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Molecule
ID:123799
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₀N₄OS
Molecular Mass
234.2776
Exact Mass
234.05753196
Charge
0
InChI
InChI=1S/C10H10N4OS/c1-6-13-14-10(16-6)12-9(15)7-3-2-4-8(11)5-7/h2-5H,11H2,1H3,(H,12,14,15)
InChIKey
KFASJMUGPCYEKL-UHFFFAOYSA-N
Canonic Smiles
Nc1cccc(c1)C(=O)Nc1nnc(s1)C
Isomeric Smiles
c1(sc(nn1)C)NC(=O)c1cc(N)ccc1
Calculated Properties
JChem
Acid pKa
7.9895315
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.81639683
LogD (pH = 7.4)
0.7246406
Log P
0.8185655
Molar Refractivity
65.5371
Polarizability
22.817778
Polar Surface Area
80.9
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
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Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
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PubChem CID
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PubChem SID
Properties
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
45493978
Commercial Catalog
InterBioScreen
BB_SC-7933
Names and Identifiers
IUPAC Traditional name
3-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide
IUPAC name
3-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide
Synonyms
3-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide
Registration numbers
PubChem CID
45493978
PubChem SID
162218152
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay