Molecule

F1839-D

AlkaPlorer ID: AK044933

Synonym: None

IUPAC Name: (2R,3S,4aS,7R,8R,8aS)-2,3,4'-trihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-6,7-dihydro-3H-furo[3,2-g]isoindole]-8'-one

Structure

SMILES: C[C@@H]1CC[C@H]2C(C)(C)[C@H](O)[C@H](O)C[C@]2(C)[C@@]12CC1=C(O)C=C3CN=C(O)C3=C1O2

InChI: InChI=1S/C23H31NO5/c1-11-5-6-16-21(2,3)19(27)15(26)9-22(16,4)23(11)8-13-14(25)7-12-10-24-20(28)17(12)18(13)29-23/h7,11,15-16,19,25-27H,5-6,8-10H2,1-4H3,(H,24,28)/t11-,15-,16+,19-,22+,23-/m1/s1

InChIKey: NAYYHXFGJRKHMB-OKXHAOHDSA-N

Reference

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

PubChem CID: 10363682

LOTUS: LTS0175470

SuperNatural Ⅲ: SN0240598-02

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NPAtlas: NPA002529

Source

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

Properties Information

Molecule Weight: 401.50300000000016

TPSA？: 102.51

MolLogP？: 3.0882000000000014

Number of H-Donors: 4

Number of H-Acceptors: 5

RingCount: 5

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi