SCS-C000041

phenanthroviridone

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Angucyclines

Chemical Structure

Structure of phenanthroviridone
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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

Micromonospora rosaria (NA)
South China Sea  · -30m  · E 116°17.754', N 22°41.083'
DOI: 10.1021/np300505y  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
305.3 Da
Threshold ≤ 500
ALogP
2.73
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:
C18H11NO4
Molecular Weight:
305.3000 Da
SMILES:
Cc1cc(O)c2c3c(ncc2c1)C(=O)c1c(O)cccc1C3=O
InChIKey:
YUPGXNABNFYQMU-UHFFFAOYSA-N
InChI:
InChI=1S/C18H11NO4/c1-8-5-9-7-19-16-15(13(9)12(21)6-8)17(22)10-3-2-4-11(20)14(10)18(16)23/h2-7,20-21H,1H3
Calculated Properties
ALogP:
2.730 lipophilicity
TPSA:
87.49 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
5
Rotatable Bonds:
0
Ring Count:
4 (3 aromatic)
Chiral Centers:
0
Fsp³:
0.0556 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000041
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Polycyclic aromatic polyketides
NPClassifier Class:
Angucyclines
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
Antibacterial MIC Escherichia coli ATCC 25922 32.0 μg/mL 10.1021/np300505y Journal of Natural Products
Antibacterial MIC Staphylococcus aureus ATCC 29213 0.25 μg/mL 10.1021/np300505y Journal of Natural Products
Antibacterial MIC Bacillus thuringiensis SCSIO BT01 4.0 μg/mL 10.1021/np300505y Journal of Natural Products
Antibacterial MIC Bacillus subtilis SCSIO BS01 64.0 μg/mL 10.1021/np300505y Journal of Natural Products
Antitumor IC50 SF-268 0.09 ± 0.04 μM 10.1021/np300505y Journal of Natural Products
Antitumor IC50 MCF-7 0.17 ± 0.02 μM 10.1021/np300505y Journal of Natural Products
Antitumor IC50 NCI-H460 2.18 ± 0.01 μM 10.1021/np300505y Journal of Natural Products
Structure enlarged