CAS 130395-54-9
:Spiro[2H-cyclohepta[b]furan-3(3aH),6'(2'H)-furo[2',3':5,6]cyclohepta[1,2-b]pyran]-2,2'-dione,7'-acetyl-3',3'a,4,4',4'a,7,8,8a,8'a,9',10',10'a-dodecahydro-8'a-hydroxy-7,9'-dimethyl-3'-methylene-6-[(1E)-3-oxo-1-butenyl]-,(3R,3aR,3'aR,4'aR,7R,8aS,8'aR,9'S,10
Description:
Spiro[2H-cyclohepta[b]furan-3(3aH),6'(2'H)-furo[2',3':5,6]cyclohepta[1,2-b]pyran]-2,2'-dione, 7'-acetyl-3',3'a,4,4',4'a,7,8,8a,8'a,9',10',10'a-dodecahydro-8'a-hydroxy-7,9'-dimethyl-3'-methylene-6-[(1E)-3-oxo-1-butenyl]-, (3R,3aR,3'aR,4'aR,7R,8aS,8'aR,9'S,10' is a complex organic compound characterized by its intricate polycyclic structure, which includes multiple fused rings and functional groups. The presence of spiro and furo moieties suggests unique stereochemical properties and potential biological activity. This compound features several chiral centers, indicating that it may exist in multiple stereoisomeric forms, which can significantly influence its chemical behavior and interactions. The acetyl and methylene groups contribute to its reactivity, while the hydroxyl group may enhance solubility and hydrogen bonding capabilities. Given its structural complexity, this substance may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry and natural product synthesis. Its CAS number, 130395-54-9, allows for precise identification in chemical databases.
Formula:C29H34O8
Synonyms:- Spiro[2H-cyclohepta[b]furan-3(3aH),6'(2'H)-furo[2',3':5,6]cyclohepta[1,2-b]pyran]-2,2'-dione,7'-acetyl-3',3'a,4,4',4'a,7,8,8a,8'a,9',10',10'a-dodecahydro-8'a-hydroxy-7,9'-dimethyl-3'-methylene-6-(3-oxo-1-butenyl)-,[3'aR-[3'aa,4'aa,6'b[3aR*,6(E),7R*,8aS*],8'ab,9'b,10'aa]]-
- Pungiolide A
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Found 4 products.
Pungiolide A
CAS:Pungiolide A exhibits moderate cytotoxicities with IC50 values in the range of 0.90-6.84 uM.Formula:C30H36O7Purity:98%Color and Shape:SolidMolecular weight:510.583Pungiolide A
CAS:<p>Pungiolide A is a fungal metabolite, which is derived from the endophytic fungus Seimatosporium. This compound exhibits a unique mode of action characterized by its potent cytotoxic activity. Pungiolide A interacts with cellular components, disrupting normal cellular functions, which results in the suppression of cell proliferation.</p>Formula:C30H36O7Purity:Min. 95%Molecular weight:508.60 g/mol




