SCS-C003887

phyllactone E ?

Pathway: Terpenoids Superclass: Sesterterpenoids Class: Scalarane sesterterpenoids Glycoside

Chemical Structure

Structure of phyllactone E ?
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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

Carteriospongia foliascens (Sponge)
Nansha Islands
DOI: 10.1021/np50089a007  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
528.7 Da
Threshold ≤ 500
ALogP
5.86
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
6
Threshold ≤ 10
2 violations (MW, ALogP) — not drug-like by Ro5

Chemical Properties

Molecular Formula:
C32H48O6
Molecular Weight:
528.7300 Da
SMILES:
CCC(O)CC(=O)O[C@@H]1CC2[C@@]3(C)CCC[C@](C)(CC)C3CC[C@@]2(C)C2C=CC3=C(C(=O)O[C@]3(C)O)[C@]21C
InChIKey:
VFNCNKUOQSBSAZ-HAHNLAHRSA-N
InChI:
InChI=1S/C32H48O6/c1-8-19(33)17-25(34)37-24-18-23-29(4)15-10-14-28(3,9-2)21(29)13-16-30(23,5)22-12-11-20-26(31(22,24)6)27(35)38-32(20,7)36/h11-12,19,21-24,33,36H,8-10,13-18H2,1-7H3/t19?,21?,22?,23?,24-,28+,29+,30+,31-,32+/m1/s1
Calculated Properties
ALogP:
5.856 lipophilicity
TPSA:
93.06 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
6
Rotatable Bonds:
5
Ring Count:
5 (0 aromatic)
Chiral Centers:
10
Fsp³:
0.8125 fraction sp³ carbon

Database Information

Compound ID:
SCS-C003887
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Sesterterpenoids
NPClassifier Class:
Scalarane sesterterpenoids
Glycoside:
Yes
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged