Molecule

F1839-F

AlkaPlorer ID: AK027568

Synonym: None

IUPAC Name: methyl 4-[(2R,3S,4aS,7R,8R,8aS)-2,3,4'-trihydroxy-4,4,7,8a-tetramethyl-6'-oxospiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3,8-dihydrofuro[2,3-e]isoindole]-7'-yl]butanoate

Structure

SMILES: COC(=O)CCCN1CC2=C3O[C@]4(CC3=C(O)C=C2C1=O)[C@H](C)CC[C@H]1C(C)(C)[C@H](O)[C@H](O)C[C@@]14C

InChI: InChI=1S/C28H39NO7/c1-15-8-9-21-26(2,3)24(33)20(31)13-27(21,4)28(15)12-17-19(30)11-16-18(23(17)36-28)14-29(25(16)34)10-6-7-22(32)35-5/h11,15,20-21,24,30-31,33H,6-10,12-14H2,1-5H3/t15-,20-,21+,24-,27+,28-/m1/s1

InChIKey: OGPJWDUXARBBHQ-DHZUNVPCSA-N

Reference

Isolation, Characterization and Biological Activities of Novel Triprenyl Phenols as Pancreatic Cholesterol Esterase Inhibitors Produced by Stachybotrys sp. F-1839.

PubChem CID: 10413689

LOTUS: LTS0230636

SuperNatural Ⅲ: SN0264857-01

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NPAtlas: NPA001112

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Stachybotrys sp.	Stachybotrys	Stachybotryaceae	Hypocreales	Sordariomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 501.6200000000004

TPSA？: 116.53

MolLogP？: 3.179000000000002

Number of H-Donors: 3

Number of H-Acceptors: 7

RingCount: 5

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi