SCS-C001517

(E)-9-etheno-lasiodiplodin

Pathway: Polyketides Superclass: Macrolides Class: Zearalenones

Chemical Structure

Structure of (E)-9-etheno-lasiodiplodin
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3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Download: SDF SMILES

Source Information

Trichoderma sp. 307 (NA)
Kingdom Fungi Phylum Ascomycota Class Sordariomycetes Order Hypocreales Family Hypocreaceae Genus Trichoderma Species NA
Zhanjiang Mangrove National Nature Reserve
DOI: 10.3390/md15020035  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
290.4 Da
Threshold ≤ 500
ALogP
3.92
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C17H22O4
Molecular Weight:
290.4000 Da
SMILES:
COc1cc(O)cc2c1C(=O)OC(C)CCCCC/C=C/2
InChIKey:
YAWRBFVZUNLSKO-VQHVLOKHSA-N
InChI:
InChI=1S/C17H22O4/c1-12-8-6-4-3-5-7-9-13-10-14(18)11-15(20-2)16(13)17(19)21-12/h7,9-12,18H,3-6,8H2,1-2H3/b9-7+
Calculated Properties
ALogP:
3.923 lipophilicity
TPSA:
55.76 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
4
Rotatable Bonds:
1
Ring Count:
2 (1 aromatic)
Chiral Centers:
1
Fsp³:
0.4706 fraction sp³ carbon

Database Information

Compound ID:
SCS-C001517
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Macrolides
NPClassifier Class:
Zearalenones
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

Activity values are displayed only when a quantitative or clearly reported result is available. Tested organisms, cell lines and molecular targets are shown under Target / model.
Activity Assay Target / model Result Reference
Enzyme inhibition IC50 α-glucosidase 101.3 μM 10.3390/md15020035 Marine Drugs
Structure enlarged