SCS-C007291

methyl 6-acetyl-4-methoxy-5,8-dihydroxynaphthalene-2-carboxylate

Pathway: Polyketides Superclass: Naphthalenes Class: Naphthalenes and derivatives

Chemical Structure

Structure of methyl 6-acetyl-4-methoxy-5,8-dihydroxynaphthalene-2-carboxylate
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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

Aspergillus terreus (mangrove endophytic fungus)
Kingdom Fungi Phylum Ascomycota Class Eurotiomycetes Order Eurotiales Family Aspergillaceae Genus Aspergillus Species Aspergillus terreus
South China Sea
DOI: 10.1016/s1875-5364(19)30017-2  · Chinese Journal of Natural Medicines

Drug-likeness (Lipinski Ro5)

Molecular Weight
290.3 Da
Threshold ≤ 500
ALogP
2.25
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
6
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H14O6
Molecular Weight:
290.2710 Da
SMILES:
COC(=O)c1cc(OC)c2c(O)c(C(C)=O)cc(O)c2c1
InChIKey:
XBVGVYLRFOYWSF-UHFFFAOYSA-N
InChI:
InChI=1S/C15H14O6/c1-7(16)9-6-11(17)10-4-8(15(19)21-3)5-12(20-2)13(10)14(9)18/h4-6,17-18H,1-3H3
Calculated Properties
ALogP:
2.249 lipophilicity
TPSA:
93.06 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
6
Rotatable Bonds:
3
Ring Count:
2 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.2000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007291
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Naphthalenes
NPClassifier Class:
Naphthalenes and derivatives
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
Antimycobacterial inhibition rate Mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB) < 60.0 % 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Antitumor activity level human glioma U87 cells all these compounds (1?17) exhibited weak or no cytotoxic activities towards human glioma U87 cells at a concentration of 10 μmol·L?1 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Neuroprotective / Neuromodulatory activity level glutamate-induced toxicity in HT22 cells — Structured numeric value is not available in this record; see the primary reference. 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Structure enlarged