SCS-C008245

lupinacidin A

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Anthraquinones and anthrones

Chemical Structure

Structure of lupinacidin A
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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 sp. SCSIO 07396 (NA)
Kingdom Bacillati Phylum Actinomycetota Class Actinomycetes Order Micromonosporales Family Micromonosporaceae Genus Micromonospora Species NA
South China Sea
DOI: 10.1021/acs.jnatprod.6c00037  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
340.4 Da
Threshold ≤ 500
ALogP
3.48
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C20H20O5
Molecular Weight:
340.3750 Da
SMILES:
Cc1c(O)c(CCC(C)C)c2c(c1O)C(=O)c1cccc(O)c1C2=O
InChIKey:
WWUQQOQPOGZVSK-UHFFFAOYSA-N
InChI:
InChI=1S/C20H20O5/c1-9(2)7-8-12-15-16(18(23)10(3)17(12)22)19(24)11-5-4-6-13(21)14(11)20(15)25/h4-6,9,21-23H,7-8H2,1-3H3
Calculated Properties
ALogP:
3.476 lipophilicity
TPSA:
94.83 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
5
Rotatable Bonds:
3
Ring Count:
3 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.3000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C008245
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Polycyclic aromatic polyketides
NPClassifier Class:
Anthraquinones and anthrones
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
Antitumor — PANC-1, TE-1, HL60, A549, MDA-MB-231, and GSC0722 the cytotoxicity of 1–10 was evaluated against six human tumor cell lines (PANC-1, TE-1, HL60, A549, MDA-MB-231, and GSC0722); only 8 was cytotoxic against the GSC0722 cancer cell line 10.1021/acs.jnatprod.6c00037 Journal of Natural Products
Structure enlarged