monoaspartyl chlorin e6
- Product Name
- monoaspartyl chlorin e6
- CAS No.
- 110230-98-3
- Chemical Name
- monoaspartyl chlorin e6
- Synonyms
- Talaporfin;Talaporfin free acid;monoaspartyl chlorin e6;VSEIDZLLWQQJGK-BRXYURPTSA-N;monoaspartyl chlorin e6 or 220201-34-3((sodium salt);N-[2-[(7S,8S)-3-Carboxy-7-(2-carboxyethyl)-13-ethenyl-18-ethyl-7,8-dihydro-2,8,12,17-tetramethyl-21H,23H-porphin-5-yl]acetyl]-L-aspartic acid;L-Aspartic acid, N-[2-[(7S,8S)-3-carboxy-7-(2-carboxyethyl)-13-ethenyl-18-ethyl-7,8-dihydro-2,8,12,17-tetramethyl-21H,23H-porphin-5-yl]acetyl]-;(2S)-2-[[2-[(2S,3S)-7-carboxy-3-(2-carboxyethyl)-17-ethenyl-12-ethyl-2,8,13,18-tetramethyl-2,3,23,24-tetrahydroporphyrin-5-yl]acetyl]amino]butanedioic acid
- CBNumber
- CB71349435
- Molecular Formula
- C38H41N5O9
- Formula Weight
- 711.76
- MOL File
- 110230-98-3.mol
monoaspartyl chlorin e6 Property
- Boiling point:
- 1218.1±65.0 °C(Predicted)
- Density
- 1.359
- storage temp.
- -20°C Freezer
- solubility
- DCM, EA, MeOH
- form
- Solid
- color
- Dark
monoaspartyl chlorin e6 Chemical Properties,Usage,Production
Description
In collaboration with Light Sciences Corp. and Meiji Seika Kaisha, Nippon Petrochemicals has developed and launched the injectable photosensitizer talaporfin sodium in Japan for the photodynamic therapy (PDT) of cancer. The initial approval is for the treatment of early stage lung cancer, but Light Sciences Corp. and its subsidiaries are also developing talaporfin sodium for other hyperproliferative diseases, such as, liver metastases arising from colorectal cancer, wet age-related macular degeneration, and atherosclerosis. Talaporfin sodium is typically supplied as a lyophilized green powder, and it is synthesized via a carbodiimide-mediated coupling of chlorin e6 (obtained from precursors that were extracted from natural sources) with L-aspartic acid. Since chlorin e6 contains three carboxylic acid groups, the coupling reaction produces a mixture of aspartic acid conjugates. The desired site of conjugation is the acetic acid side chain of C-20, and the other regioisomers are removed by chromatographic purification. Compared to other photosensitizers, talaporfin sodium is associated with minimal cutaneous photosensitivity, is activated at long wavelengths permitting deeper tissue penetration, and requires a shorter interval between intravenous administration and photoactivation. It has a serum half-life of nine hours and is excreted unmetabolized, predominantly by the biliary system. In the clinical study of patients with early lung cancer, a complete response was obtained in approximately 86% of the lesions (administration at 40 mg/m2 followed by laser irradiation at 100 J/cm2, 4–6 hours later). In addition to laser activation, a clinical study involving a variety of refractory solid tumors demonstrated that intratumoral delivery of light-emitting diodes was effective; a 33% overall response rate was observed with no cutaneous phototoxicity. Regardless of the mode of activation, the outcome is the same; the activated photosensitizer reacts with endogenous oxygen to generate singlet oxygen that ultimately leads to apoptosis and vascular ischemia of the targeted tissue. The most significant adverse effect associated with talaporfin sodium was generalized cutaneous photosensitivity, and erythema and oedema were common as well. Individual cases of nausea, vomiting, diarrhea, heartburn, headache, and pruritus were also reported.
Originator
Nippon Petrochem. (Japan)
Uses
Talaporfin is a photosensitizer used in photodynamic therapy.
Definition
ChEBI: Talaporfin is a member of chlorins.
brand name
Laserphyrin
monoaspartyl chlorin e6 Preparation Products And Raw materials
Raw materials
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