Picolinic acid

HCID 1018CAS 32075-31-3

Grundinformationen

Standard-SMILES
O=C(O)c1ccccn1
InChIKey
SIOXPEMLGUPBBT-UHFFFAOYSA-N
Summenformel
C6H5NO2
Durchschnittliche Molmasse
123,11 g/mol
Monoisotopische Masse
123,0320284

Überblick

Picolinic acid is a pyridinemonocarboxylic acid in which the carboxy group is located at position 2. It is an intermediate in the metabolism of tryptophan. It has a role as a MALDI matrix material and a human metabolite. It is a conjugate acid of a picolinate.

Namen und Bezeichner

Bevorzugter Name
Picolinic acid
IUPAC
pyridine-2-carboxylic acid
Englischer Name
nikogamol
Summenformel
C6H5NO2
Molmasse
123.1094

Namen und Synonyme

picolinic acid98-98-6Pyridine-2-carboxylic acid2-Pyridinecarboxylic acid2-Carboxypyridineo-Pyridinecarboxylic acidAcide picoliquealpha-Pyridinecarboxylic acid2-pyridine carboxylic acidDTXSID7031903QZV2W997JQDTXCID5011903
Weitere Namen anzeigen
nikogamol
CHEBI:28747RefChem:863115202-719-72-Picolinic acidalpha-Picolinic acidPYRIDINECARBOXYLIC ACIDPyridine-carboxylique-2MFCD00006293

Datenbank-Bezeichner

CAS
32075-31-3、88161-53-9、98-98-6
PubChem CID
1018
DTXSID
DTXSID7031903
ChEMBL
CHEMBL72628
ChEBI
CHEBI:28747
UNII
QZV2W997JQ
EC Number
202-719-7
Nikkaji
J45.682I、J452.014I

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,8
Polarare Oberfläche (TPSA)
50,2 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
1
Schwere Atome
9

Experimentelle und physikochemische Eigenschaften

Chemical ClassesNitrogen Compounds -> Pyridines
DrugsPharmaceuticals -> Listed in ZINC15
SpringerMaterials PropertiesChemical shift
LogP · 2 Einträge

0.72

-1.0

Solubility · 2 Einträge

960 mg/mL at 20 °C

>18.5 [ug/mL] (The mean of the results at pH 7.4)

Melting Point · 2 Einträge

136.5 °C

136.5 °C

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

Danger

H302 (93.9%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 179 reports by companies from 14 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Regulatory Information · 3 Einträge

Chemical: 2-Pyridinecarboxylic acid

Status: Active Update: 03-07-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/24100

2-Pyridinecarboxylic acid: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationEvaluation - Chemicals that are unlikely to require further regulation to manage risks to human health
Hazards SummaryAn eye irritant; [eChemPortal: ERMA] An irritant; [MSDSonline] See Pyridine.
Hazard Classes and CategoriesAcute Tox. 4 (93.9%)

Sicherheit und Schutzausrüstung

Protective Action Criteria (PAC) · 3 Einträge

1.2 [mg/m3]

13 [mg/m3]

78 [mg/m3]

Chemie und Industrie

Pharmakologische Informationen

Pharmacodynamics · 1 Eintrag

PCL-016 or Picolinic acid drug substance is a pyridine carboxylate metabolite of tryptophan. It acts as an anti-infective and immunomodulator through its role in zinc transport. ZFPs are involved in viral replication and packaging as well as normal cell homeostatic functions. Picolinic acid has been shown to be an anti-viral in vitro and in vivo.

Mechanism of ActionAs a therapeutic agent, the molecule works by binding to zinc finger proteins (ZFPs) in a way that changes their structures and disrupts zinc binding, inhibiting function.
MeSH Pharmacological Classification · 1 Eintrag

Organic chemicals that form two or more coordination links with an iron ion. Once coordination has occurred, the complex formed is called a chelate. The iron-binding porphyrin group of hemoglobin is an example of a metal chelate found in biological systems.

Tissue LocationsProstate

Verwendung und Herstellung

Uses · 2 Einträge

Iron-chelating agent that inhibits DNA synthesis; may interfere with iron-dependent production of stable free organic radical which is essential for ribonucleotide reductase formation of deoxyribonucleotides. [ChemIDplus]

Synthetic Polymer MALDI Matrix Compounds

General Manufacturing Information2-Pyridinecarboxylic acid: ACTIVE

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