SCS-C001518

(3R)-nordinone

Pathway: Polyketides Superclass: Macrolides Class: Zearalenones

Chemical Structure

Structure of (3R)-nordinone
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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
320.4 Da
Threshold ≤ 500
ALogP
3.50
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C18H24O5
Molecular Weight:
320.3850 Da
SMILES:
C[C@@H]1CCCCCCCC(=O)Cc2cc(O)cc(O)c2C(=O)O1
InChIKey:
JBVLZTRASUVBJM-GFCCVEGCSA-N
InChI:
InChI=1S/C18H24O5/c1-12-7-5-3-2-4-6-8-14(19)9-13-10-15(20)11-16(21)17(13)18(22)23-12/h10-12,20-21H,2-9H2,1H3/t12-/m1/s1
Calculated Properties
ALogP:
3.499 lipophilicity
TPSA:
83.83 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
5
Rotatable Bonds:
0
Ring Count:
2 (1 aromatic)
Chiral Centers:
1
Fsp³:
0.5556 fraction sp³ carbon

Database Information

Compound ID:
SCS-C001518
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 105.7 μM 10.3390/md15020035 Marine Drugs
Antitumor IC50 GH3 cell line 12.33 μM 10.3390/md15020035 Marine Drugs
Antitumor IC50 MMQ cell line 10.13 μM 10.3390/md15020035 Marine Drugs
Structure enlarged