ChemicalBook >> CAS DataBase List >>Verteporfin

Verteporfin

CAS No.
129497-78-5
Chemical Name:
Verteporfin
Synonyms
BPD-MA;Visudyne;CL 318952;NSC6242;NSC 6242;NSC-6242;VERTEPIRFIN;Verteprofin;Verteporfin;Verteporfen
CBNumber:
CB6505794
Molecular Formula:
2C41H42N4O8
Molecular Weight:
1437.61
MDL Number:
MFCD11982858
MOL File:
129497-78-5.mol
MSDS File:
SDS
Last updated:2026-03-09 18:40:30
Product description Number Pack Size Price
Verteporfin ≥94% (HPLC) SML0534 5mg $120
Verteporfin United States Pharmacopeia (USP) Reference Standard 1711461 200mg $1310
Verteporfin ≥95% 17334 1mg $32
Verteporfin ≥95% 17334 5mg $93
Verteporfin ≥94% (HPLC) SML0534 25mg $460.75
More product size

Verteporfin Properties

storage temp. -20°C
solubility DMSO: soluble2mg/mL, clear (warmed)
form powder
color Black
Stability Stable for 2 years from date of purchsae as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey YHNBVDZVUQFVLS-RDSGBMLISA-N
FDA UNII 0X9PA28K43
ATC code S01LA01
NCI Drug Dictionary verteporfin
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P280-P305+P351+P338
WGK Germany  3
HS Code  2933997500
Storage Class 11 - Combustible Solids

Verteporfin price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0534 Verteporfin ≥94% (HPLC) 129497-78-5 5mg $120 2025-07-31 Buy
Sigma-Aldrich 1711461 Verteporfin United States Pharmacopeia (USP) Reference Standard 129497-78-5 200mg $1310 2024-03-01 Buy
Cayman Chemical 17334 Verteporfin ≥95% 129497-78-5 1mg $32 2024-03-01 Buy
Cayman Chemical 17334 Verteporfin ≥95% 129497-78-5 5mg $93 2024-03-01 Buy
Sigma-Aldrich SML0534 Verteporfin ≥94% (HPLC) 129497-78-5 25mg $460.75 2025-07-31 Buy
Product number Packaging Price Buy
SML0534 5mg $120 Buy
1711461 200mg $1310 Buy
17334 1mg $32 Buy
17334 5mg $93 Buy
SML0534 25mg $460.75 Buy

Verteporfin Chemical Properties,Uses,Production

Photosensitizer

Verteporfin (trade name Visudyne) belongs to a second generation of porphyrin-based photosensitizer that can be activated by light (wavelength 689nm). It can be used for photodynamic therapy for macular degeneration. Drugs can selectively penetrate into the abnormal blood vessels, generate reactive oxygen species and occlude the abnormal blood vessels with the help of non-thermal laser irradiation, further terminating blood vessel leakage, and saving vision.
Upon being activated by the light, Visudyne forms a cytotoxic product in an aerobic environment. During this process, the porphyrin transfers the absorbed energy to oxygen and forms single-oxygen with a high activity and a short maintenance time. The single-oxygen destroys the biological structure within its range of diffusion. This process leads to localized vascular atresia and cell destruction, further leading to cell death in a particular environment.
In plasma, verteporfin is mainly carried by low density lipoprotein (LDL). The application of Visudyne for photodynamic therapy (PDT) has selectivity. On the one hand, it depends on the choice of light irradiation site. On the other hand, the expression of LDL receptors is enhanced in rapidly proliferating cells, including choroidal neovascular endothelial cells, so that rapid proliferative cells can selectively and rapidly ingest and accumulate verteporfin. Choroidal neovascularization is more rapid and selective than retinal pigment epithelium in absorbing the Visudyne, whereas in other ocular structures, the drug content is small. Therefore, the drug can selectively destroy choroidal neovascularization. It can be used for the treatment of continuous deterioration or loss of vision caused by wet age-related macular degeneration, pathological myopia and ocular histoplasmosis related to the choroidal neovascularization
The above information is edited Andy from ChemicalBook.

Administration and Dosage

Verteporfin is suitable for the treatment of patients of age-related macular degeneration, pathologic myopia or suspected ocular histoplasmosis with a typical predominantly central choroidal neovascularization. There is no sufficient evidence to support its efficacy on the treatment of patients with occult central choroidal neovascularization.
Intravenous administration, the drug treatment process contains two steps: ① intravenous administration: Formulate 2 mg/mL injection with sterile injection of water at a body surface area of 6 mg/m2. Diluted to 30 mL with 5% GS and inject for 10 minutes at the rate of 3mL/min. The diluent should be avoided of light within 4 hours. ② non-thermal diode laser activation: within the 15 minutes after the start of injection, apply a laser of constant energy at wavelength of 689 ± 3nm for irradiation towards patients. During the treatment of choroidal neovascularization, the recommended laser dose at the local focus should be 50 J/ cm2 with laser intensity of 600mW/cm2. The irradiation process should be completed within 83 seconds.

Adverse reactions

Common adverse effects of Visudyne include visual impairment. Local infusion and rash may occur during local injection. It can be occurred of cataract, diplopia, tears, conjunctivitis, dry eyes, eye itching, severe visual loss and conjunctiva, retinal and vitreous hemorrhage, high blood pressure, atrial fibrillation, peripheral vascular disorders, varicose veins, hypoesthesia, sleep disorders, headache, dizziness, weakness, fever, creatinine, cough, pharyngitis, pneumonia, influenza-like syndrome, back pain, abnormal liver function test indicators, prostate disorders, proteinuria, nausea, constipation, gastrointestinal cancer, eczema, anemia, reduction or increases in leukocyte count, hearing impairment and so on.

Precautions

Visudyne should be disabled in patients who are highly allergic to it and its derivatives, and patients who received other photosensitizers within 3 months or with porphyria. Patients of serious or moderately serious liver dysfunction should be cautious upon receiving vitamin treatment. Vitamin and other drugs should not be dissolved in the same solution. Avoid direct exposure to drugs. If a patient has a severe vision loss (vision loss or more than 4 lines) within 1 week after treatment, the patients should discontinue the treatment until the vision returns to the initial state. Care should be taken before weighing the pros and cons of treatment. Patients of liver dysfunction and photodynamic therapy discomfort should take with caution; patients, within 6 days after treatment, should avoid exposure of the skin and eyes to light; avoid excessive and prolonged treatment. Do not use in a brightly lit environment. Avoid the use of visudyne salt solution. If liquid spills, wipe it with a damp cloth. Do not let it touch the eye or skin. Verteporfin leakage may cause severe pain, inflammatory reactions, and discoloration at the injection site. Analgesics can be simultaneously given to relieve pain during the injection. If you find verteporfin leakage, immediately stop the injection, and give cold pressure. The affected area should be carefully protected against direct light exposure until swelling and skin color return to normal. Vitamins should be used with care for patients with general anesthesia.
Patients treated with Visudyne were in a light-sensitive state within 48 hours of injection. Within 48 hours of treatment, the skin and eyes mustn’t be exposed directly to daylight or bright artificial light. If you have to be exposed to the outdoors during the day within 48 hours of treatment, you should wear a suitable jacket and wear sunglasses for protection.

Description

Verteporfin was introduced in Switzerland as a second-generation photosensitizer for photodynamic therapy of wet age-related macular degeneration in patients with subfoveal choroidal neovascularisation. It is constituted of a mixture of two regioisomers resulting from nonselective monohydrolysis of the methyl tetraester. Upon irradiation with a lowenergy nonheat-generating laser light of 689nm wavelength, both regioisomeric benzoporphyrins are responsible for the local generation of singlet oxygen leading to free radical damage of neovascular endothelial cells in subfoveal lesions of patients with agerelated macular degeneration. The lipophilic drug is injected i.v. as a liposomal formulation in order to favor its uptake by plasma lipoproteins and distribution to cells with a high expression of low density lipoprotein receptors such as tumor and neovascular endothelial cells. Verteporfin is also being developed for the treatment of other eye diseases, nonmelanoma skin cancer and psoriasis.

Description

Verteporfin is a photosensitizer used during photodynamic therapy to eliminate abnormal blood vessels in the eye that are associated with conditions such as macular degeneration. It accumulates in these abnormal blood vessels and, when activated by nonthermal red light with a wavelength of 693 nm in the presence of oxygen, produces a highly reactive short-lived singlet oxygen and other reactive oxygen radicals, generating local damage to the endothelium and vessel occlusion. Verteporfin can also inhibit autophagosome formation by directly targeting and modifying p62, a scaffold and adaptor protein that binds both polyubiquitinated proteins destined for degradation and LC3 on autophagosomal membranes.

Originator

QLT Inc. (Canada)

Uses

Verteporfin is a photosensitizer that is used in photodynamic therapy (PDT). Verteporfin can accumulate in tumor tissues allowing for 30 to 150 minutes optimal PDT after intravenous administration.

Uses

Treatment of age-related macular degeneration

brand name

Visudyne (QLT).

Biochem/physiol Actions

Verteporfin is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as macular degeneration. Verteporfin accumulates in abnormal blood vessels and, when stimulated by nonthermal red light with a wavelength of 693 nm in the presence of oxygen, produces highly reactive short-lived singlet oxygen and other reactive oxygen radicals, resulting in local damage to the endothelium and blockage of the vessels. Verteporfin localizes predominantly in mitochondria.

storage

Store at -20°C

Background

Verteporfin is a benzoporphyrin derivative that is photoactivated by nonthermal red light in the presence of oxygen. It is used clinically as a photosensitizer in photodynamic therapy to treat selected vascular-related diseases. When photoactivated in vasculature, verteporfin generates reactive oxygen species that induce localized damage to endothelial cells, resulting in targeted vessel blockage. Established clinical uses of verteporfin include the treatment of age-related macular degeneration, subfoveal choroidal neovascularization, and pathological myopia; its anti-angiogenic effects have also led to its consideration as an anti-tumor agent. However, the cellular effects of verteporfin exposure extend beyond its photosensitizing activity. It has also been shown to block the interaction between the transcriptional co-activator YAP and TEAD family transcription factors, notably in the absence of photoactivation. This was shown to result in transcriptional repression of YAP target genes that regulate cell proliferation and cell death, suggesting an additional mechanism by which verteporfin could be utilized as an anti-tumor agent.

References

References/Citations:
(1)Saini et al. (2021), Verteporfin disrupts multiple steps of autophagy and regulates p53 to sensitize osteosarcoma cells; Cancer Cell Int., 21 52
(2)Vigneswaran et al. (2021), YAP/TAZ Transcription Coactivators Create Therapeutic Vulnerability to Verteporfin in EGFR-mutant Glioblastoma; Clin. Cancer Res., 27 1553
(3)Donohue et al. (2014), Induction of Covalently Crosslinked p62 Oligomers with Reduced Binding to Polyubiquitinated Proteins by the Autophagy Inhibitor Verteporfin; PLoS One, 9 e114964
(4)Luo et al. (2021), Src-Yap1 signaling axis controls the trophectoderm and epiblast lineage differentiation in mouse embryonic stem cells; Stem Cell Res., 54 102413
(5)Bressler et al. (2000), Photodynamic therapy with verteporfin (Visudyne): impact on ophthalmology and visual sciences; Invest. Ophthamol. Vis. Sci., 41 624

Verteporfin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 243)Suppliers
Supplier Tel Email Country ProdList Advantage
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533 Brad@rongnabiotech.com China 3375 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21595 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29830 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 965 58
Hangzhou Cyanochem Co., Ltd.
+86 17788583750 sales@cyanochem.com CHINA 281 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19552 58
TopScience Biochemical
00852-68527855 info@itopbiochem.com China Hong Kong 902 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569262 +86-15003564040 1061@dideu.com China 3982 58

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View Lastest Price from Verteporfin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Verteporfin pictures 2026-03-09 Verteporfin
129497-78-5
US $1.00 / g 1g 0.99 20 tons RongNa Biotechnology Co.,Ltd
Verteporfin pictures 2026-03-09 Verteporfin
129497-78-5
US $34.00-77.00 / mg 98.94% 10g TargetMol Chemicals Inc.
Verteporfin pictures 2019-07-06 Verteporfin
129497-78-5
US $1.00 / KG 1KG 99% 200kg Career Henan Chemical Co
  • Verteporfin pictures
  • Verteporfin
    129497-78-5
  • US $1.00 / g
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Verteporfin pictures
  • Verteporfin
    129497-78-5
  • US $34.00-77.00 / mg
  • 98.94%
  • TargetMol Chemicals Inc.
  • Verteporfin pictures
  • Verteporfin
    129497-78-5
  • US $1.00 / KG
  • 99%
  • Career Henan Chemical Co

Verteporfin Spectrum

Verteporfin(DB00460) Verteprofin Visudyne Verteporfin Verteporphin 24H,26H-Benzo[b]porphine-9,13-dipropanoic acid, 18-ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-, monomethyl ester, (4R,4aS)-rel- VERTEPIRFIN 9-methyl (I)13-methyl (II)trans-(±)- 18-ethenyl- 4,4a-dihydro-3,4 -bis(methoxycarbonyl)- 4a,8,14,19-tetramethyl- 23H,25H-benzo[b]porphine- 9,13- dipropanoate (4R,4aS)-rel-18-ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-24H,26H-Benzo[b]porphine-9,13-dipropanoic acid monomethyl ester CL 318952 3-[(23S,24R)-14-Ethenyl-5-(3-methoxy-3-oxopropyl)-22,23-bis(methoxycarbonyl)-4,10,15,24-tetramethyl-25,26,27,28-tetraazahexacyclo[16.6.1.13,6.18,11.113,16.019,24]octacosa-1,3,5,7,9,11(27),12,14,16,18(25),19,21-dodecaen-9-yl]propanoic acid (4R,4aS)-18-Ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-24H,26H-benzo[b]porphine-9,13-dipropanoic acid monomethyl ester Verteporfin (Visudyne) VERTEPORFIN (200 MG) trans-3,4-Dicarboxy-4,4a-dihydro-4a,8,14,19-tetramethyl-18-vinyl-23H,25H-benzo(b)porphine-9,13-dipropionic acid 3,4,9-trimethyl ester BPD-MA Verteporfin USP/EP/BP Verteporfin (DB-00460, CL-318952, BPD-MA, BpdMA) VerteporfinQ: What is Verteporfin Q: What is the CAS Number of Verteporfin Q: What is the storage condition of Verteporfin Q: What are the applications of Verteporfin Verteporfen Verteporfin (1711461) N-Diethylformamide NSC 6242 NSC6242 NSC-6242 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 18-ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-, monomethyl ester, trans- Verteporfin,inhibit,CL318952,CL-318952,Yes-associated protein,Autophagy,Apoptosis,Inhibitor,YAP Verteporfin (CL 318952) Verteporfin (Visudyne), Benzoporphyrin derivative Verteporfin, 10 mM in DMSO Verteporfin - mixture of isomer 129497-78-5 C41H42N4O8 2C41H42N4O8 Visudyne Inhibitors APIs