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Molecule
ID:120188
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₁NO₄
Molecular Mass
245.23074
Exact Mass
245.06880784
Charge
0
InChI
InChI=1S/C13H11NO4/c1-16-8-2-3-11-9(6-8)12-10(7-14-11)13(15)18-5-4-17-12/h2-3,6-7H,4-5H2,1H3
InChIKey
MRUROZNFQGNOFD-UHFFFAOYSA-N
Canonic Smiles
COc1ccc2c(c1)c1OCCOC(=O)c1cn2
Isomeric Smiles
c12c(c3c(nc2)ccc(c3)OC)OCCOC1=O
Calculated Properties
JChem
H Acceptors
4
H Donor
0
LogD (pH = 5.5)
1.4170672
LogD (pH = 7.4)
1.4471117
Log P
1.44751
Molar Refractivity
62.962
Polarizability
25.675447
Polar Surface Area
57.65
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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PubChem CID
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PubChem SID
Properties
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_NC-2734
STOCK1N-76790
Academic Data
PubChem
50877399
Names and Identifiers
IUPAC Traditional name
10-methoxy-2H,3H-[1,4]dioxepino[6,5-c]quinolin-5-one
IUPAC name
10-methoxy-2H,3H,5H-[1,4]dioxepino[6,5-c]quinolin-5-one
Synonyms
10-methoxy-2H-[1,4]dioxepino[6,5-c]quinolin-5(3H)-one
Registration numbers
PubChem CID
50877399
PubChem SID
162214541
Properties
Product Information
Classification
Derivatives & analogs of Natural Compounds
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay