GLPBio

HPPH

Catalog No.: GC33100Purity:>98.00%Synonyms: Photochlor, Pyropheophorbide-α-hexyl-ether, 2-1-hexyloxyethyl-2-devinyl Pyropheophorbide a

A photosentizer

Products are for research use only. Not for human use. We do not sell to patients.


HPPH
Cas No.: 149402-51-7
10mM (in 1mL DMSO)In Stock
$167.00
1
1mgIn Stock
$59.00
1
5mgIn Stock
$119.00
1
10mgIn Stock
$189.00
1
25mgIn Stock
$326.00
1

Citations

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    641, 529–536 (2025)
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    Nature
    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    387(6734) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Description

HPPH is a second-generation photosensitizer, which acts as a photodynamic therapy (PDT) agent. Fluorescence image of 4T1 cells incubated with 0.49 μg/mL GO-PEG, 1 μM HPPH (free HPPH) or equivalent amount of GO-PEG-HPPH (1 μM HPPH and 0.49 μg/mL GO-PEG) after 24 h. The cellular uptake of GO-PEG-HPPH and HPPH is investigated with 4T1 murine mammary cancer cells. The cells are incubated with GO-PEG-HPPH and free HPPH at equivalent HPPH concentration (1 μM) for 24 h and then observed with a confocal microscope. Cells treated with GO-PEG-HHPH show a stronger fluorescence signal than those treated with free HPPH. The fluorescence of HPPH is rather weak[1].

Tumors are treated with an immune-enhancing PDT regimen followed by a tumor-controlling PDT regimen can lead to enhancement of anti-tumor immunity, while retaining effective control of primary tumor growth. To test this hypothesis, a combination treatment regimen is devised in which Colo26-HA tumor-bearing BALB/c mice are treated with an HPPH-PDT regimen known to lead to enhanced anti-tumor immunity (0.4 μmoles/kg HPPH followed 18 h later by illumination with 665 nm light for a total dose of 48 J/cm2). Following illumination, mice are rested for 9 days; on the ninth day, mice are injected with HPPH. On day 10 following the first treatment, tumors are treated with a tumor control treatment regimen (illumination with 665 nm light for a total dose of 132 J/cm2 given)[2].

References:
[1]. Rong P, et al. Photosensitizer loaded nano-graphene for multimodality imaging-guided tumor photodynamic therapy. Theranostics. 2014 Jan 15;4(3):229-39.
[2]. Shams M, et al. Development of photodynamic therapy regimens that control primary tumor growth and inhibit secondary disease. Cancer Immunol Immunother. 2015 Mar;64(3):287-97.

Protocol

Cell experiment:

4T1 cells are cultured in 96-well cell culture plates at 1×104/well for 24 h and then treated with GO-PEG-HPPH, HPPH, or GO-PEG at a series of concentrations (0.078125, 0.15625, 0.3125, 0.625, 1.25, 2.5, 5, 10, and 20 μM). Then, 20 µL of MTT solution (5.0 mg/mL) is added to each well. After the 4 h incubation with the MTT, the media are removed and 100 µL of DMSO is added to solubilize the formazan crystals. The cell toxicity efficacy is measured with a microplate reader at an absorbance of 570 nm[1].

Animal experiment:

Mice[2]Tumor-bearing mice are injected in the tail vein with 0.4 μmol/kg HPPH or 5 mg/kg Porfimer sodium (PII), followed 18-24 h later by illumination to a total light dose of 48 J/cm2 or 132 J/cm2 delivered at a light dose-rate of 14 mW/cm2. Control mice are treated with photosensitizer or light alone. Mice receiving a combination PDT regimen are treated initially with 0.4 μmol/kg HPPH or 5 mg/kg PII followed 18-24 h later by light dose of 48 J/cm2 given at 14 mW/cm2; 9 days later, mice are again injected with photosensitizer and tumors are illuminated with light at a dose of 132 J/cm2 given at 14 mW/cm2[2].

References:

[1]. Rong P, et al. Photosensitizer loaded nano-graphene for multimodality imaging guided tumor photodynamic therapy. Theranostics. 2014 Jan 15;4(3):229-39.
[2]. Shams M, et al. Development of photodynamic therapy regimens that control primary tumor growth and inhibit secondary disease. Cancer Immunol Immunother. 2015 Mar;64(3):287-97.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
149402-51-7
Synonyms
Photochlor, Pyropheophorbide-α-hexyl-ether, 2-1-hexyloxyethyl-2-devinyl Pyropheophorbide a
SMILES
OC(CC[C@@H]([C@@H]1C)/C2=C(C3)/C4=C(C(C)=C(/C=C5C(CC)=C(C)C(/C=C6N/C(C(C)=C\6C(C)OCCCCCC)=C\C1=N2)=N/5)N4)C3=O)=O
Molecular Formula
C39H48N4O4
Molecular Weight
636.82
Solubility
DMSO: 125 mg/mL (196.29 mM); Water: < 0.1 mg/mL (insoluble)
Storage
4°C, away from moisture and light
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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