formula

C28H27N3O6

CAS No.
SMILES

O=C1C(COC(NC2=CC3=C(NC4=CC=CC=C43)C(C5=CC(OC)=C(C(OC)=C5)OC)=N2)=O)=CCCC1

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
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
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.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
HJTA
Cat. No.:
HY-D3211
Quantity:
MCE Japan Authorized Agent: