Nicotinic acid,[carboxyl-14C]

Details

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Internal ID cb314f6b-fe83-475a-811e-b45f13c34125
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxylic acids
IUPAC Name pyridine-3-carboxylic acid
SMILES (Canonical) C1=CC(=CN=C1)C(=O)O
SMILES (Isomeric) C1=CC(=CN=C1)[14C](=O)O
InChI InChI=1S/C6H5NO2/c8-6(9)5-2-1-3-7-4-5/h1-4H,(H,8,9)/i6+2
InChI Key PVNIIMVLHYAWGP-ZQBYOMGUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H5NO2
Molecular Weight 125.10 g/mol
Exact Mass 125.03527039 g/mol
Topological Polar Surface Area (TPSA) 50.20 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Nicotinic acid,[carboxyl-14C]
CID 644263
AC1LD8VU
DTXSID30349353
nicotinic acid, [carboxy-14C]-
3-Pyridinecarboxylic-14C acid (9CI)

2D Structure

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2D Structure of Nicotinic acid,[carboxyl-14C]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.8200 82.00%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8256 82.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9538 95.38%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9261 92.61%
P-glycoprotein inhibitior - 0.9904 99.04%
P-glycoprotein substrate - 0.9811 98.11%
CYP3A4 substrate - 0.7673 76.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9155 91.55%
CYP3A4 inhibition - 0.9120 91.20%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.9400 94.00%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.8266 82.66%
CYP inhibitory promiscuity - 0.9875 98.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6742 67.42%
Carcinogenicity (trinary) Non-required 0.6790 67.90%
Eye corrosion - 0.8583 85.83%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9658 96.58%
Skin corrosion - 0.5755 57.55%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8845 88.45%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.6613 66.13%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7853 78.53%
Acute Oral Toxicity (c) IV 0.6559 65.59%
Estrogen receptor binding - 0.9673 96.73%
Androgen receptor binding - 0.9755 97.55%
Thyroid receptor binding - 0.8358 83.58%
Glucocorticoid receptor binding - 0.9254 92.54%
Aromatase binding - 0.8582 85.82%
PPAR gamma - 0.8356 83.56%
Honey bee toxicity - 0.9529 95.29%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.8795 87.95%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3785 Q8TDS4 Hydroxycarboxylic acid receptor 2 8.71 nM
EC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293277 O15118 Niemann-Pick C1 protein 93.72% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 91.45% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.62% 86.33%
CHEMBL2535 P11166 Glucose transporter 83.91% 98.75%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 83.19% 96.47%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.97% 94.62%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.40% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.33% 99.23%
CHEMBL1835 P24557 Thromboxane-A synthase 81.16% 98.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Caltha palustris
Codonopsis pilosula
Eclipta prostrata
Lycium chinense
Lycopodiella cernua
Nicotiana tabacum
Sophora alopecuroides
Trigonella foenum-graecum

Cross-Links

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PubChem 644263
NPASS NPC283923