SCS-C000638

cladosin C

Pathway: Alkaloids Superclass: Tetramate alkaloids Class: Simple tetramate alkaloids

Chemical Structure

Structure of cladosin 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

Cladosporium sphaerospermum (NA)
South China Sea  · #NAME?
DOI: 10.1021/np400833x  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
250.3 Da
Threshold ≤ 500
ALogP
1.57
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C13H18N2O3
Molecular Weight:
250.2900 Da
SMILES:
CC(C)=C1NC(=O)C(C(=N)/C=C/C[C@H](C)O)=C1O
InChIKey:
NRYAZWLSPQPXOQ-KWXKUKOQSA-N
InChI:
InChI=1S/C13H18N2O3/c1-7(2)11-12(17)10(13(18)15-11)9(14)6-4-5-8(3)16/h4,6,8,14,16-17H,5H2,1-3H3,(H,15,18)/b6-4+,14-9?/t8-/m0/s1
Calculated Properties
ALogP:
1.569 lipophilicity
TPSA:
93.41 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
4
Rotatable Bonds:
4
Ring Count:
1 (0 aromatic)
Chiral Centers:
1
Fsp³:
0.3846 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000638
NPClassifier Pathway:
Alkaloids
NPClassifier Superclass:
Tetramate alkaloids
NPClassifier Class:
Simple tetramate alkaloids
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
Antiviral IC50 influenza A H1N1 virus IC50=~μM 10.1021/np400833x Journal of Natural Products
Structure enlarged