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Molecule
ID:69354
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₅NO₄
Molecular Mass
167.1189
Exact Mass
167.02185765
Charge
0
InChI
InChI=1S/C7H5NO4/c9-6(10)4-1-2-5(7(11)12)8-3-4/h1-3H,(H,9,10)(H,11,12)
InChIKey
LVPMIMZXDYBCDF-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1ccc(cn1)C(=O)O
Isomeric Smiles
c1(ccc(cn1)C(=O)O)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-6.05
LogD (pH = 5.5)
-4.22
Log P
-1.24
Rotatable Bonds
2
H Donor
2
H Acceptors
5
Lipinski's Rule of Five
true
Acid pKa
0.79
Polar Surface Area
87.49
Polarizability
14.58
Molar Refractivity
38.04
LOG S
-0.67
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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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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TRC
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ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02151986
05201412
InterBioScreen
BB_SC-7174
Matrix Scientific
074829
Sigma Aldrich
P63603
82787
TRC
P991640
Chemik
CHH00118
Bide Pharmatech
BD17209
Academic Data
PubChem
7493
ChEBI
CHEBI:46865
Names and Identifiers
Synonyms
2,5-Pyridinedicarboxylic acid
ISOCINCHOMERONIC ACID
pyridine-2,5-dicarboxylic acid
Isocinchomeronic acid
吡啶-2,5-二羧酸
2,5-Pyridinedicarboxylic acid
2,5-吡啶二羧酸
2,5-Dicarboxypyridine
NSC 177
Isocinchomeronic acid
pyridinedicarboxylic acid-(2,5)
isocinchomeronic acid
2,5-pyridinedicarboxylic acid
IUPAC name
pyridine-2,5-dicarboxylic acid
IUPAC Traditional name
2,5-pyridinedicarboxylic acid
Registration numbers
PubChem CID
7493
PubChem SID
162035080
24888040
24898759
26744319
CAS Number
100-26-5
EC Number
202-834-2
MDL Number
MFCD00006297
Beilstein Number
131697
SureChEMBL Database
SCHEMBL70231
UniProt Database
P0C912
Q812G9
Q7M0J8
P0C8P7
P0C8P9
P0C8P6
Gmelin ID
279305
NMRShiftDB Database
10017791
BindingDB Database
26114
CompTox Database
DTXSID3059210
BRENDA Ligand Database
109069
18192
113677
PubMed Citation Links
16663283
13512348
CHEBI ID
CHEBI:46865
BRENDA Database
1.14.12.15
1.14.11.9
3.5.2.6
2.4.2.19
6.3.5.4
1.14.20.6
1.17.1.8
BKMS React Database
113677
109069
18192
ACToR Database
100-26-5
Reaxys Registry
131697
CHEMBL
CHEMBL88972
Patent number
US2004162317
MetaCyc Database
CPD-14136
Molecule Details
MP Biomedicals
02151986
Purity: 98-99%
05201412
MP Biomedicals Rare Chemical collection
Sigma Aldrich
P63603
Packaging
100 g in poly bottle
TRC
P991640
Used in the preparation of new 2,5-pyridinedicarboxylic acids derivatives as antiviral agents.
ChEBI
CHEBI:46865
A pyridinedicarboxylic acid carrying carboxy groups at positions 2 and 5.
References
PubChem Literature
From Data Sources
•
Flint, D., et al.: J. Biol. Chem., 268, 22369 (1980)
•
Pocker, Y., et al.: Biochemistry, 19, 2045 (1980)
Bioactivity
PubChem BioAssay
Registration numbers
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PubChem CID
•
PubChem SID
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CAS Number
•
EC Number
•
MDL Number
•
Beilstein Number
•
SureChEMBL Database
•
UniProt Database
•
Gmelin ID
•
NMRShiftDB Database
•
BindingDB Database
•
CompTox Database
•
BRENDA Ligand Database
•
PubMed Citation Links
•
CHEBI ID
•
BRENDA Database
•
BKMS React Database
•
ACToR Database
•
Reaxys Registry
•
CHEMBL
•
Patent number
•
MetaCyc Database
Properties
Product Information
Purity
95+%
Source
98-99%
Source
98%
Source
≥98.0% (T)
Source
Certificate of Analysis
Download link
Source
Download link
Source
Download link
Source
Empirical Formula (Hill Notation)
C7H5NO4
Source
Grade
purum
Source
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
false
Source
Room Temperature (15-30°C)
Source
3
Source
36/37/38
Source
26
-
36
Source
H315
-
H319
-
H335
Source
Irritant (Xi)
Warning
Source
dust mask type N95 (US), Eyeshields, Gloves
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
Physical Property
Melting Point
242-247 °C (dec.)(lit.)
Source
Source
Source
TSCA Listed
Storage Condition
German water hazard class
Risk Statements
Safety Statements
GHS Hazard statements
European Hazard Symbols
GHS Signal Word
Personal Protective Equipment
GHS Pictograms
GHS Precautionary statements