Compound Summary


quinolinic acid
  Compound Information
 quinolinic acid

Compound Name:

quinolinic acid

Compound CID:

1066

Synonyms:

quinolinic acid

Pyridine-2,3-dicarboxylic acid

2,3-pyridinedicarboxylic acid

89-00-9

quinolinate

More...

Iupac Name:

pyridine-2,3-dicarboxylic acid

InChI:

InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-8-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12)

InChIKey:

GJAWHXHKYYXBSV-UHFFFAOYSA-N

Canonical Smiles:

C1=CC(=C(N=C1)C(=O)O)C(=O)O

Isomeric Smiles:

C1=CC(=C(N=C1)C(=O)O)C(=O)O

Molecular Weight:

167.12

Molecular Formula:

C7H5NO4

  Compound Structure
 2D Structure:
 3D Structure:
  Computed Properties
 quinolinic acid

Molecular Weight:

167.12

Molecular Formula:

C7H5NO4

Hydrogen Bond Donor Count:

2

Hydrogen Bond Acceptor Count:

5

Rotatable Bond Count:

2

Heavy Atom Count:

12

Complexity:

204

  Synonyms
 quinolinic acid

quinolinic acid quinolinic acid

quinolinic acid

Pyridine-2,3-dicarboxylic acid

2,3-pyridinedicarboxylic acid

89-00-9

quinolinate

339155-13-4

Pyridine-2,3-dicarboxylate

UNII-F6F0HK1URN

AI3-63017

2,3-pyridine dicarboxylic acid

pyridine-2,3-carboxylate

MFCD00006295

F6F0HK1URN

CHEMBL286204

CHEBI:16675

2,3-pyridinedicarboxylate

SMR000112287

SR-01000075472

EINECS 201-874-8

NSC 13127

quinolinic-acid

HSDB 7511

2,3-dipicolinic acid

Spectrum_001525

Tocris-0225

pyridinedicarboxylic acid

ACMC-1CIWY

pyridine carboxylate, 6c

Spectrum2_000929

Spectrum3_001502

Spectrum4_000336

Spectrum5_001170

Lopac-P63204

bmse000219

EC 201-874-8

Pyridin-2,3-dicarbonsaeure

DSSTox_CID_21327

DSSTox_RID_79688

DSSTox_GSID_41327

Lopac0_000989

Oprea1_139764

SCHEMBL69230

BSPBio_003143

KBioGR_000711

KBioSS_002005

MLS001332417

MLS001332418

MLS002153210

DivK1c_000773

SPECTRUM1502102

pyridine-2,3-dicarboxlic acid

SPBio_000838

pyridine-5,6-dicarboxylic acid

DTXSID8041327

BDBM26115

HMS502G15

KBio1_000773

KBio2_002005

KBio2_004573

KBio2_007141

KBio3_002643

Quinolinic-4,5,6-d3 Acid

NINDS_000773

HMS1921J12

HMS2267B04

HMS3263E19

HMS3266C15

HMS3411C05

HMS3675C05

HMS3885A17

ZINC331671

NSC13127

NSC18836

Tox21_302051

Tox21_500989

BBL007601

CCG-39677

NSC-13127

NSC-18836

NSC403247

PDSP1_000133

PDSP2_000132

s3624

SBB040573

STK365157

2,3-Pyridinedicarboxylic acid, 99%

AKOS000119760

AM81291

CS-W020665

DB01796

FG-0461

LP00989

LS20272

MCULE-7041185901

NSC-403247

SDCCGMLS-0411909.P028

SDCCGSBI-0050962.P003

CAS-89-00-9

IDI1_000773

MLS-0411909

NCGC00015865-01

NCGC00015865-02

NCGC00015865-03

NCGC00015865-04

NCGC00015865-05

NCGC00015865-06

NCGC00015865-07

NCGC00015865-08

NCGC00015865-12

NCGC00024506-01

NCGC00024506-02

NCGC00024506-03

NCGC00024506-04

NCGC00024506-05

NCGC00024506-06

NCGC00255468-01

NCGC00261674-01

AC-11734

SY003044

2,3-Pyridinedicarboxylic acid (8CI,9CI)

MLS-0411909.P016

DB-016184

HY-100807

B6228

EU-0100989

FT-0609764

FT-0674187

FT-0689818

P0550

ST50213959

2-Propenamide, N-(3-fluorophenyl)methyl-

2,3-Pyridinedicarboxylicacid,labeledwithtritium

89Q009

C03722

D70926

P63204

AC-907/25014157

Q411945

J-019373

Q-201654

SR-01000075472-1

SR-01000075472-3

Z57160166

F2191-0231

2,3-Pyridinedicarboxylic acid, Vetec(TM) reagent grade, 98%

  Experimental Data
 quinolinic acid

Species Dose Unit Control(Avg days) Treatment(Avg days) Avg/Med Lifespan Change(%) Control(Max days) Treatment(Max days) Max Lifespan Change(%) Significant Strain Gender PubMed Avg/Med Lifespan Change tab
Caenorhabditis elegans 33.000000000000000 umol/L 14.000000000000000 NS N2 24134630 Inactive
Caenorhabditis elegans 1.000000000000000 mM -26.000000000000000 S N2 25643626 Inactive
  Experimental Data Visualization
 quinolinic acid

  Statistics Data
 quinolinic acid

Species Avg/Med Lifespan Change(%) Max Lifespan Change(%) Count Reference Count Data point
Caenorhabditis elegans 14.000000000000000 2 2
  Statistics Data Visualization
 quinolinic acid