SCS-C000036

fluostatin C

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Angucyclines

Chemical Structure

Structure of fluostatin C
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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
324.3 Da
Threshold ≤ 500
ALogP
1.70
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
6
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C18H12O6
Molecular Weight:
324.3000 Da
SMILES:
C[C@]12O[C@H]1[C@H](O)c1c(cc(O)c3c1C(=O)c1cccc(O)c1-3)C2=O
InChIKey:
CXDDSWUAYSPFRJ-BPQIPLTHSA-N
InChI:
InChI=1S/C18H12O6/c1-18-16(23)7-5-9(20)12-10-6(3-2-4-8(10)19)14(21)13(12)11(7)15(22)17(18)24-18/h2-5,15,17,19-20,22H,1H3/t15-,17+,18-/m1/s1
Calculated Properties
ALogP:
1.696 lipophilicity
TPSA:
107.36 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
6
Rotatable Bonds:
0
Ring Count:
5 (2 aromatic)
Chiral Centers:
3
Fsp³:
0.2222 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000036
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 > 64.0 μg/mL 10.1021/np300505y Journal of Natural Products
Antibacterial MIC S. aureus 16.0 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