Chemical Structure : Ecubectedin
CAS No.: 2248127-53-7
Catalog No.: PC-27660Not For Human Use, Lab Use Only.
Ecubectedin is an ecteinascidin synthetic analogue and selective inhibitor of transcription, reducing cell proliferation and migration, as well as inducing S-phase cell cycle arrest and DNA damage in malignant pleural mesothelioma cells.
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Ecubectedin is an ecteinascidin synthetic analogue and selective inhibitor of transcription, reducing cell proliferation and migration, as well as inducing S-phase cell cycle arrest and DNA damage in malignant pleural mesothelioma cells.
Ecubectedin inhibits cell viability in a panel of twelve 2D-cultures of patient-derived MPM, independent of histotype or BAP1 status, with mean IC50 of 0.06 nM.
Ecubectedin strongly impairs invasion, migration and cell cycle of MPM cells, down-regulates DNA damage sensors (ABL1, BRCA1 and TP53) and up-regulated repair machinery genes (ATR, ATM, CHEK1, CHEK2, PRKDC and RAD51), activates the cGAS/STING pathway.
Ecubectedin induces immunogenic cell death and immune killing by CD8+T-lymphocytes, reshaping the MPM immune-environment.
Ecubectedin increased the efficacy of atezolizumab in immune-PDX models of MPM.
| M.Wt | 784.88 | |
| Formula | C41H44N4O10S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
CC1=CC2=C(C(O)=C1OC)[C@@H]3[C@H]4[C@H]5C6=C(OC(C)=O)C(C)=C7C(OCO7)=C6[C@H](COC([C@]8(C9=C(C%10=CC=CC=C%10N9)C[C@@H](CO)N8)CS5)=O)N4[C@@H](O)[C@@H](N3C)C2 |
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1. Salaroglio IC, et al. J Exp Clin Cancer Res. 2024 Dec 21;43(1):327.
2. Gorgels D, et al. Cancer Res Commun. 2026 Aug 14. doi: 10.1158/2767-9764.CRC-26-0377.

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