| Size | Price | Stock |
|---|---|---|
| 100mg | $36 | In-stock |
| 200 mg | Get quote | |
| 500 mg | Get quote | |
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| Cat. No. : | HY-B1247 |
| M.Wt: | 562.66 |
| Formula: | C34H34N4O4 |
| Purity: | >98 % |
| Solubility: | DMSO : 2 mg/mL (ultrasonic;warming;heat to 60°C);Ethanol : < 1 mg/mL (ultrasonic) |
Protoporphyrin IX is a final intermediate in the heme biosynthetic pathway, which acts as a radiation sensitizer enhancing ROS generation even in a hypoxic state and inducing DNA damage. Protoporphyrin IX also acts as a photo sensitizer undergoing photobleaching that occurs through direct degradation by light irradiation. Protoporphyrin IX is formed and accumulated following 5-aminolevulinic acid (5-ALA) (HY-W000450) administration in the tumor cells of rats. Protoporphyrin IX causes selective improvement of basal cell carcinoma when activated red fluorescence of a peak wavelength at 405 nm. Protoporphyrin IX is promising for research of sonodynamic and photodynamic agents for a wide range of cancers, such as bladder cancer and nodular basal cell carcinoma[1][2][3][4][5].
In Vitro: Aminolevulinic acid (HY-W000450) (40 mg/kg, p.o., a single dose) produces full-thickness Protoporphyrin IX fluorescence in the five superficial, nodular and morpheaform basal cell carcinoma[3].
Protoporphyrin IX (3.6 nmol/g tissue) tissue can cause necrosis in normal rat colonic mucosa on exposure to light[4].
Protoporphyrin IX (6.6 nmol/g tumor) delays tumor growth after irradiation of a tumor in rats[4].
Protoporphyrin IX (0-25 μM, 2 h) rapidly results in increased nuclear G4 levels in Hela cells[5].
In Vivo: The highest level of Protoporphyrin IX (approximately 6.3 nmol/g tissue) is found in rat liver and intestine, followed by aorta (4.3 nmol/g tissue) and oesophagus (2.1 nmol/g tissue), 3 h after Aminolevulinic acid (300 mg/kg, i.v., a single dose) administration[4].
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