1. Others Apoptosis Metabolic Enzyme/Protease Immunology/Inflammation NF-κB
  2. Fluorescent Dye Photosensitizer Apoptosis Reactive Oxygen Species (ROS) SOD
  3. IR-775 chloride

IR-775 chloride is a cyanine dye with near-infrared absorption (Ex/Em = 775/795 nm). IR-775 chloride acts as a photosensitizer or photothermal agent, and induces apoptosis via generating ROS or exerting photothermal effects upon irradiation; its combination with 2-methoxyestradiol (HY-12033) inhibits SOD2 to enhance photodynamic therapy (PDT) efficacy, and its liposomal encapsulation enables phytotherapy-photothermal therapy (PTT) synergy. IR-775 chloride is applicable for investigating PDT/PTT and near-infrared fluorescence imaging in ovarian cancer and breast cancer.

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

IR-775 chloride

IR-775 chloride Chemical Structure

CAS No. : 199444-11-6

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

IR-775 chloride is a cyanine dye with near-infrared absorption (Ex/Em = 775/795 nm). IR-775 chloride acts as a photosensitizer or photothermal agent, and induces apoptosis via generating ROS or exerting photothermal effects upon irradiation; its combination with 2-methoxyestradiol (HY-12033) inhibits SOD2 to enhance photodynamic therapy (PDT) efficacy, and its liposomal encapsulation enables phytotherapy-photothermal therapy (PTT) synergy. IR-775 chloride is applicable for investigating PDT/PTT and near-infrared fluorescence imaging in ovarian cancer and breast cancer[1][2].

In Vitro

IR-775 (2-10 μM; 24-72 h) chloride is a potent photosensitizer in proliferative diabetic retinopathy (PDR). It reduces the viability of human ovarian adenocarcinoma cell line (SKOV-3) and human breast adenocarcinoma cell line (MDA-MB-231) in a time-dependent manner, and exhibits stronger cytotoxicity when combined with 2-methoxyestradiol plus irradiation[1].
IR-775 (6 μM; 2-24 h) chloride accumulates in non-nuclear organelles of human ovarian adenocarcinoma cell line (SKOV-3) and human breast adenocarcinoma cell line (MDA MB-231), and an increase in uptake is observed during the 2 h to 24 h incubation period[1].
IR-775 (6 μM; 24-72 h) chloride, when combined with 2-methoxyestradiol in a photodynamic reaction, induces oxidative stress and endoplasmic reticulum-mediated apoptosis in human ovarian adenocarcinoma cell line (SKOV-3) and human breast adenocarcinoma cell line (MDA MB-231), which is evidenced by altered SOD2 expression and increased caspase-12 expression after irradiation[1].
IR-775 (1 mg/mL) chloride can be efficiently encapsulated into spherical Hyptis suaveolens-IR-775-Liposome (HIL) NPs (141 nm), with an encapsulation efficiency of 69.13% and a drug loading rate of 17.29%. These nanoparticles exhibit characteristic near-infrared absorption/emission properties and degrade upon near-infrared laser irradiation[2].
The system of HIL nanoparticles loaded with IR-775 chloride exhibits high intracellular uptake efficiency in 4T1 cells. After irradiation with an 808 nm NIR laser, it induces significant reactive oxygen species (ROS) production, and causes over 85% of 4T1 cell death through a synergistic photothermal-photodynamic effect (CI = 0.6)[2].
HIL-loaded nanoparticles with IR-775 chloride induce > 85% cell death in 4T1 three-dimensional spheroids under 808 nm NIR laser irradiation, and can deeply penetrate into the tumor core[2].
HIL NPs loaded with IR-775 chloride disrupt the mitochondrial membrane potential of 4T1 cells, accumulate in lysosomes, and upregulate γ-H2AX, Cathepsin B, and p53 under 808 nm NIR laser irradiation, thereby inducing DNA damage and apoptosis[2].

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

Cell Viability Assay[1]

Cell Line: human ovarian adenocarcinoma (SKOV-3), human breast adenocarcinoma (MDA MB-231)
Concentration: 2 μM; 4 μM; 6 μM; 8 μM; 10 μM
Incubation Time: 24 h (pre-incubation); 24 h (post-irradiation incubation); 72 h (post-irradiation incubation)
Result: Reduced viability in both cell lines when treated with 2-10 μM for 24 h.
Identified 6 μM as the non-toxic dose.
Reduced MDA MB-231 viability to ~80% and SKOV-3 viability to ~88% after 24 h post-irradiation incubation when used alone in photodynamic reaction (PDR).
Reduced MDA MB-231 viability to 53% after 24 h and 33% after 72 h post-irradiation incubation, and SKOV-3 viability to 60% after 24 h and 45% after 72 h post-irradiation incubation when combined with 2-methoxyestradiol and irradiation.
Showed minimal cytotoxicity alone without irradiation.

Immunofluorescence[1]

Cell Line: human ovarian adenocarcinoma (SKOV-3), human breast adenocarcinoma (MDA MB-231)
Concentration: 6 μM
Incubation Time: 24 h (pre-incubation); 24 h (post-irradiation incubation); 72 h (post-irradiation incubation)
Result: Reduced SOD2 positive staining to 30% (weak intensity) at 24 h post-irradiation and 50% (weak intensity) at 72 h post-irradiation, while increasing caspase-12 positive staining to 80% (strong intensity) at both 24 h and 72 h post-irradiation in SKOV-3 cells.
Reduced SOD2 positive staining to 25% (moderate intensity) at 24 h post-irradiation, which returned to 100% (weak intensity) at 72 h post-irradiation, while increasing caspase-12 positive staining to 25% (weak-moderate intensity) at 24 h post-irradiation and 100% (strong intensity) at 72 h post-irradiation in MDA MB-231 cells.
Showed minimal caspase-12 staining and full SOD2 staining in unirradiated controls of both cell lines.
In Vivo

HIL NPs containing IR-775 chloride exhibit excellent biocompatibility and efficient uptake in healthy zebrafish embryos, with a strong fluorescence signal detected at 24 hours post-incubation[2].

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

Molecular Weight

519.55

Formula

C32H36Cl2N2

CAS No.
SMILES

CC1(C)C(/C=C/C2=C(Cl)/C(CCC2)=C/C=C3N(C)C4=C(C=CC=C4)C/3(C)C)=[N+](C)C5=C1C=CC=C5.[Cl-]

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:
IR-775 chloride
Cat. No.:
HY-W248590
Quantity:
MCE Japan Authorized Agent: