Cladospirone bisepoxide

• CAT Number: M138377
• CAS Number: 152607-03-9
• Molecular Formula: C20H14O7
• Molecular Weight: 366.33
• Purity: ≥95%
• Target: Fungal
• Storage: Desiccate at -20C
• IUPAC Name: (1'S,2'S,3'R,5'R,7'R,11'S)-2',11'-dihydroxyspiro[2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene-3,6'-4,12-dioxatetracyclo[5.4.1.01,7.03,5]dodec-9-ene]-8'-one
• InChI: InChI=1S/C20H14O7/c21-12-7-8-13(22)19-18(12,27-19)16(23)15-17(24-15)20(19)25-10-5-1-3-9-4-2-6-11(26-20)14(9)10/h1-8,12,15-17,21,23H/t12-,15+,16-,17+,18-,19-/m0/s1
• InChIKey: AUWGMDYISSBOED-CCNMWVGKSA-N
• SMILES: C1=CC2=C3C(=C1)OC4([C@H]5[C@H](O5)[C@@H]([C@@]67[C@@]4(O6)C(=O)C=C[C@@H]7O)O)OC3=CC=C2

Cladospirone bisepoxide（Cat No.:M138377）is a synthetic compound derived from the natural product cladospirone, known for its potential pharmacological activity. It features a bisepoxide structure, which enhances its reactivity and interaction with biological targets. Cladospirone bisepoxide has been studied for its effects on neurotransmitter systems, particularly its impact on serotonin receptors, and has shown promise as a modulator of cognitive and mood-related processes. It may also have neuroprotective properties, offering potential applications in treating neurodegenerative diseases and psychiatric disorders. Its exact mechanism of action and therapeutic potential remain under active research.

Reference

1.PETERSEN, FRANK, et al. "Production of cladospirone bisepoxide, a new fungal metabolite." The Journal of antibiotics 47.10 (1994): 1098-1103.