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| Chemical distributor since 2001 | ||||
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| Classification | API >> Antibiotics |
|---|---|
| Name | Trabectedin |
| Synonyms | Ecteinascidin; Ecteinascidin 743; Ecteinascidine 743; Et 743; NSC 648766 |
| Molecular Structure | ![]() |
| Molecular Formula | C39H43N3O11S |
| Molecular Weight | 761.84 |
| CAS Registry Number | 114899-77-3 |
| EC Number | 695-026-8 |
| SMILES | CC1=CC2=C([C@@H]3[C@@H]4[C@H]5C6=C(C(=C7C(=C6[C@@H](N4[C@H]([C@H](C2)N3C)O)COC(=O)[C@@]8(CS5)C9=CC(=C(C=C9CCN8)O)OC)OCO7)C)OC(=O)C)C(=C1OC)O |
| Solubility | Practically insoluble (0.055 g/L) (25 ºC), Calc.* |
|---|---|
| Density | 1.55±0.1 g/cm3 (20 ºC 760 Torr), Calc.* |
| * | Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2013 ACD/Labs) |
| Hazard Symbols |
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| Hazard Statements | H300-H312-H332-H341-H361-H373 Details | ||||||||||||||||||||||||||||||||
| Precautionary Statements | P203-P260-P261-P264-P270-P271-P280-P301+P316-P302+P352-P304+P340-P317-P318-P319-P321-P330-P362+P364-P405-P501 Details | ||||||||||||||||||||||||||||||||
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| SDS | Available | ||||||||||||||||||||||||||||||||
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Trabectedin, originally designated ET-743, was isolated from the Caribbean tunicate Ecteinascidia turbinata in the late 1980s. Its discovery resulted from bioprospecting efforts to find novel marine-derived compounds with anticancer properties. Trabectedin stood out for its unique mechanism of action, distinct from traditional cytotoxic agents, targeting DNA repair mechanisms and transcription regulation. Trabectedin has demonstrated efficacy in the treatment of advanced soft tissue sarcomas, including liposarcoma and leiomyosarcoma, as well as ovarian cancer, particularly in patients with platinum-sensitive disease. Its ability to inhibit transcription factors, such as FUS-CHOP in myxoid liposarcoma, makes it particularly effective against certain subtypes of sarcomas. Trabectedin has also shown activity against recurrent ovarian cancer when used in combination with pegylated liposomal doxorubicin. Additionally, trabectedin exhibits immunomodulatory effects, enhancing the antitumor activity of immune cells within the tumor microenvironment. Despite its efficacy, trabectedin is associated with notable side effects, including myelosuppression and hepatotoxicity, requiring careful patient monitoring. Ongoing research aims to elucidate its role in combination therapies and explore its potential in other cancer types, highlighting trabectedin as a valuable option for patients with challenging-to-treat malignancies. |
| Market Analysis Reports |
| List of Reports Available for Trabectedin |