SCS-C000037

fluostatin D

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Angucyclines

Chemical Structure

Structure of fluostatin D
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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
394.4 Da
Threshold ≤ 500
ALogP
2.90
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
7
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C22H18O7
Molecular Weight:
394.4000 Da
SMILES:
CC(C)C(=O)O[C@@H]1c2c(cc(O)c3c2C(=O)c2cccc(O)c2-3)C(=O)[C@@]2(C)O[C@@H]12
InChIKey:
UIKYAUSFWRLFDK-KAGYGMCKSA-N
InChI:
InChI=1S/C22H18O7/c1-8(2)21(27)28-18-14-10(19(26)22(3)20(18)29-22)7-12(24)15-13-9(17(25)16(14)15)5-4-6-11(13)23/h4-8,18,20,23-24H,1-3H3/t18-,20+,22-/m1/s1
Calculated Properties
ALogP:
2.903 lipophilicity
TPSA:
113.43 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
7
Rotatable Bonds:
2
Ring Count:
5 (2 aromatic)
Chiral Centers:
3
Fsp³:
0.3182 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000037
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