SCS-C005571

peaurantiogriseol D

Pathway: Polyketides Superclass: Cyclic polyketides Class: Monacolins and Monacolin derivatives

Chemical Structure

Structure of peaurantiogriseol 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

Penicillium aurantiogriseum (NA)
Qi'ao Mangrove Nature Reserve
DOI: 10.3390/md13106306  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
282.4 Da
Threshold ≤ 500
ALogP
1.43
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C16H26O4
Molecular Weight:
282.3800 Da
SMILES:
C[C@]1(O)CC[C@H]2[C@@H](C=C[C@@](C)(O)[C@]2(C)C(=O)CCO)C1
InChIKey:
LWCQKJINOCQTMW-AMSCCUFHSA-N
InChI:
InChI=1S/C16H26O4/c1-14(19)7-5-12-11(10-14)4-8-15(2,20)16(12,3)13(18)6-9-17/h4,8,11-12,17,19-20H,5-7,9-10H2,1-3H3/t11-,12-,14-,15+,16-/m0/s1
Calculated Properties
ALogP:
1.432 lipophilicity
TPSA:
77.76 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
4
Rotatable Bonds:
3
Ring Count:
2 (0 aromatic)
Chiral Centers:
5
Fsp³:
0.8125 fraction sp³ carbon

Database Information

Compound ID:
SCS-C005571
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Cyclic polyketides
NPClassifier Class:
Monacolins and Monacolin derivatives
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged