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Molecule
ID:5501
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₈H₂₂ClNOS
Molecular Mass
335.89138
Exact Mass
335.11106301
Charge
0
InChI
InChI=1S/C18H22ClNOS/c1-2-6-14-17(22-13-7-4-3-5-8-13)15-11-12(19)9-10-16(15)20-18(14)21/h9-11,13H,2-8H2,1H3,(H,20,21)
InChIKey
CLKFNGKDJYMUPK-UHFFFAOYSA-N
Canonic Smiles
CCCc1c(=O)[nH]c2c(c1SC1CCCCC1)cc(cc2)Cl
Isomeric Smiles
C1(CCCCC1)Sc1c(c(=O)[nH]c2c1cc(cc2)Cl)CCC
Calculated Properties
JChem
Acid pKa
13.215146
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
5.224566
LogD (pH = 7.4)
5.2245655
Log P
5.224566
Molar Refractivity
97.426
Polarizability
36.92952
Polar Surface Area
29.1
Rotatable Bonds
4
Lipinski's Rule of Five
false
ALOGPS 2.1
Log P
6.18
LOG S
-5.08
Solubility (Water)
2.81e-03 g/l
Data Source
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Properties
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Molecular Spectra
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Molecule Details
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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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ALOGPS 2.1
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Academic Data
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IUPAC Traditional name
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IUPAC name
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PubChem CID
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PubChem SID
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Related Proteins
Molecular Spectra
Molecule Details
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DrugBank
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
448727
DrugBank
DB07868
Names and Identifiers
Synonyms
6-CHLORO-4-(CYCLOHEXYLSULFANYL)-3-PROPYLQUINOLIN-2(1H)-ONE
IUPAC Traditional name
6-chloro-4-(cyclohexylsulfanyl)-3-propyl-1H-quinolin-2-one
IUPAC name
6-chloro-4-(cyclohexylsulfanyl)-3-propyl-1,2-dihydroquinolin-2-one
Registration numbers
PubChem CID
448727
PubChem SID
160968929
99444339
Molecule Details
DrugBank
DB07868
Drug information: experimental
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay