SCS-C000035

fluostatin K

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Angucyclines

Chemical Structure

Structure of fluostatin K
Loading 3D structure...
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
308.3 Da
Threshold ≤ 500
ALogP
2.27
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:
C18H12O5
Molecular Weight:
308.3000 Da
SMILES:
C[C@]1(O)C=Cc2c(cc(O)c3c2C(=O)c2cccc(O)c2-3)C1=O
InChIKey:
CKTLJJYDUPSLCZ-SFHVURJKSA-N
InChI:
InChI=1S/C18H12O5/c1-18(23)6-5-8-10(17(18)22)7-12(20)15-13-9(16(21)14(8)15)3-2-4-11(13)19/h2-7,19-20,23H,1H3/t18-/m0/s1
Calculated Properties
ALogP:
2.270 lipophilicity
TPSA:
94.83 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
5
Rotatable Bonds:
0
Ring Count:
4 (2 aromatic)
Chiral Centers:
1
Fsp³:
0.1111 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000035
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 E. coli, B. thuringiensis, B. subtilis, S. aureus > 64.0 μg/mL 10.1021/np300505y Journal of Natural Products
Antitumor IC50 SF-268, MCF-7, NCI-H460 > 100.0 μM 10.1021/np300505y Journal of Natural Products
Structure enlarged