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Molecule
ID:124692
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₆N₂O
Molecular Mass
122.12464
Exact Mass
122.04801282
Charge
0
InChI
InChI=1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)
InChIKey
IBBMAWULFFBRKK-UHFFFAOYSA-N
Canonic Smiles
NC(=O)c1ccccn1
Isomeric Smiles
C(=O)(c1ncccc1)N
Calculated Properties
JChem
LogD (pH = 7.4)
-0.01
LogD (pH = 5.5)
-0.01
Log P
-0.01
Rotatable Bonds
1
H Donor
1
H Acceptors
2
Lipinski's Rule of Five
true
Acid pKa
2.17
Polar Surface Area
55.98
Polarizability
11.80
Molar Refractivity
32.61
LOG S
-0.61
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
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
•
Sigma Aldrich
•
TRC
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_SC-9415
Sigma Aldrich
104051
TRC
P437000
Alfa Aesar
A15410
Academic Data
PubChem
15070
ChEBI
CHEBI:8200
Names and Identifiers
Synonyms
picolinamide
2-吡啶甲酰胺
2-Pyridinecarboxamide
Picolinamide
吡啶酰胺
NSC 524473
Picolinic Acid Amide
α-Picolinamide
Picolinamide
2-Carbamoylpyridine
Picolinoylamide
α-Picolinic Acid Amide
吡啶-2-甲酰胺
Pyridine-2-carboxamide
α-(Aminocarbonyl)pyridine
α-Pyridinecarboxamide
2-carbamoylpyridine
Picolinamide
2-pyridinecarboxamide
picolinic acid amide
picolinoylamide
2-aminocarbonyl-pyridine
alpha-picolinamide
IUPAC Traditional name
pyridine-2-carboxamide
IUPAC name
pyridine-2-carboxamide
Registration numbers
CAS Number
1452-77-3
MDL Number
MFCD00023483
PubChem SID
24846635
162219045
8147004
EC Number
215-921-5
PubChem CID
15070
Beilstein Number
109617
Patent number
WO2006091963
WO2005051914
GB2225574
WO2005035507
WO2005061465
WO2005069981
US2007185152
WO2005039506
WO2006002383
WO2005110992
US2008293696
WO2005047294
WO2006095159
WO2005085227
WO2005115986
WO2005021553
EP1134214
BKMS React Database
154959
51521
42228
BRENDA Ligand Database
154959
42228
51521
MetaboLights Database
MTBLS2878
MTBLS1622
MTBLS1693
MTBLS630
MTBLS751
MTBLS360
MTBLS2559
MTBLS379
MTBLS570
CompTox Database
DTXSID4061703
Reaxys Registry
109617
SureChEMBL Database
SCHEMBL61183
CHEBI ID
CHEBI:8200
BRENDA Database
2.4.2.30
3.5.1.4
4.2.1.84
KEGG ID
C01950
ACToR Database
1452-77-3
NMRShiftDB Database
20200308
Protein Data Bank
4n1p
Gmelin ID
406092
PubMed Citation Links
23465187
Related Proteins
PDB Bank
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4N1P
Molecule Details
Sigma Aldrich
104051
Packaging
10, 50 g in glass bottle
TRC
P437000
A nicotinic acid derivative for prevention and treatment of cancer by activating RUNX3 gene.
ChEBI
CHEBI:8200
A pyridinecarboxamide that is the monocarboxylic acid amide derivative of picolinic acid.
References
PubChem Literature
From Data Sources
•
Cai., et al.: J. Med. Chem., 46, 2474 (1990)
•
Gupta., et al.: Biomed. Environ. Sci., 13,122 (1990)
•
Ludwig, et al.: Cancer Res., 50, 2470 (1990)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
EC Number
•
PubChem CID
•
Beilstein Number
•
Patent number
•
BKMS React Database
•
BRENDA Ligand Database
•
MetaboLights Database
•
CompTox Database
•
Reaxys Registry
•
SureChEMBL Database
•
CHEBI ID
•
BRENDA Database
•
KEGG ID
•
ACToR Database
•
NMRShiftDB Database
•
Protein Data Bank
•
Gmelin ID
•
PubMed Citation Links
Properties
Safety Information
Risk Statements
36/37/38
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
26
-
37/39
Source
26
-
37
Source
3
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
Warning
Source
Download link
Source
Download link
Source
是
Source
Product Information
98%
Source
C6H6N2O
Source
Download link
Source
Physical Property
110 °C (dec.)(lit.)
Source
104-108°C
Source
143°C/20mm
Source
Source
GHS Pictograms
GHS Precautionary statements
Safety Statements
German water hazard class
Personal Protective Equipment
GHS Signal Word
MSDS Link
TSCA Listed
Purity
Empirical Formula (Hill Notation)
Certificate of Analysis
Melting Point
Boiling Point