4-Pyridoxic Acid

Details

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Internal ID 3a837158-9f87-4b95-ae35-25ac313b9714
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxylic acids
IUPAC Name 3-hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9NO4/c1-4-7(11)6(8(12)13)5(3-10)2-9-4/h2,10-11H,3H2,1H3,(H,12,13)
InChI Key HXACOUQIXZGNBF-UHFFFAOYSA-N
Popularity 325 references in papers

Physical and Chemical Properties

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Molecular Formula C8H9NO4
Molecular Weight 183.16 g/mol
Exact Mass 183.05315777 g/mol
Topological Polar Surface Area (TPSA) 90.70 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.29
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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82-82-6
Pyridoxic acid
4-Pyridoxinic acid
4-Pyridoxylic acid
4-Pyridoxinecarboxylic acid
4-Pyridoxinsaeure
2-Methyl-3-hydroxy-4-carboxy-5-hydroxymethylpyridine
3-hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carboxylic acid
3-Hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinecarboxylic acid
4-Pyridinecarboxylic acid, 3-hydroxy-5-(hydroxymethyl)-2-methyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Pyridoxic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8135 81.35%
Caco-2 - 0.7140 71.40%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7382 73.82%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9008 90.08%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9383 93.83%
P-glycoprotein inhibitior - 0.9648 96.48%
P-glycoprotein substrate - 0.9751 97.51%
CYP3A4 substrate - 0.6016 60.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9144 91.44%
CYP3A4 inhibition - 0.8782 87.82%
CYP2C9 inhibition - 0.9077 90.77%
CYP2C19 inhibition - 0.9389 93.89%
CYP2D6 inhibition - 0.9528 95.28%
CYP1A2 inhibition - 0.9091 90.91%
CYP2C8 inhibition - 0.8313 83.13%
CYP inhibitory promiscuity - 0.8180 81.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8526 85.26%
Carcinogenicity (trinary) Non-required 0.7850 78.50%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.7066 70.66%
Skin irritation - 0.7200 72.00%
Skin corrosion - 0.9489 94.89%
Ames mutagenesis - 0.5367 53.67%
Human Ether-a-go-go-Related Gene inhibition - 0.6441 64.41%
Micronuclear + 0.6274 62.74%
Hepatotoxicity - 0.6571 65.71%
skin sensitisation - 0.8130 81.30%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5931 59.31%
Acute Oral Toxicity (c) IV 0.6217 62.17%
Estrogen receptor binding - 0.7348 73.48%
Androgen receptor binding - 0.7370 73.70%
Thyroid receptor binding - 0.8565 85.65%
Glucocorticoid receptor binding - 0.7051 70.51%
Aromatase binding - 0.7283 72.83%
PPAR gamma - 0.5447 54.47%
Honey bee toxicity - 0.9850 98.50%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.8532 85.32%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.56% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 90.65% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.40% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.78% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.53% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.01% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6723
LOTUS LTS0243263
wikiData Q27102382