1-Methylpyridin-1-ium-3-carboxylate--hydrogen chloride (1/1)

Details

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Internal ID 1ff61bfe-2c56-45bf-9806-46a94db4325b
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxylic acids
IUPAC Name 1-methylpyridin-1-ium-3-carboxylate;hydrochloride
SMILES (Canonical) C[N+]1=CC=CC(=C1)C(=O)[O-].Cl
SMILES (Isomeric) C[N+]1=CC=CC(=C1)C(=O)[O-].Cl
InChI InChI=1S/C7H7NO2.ClH/c1-8-4-2-3-6(5-8)7(9)10;/h2-5H,1H3;1H
InChI Key TZSYLWAXZMNUJB-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8ClNO2
Molecular Weight 173.60 g/mol
Exact Mass 173.0243562 g/mol
Topological Polar Surface Area (TPSA) 44.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.70
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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SCHEMBL468365
CHEMBL489961
DTXSID30976921
BDBM50480286
AC-34972
T1429
T-6500
1-Methylpyridin-1-ium-3-carboxylate--hydrogen chloride (1/1)

2D Structure

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2D Structure of 1-Methylpyridin-1-ium-3-carboxylate--hydrogen chloride (1/1)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9028 90.28%
Caco-2 + 0.9665 96.65%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7172 71.72%
OATP2B1 inhibitior - 0.8792 87.92%
OATP1B1 inhibitior + 0.9481 94.81%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9319 93.19%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9629 96.29%
CYP3A4 substrate - 0.7061 70.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8962 89.62%
CYP3A4 inhibition - 0.9592 95.92%
CYP2C9 inhibition - 0.8886 88.86%
CYP2C19 inhibition - 0.9238 92.38%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.7583 75.83%
CYP2C8 inhibition - 0.9398 93.98%
CYP inhibitory promiscuity - 0.9294 92.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6254 62.54%
Carcinogenicity (trinary) Non-required 0.5421 54.21%
Eye corrosion - 0.8264 82.64%
Eye irritation + 0.9809 98.09%
Skin irritation + 0.5552 55.52%
Skin corrosion - 0.6659 66.59%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.9221 92.21%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8353 83.53%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5428 54.28%
Acute Oral Toxicity (c) III 0.4018 40.18%
Estrogen receptor binding - 0.9735 97.35%
Androgen receptor binding - 0.8941 89.41%
Thyroid receptor binding - 0.8732 87.32%
Glucocorticoid receptor binding - 0.9207 92.07%
Aromatase binding - 0.8898 88.98%
PPAR gamma - 0.8170 81.70%
Honey bee toxicity - 0.9838 98.38%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.8040 80.40%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.27% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.35% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.96% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.92% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.51% 96.09%

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.
Abrus precatorius
Achillea millefolium
Astragalus sinicus
Benincasa hispida
Cannabis sativa
Citropsis articulata
Cucurbita moschata
Dictamnus dasycarpus
Lathyrus oleraceus
Medicago sativa
Mirabilis jalapa
Morus alba
Pinellia pedatisecta
Pinellia ternata

Cross-Links

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PubChem 6419886
NPASS NPC159630