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Molecule
ID:115128
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₀N₄O
Molecular Mass
226.234
Exact Mass
226.08546096
Charge
0
InChI
InChI=1S/C12H10N4O/c1-8-4-2-3-5-10(8)16-11-9(6-15-16)12(17)14-7-13-11/h2-7H,1H3,(H,13,14,17)
InChIKey
HJCRMBPAGYFMQE-UHFFFAOYSA-N
Canonic Smiles
Cc1ccccc1n1ncc2c1nc[nH]c2=O
Isomeric Smiles
c12n(ncc1c(=O)[nH]cn2)c1c(C)cccc1
Calculated Properties
JChem
Acid pKa
9.516694
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
1.4132355
LogD (pH = 7.4)
1.4103441
Log P
1.4132727
Molar Refractivity
65.5556
Polarizability
23.831007
Polar Surface Area
59.28
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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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
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RDKit
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IUPAC name
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IUPAC Traditional name
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MDL Number
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PubChem CID
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PubChem SID
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Product Information
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Physical Property
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
Academic Data
PubChem
16462965
Commercial Catalog
Life Chemicals
F2135-0121
Enamine
EN300-78518
Names and Identifiers
Synonyms
1-(2-methylphenyl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one
IUPAC name
1-(2-methylphenyl)-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one
IUPAC Traditional name
1-(2-methylphenyl)-5H-pyrazolo[3,4-d]pyrimidin-4-one
Registration numbers
MDL Number
MFCD11205130
MFCD09250835
PubChem CID
16462965
PubChem SID
162099867
Properties
Product Information
Purity
95+%
Source
95%
Source
Physical Property
Partition Coefficient
1.02653
Source
Hydrophobicity(logP)
1.76
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay