Arecaidine

Details

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Internal ID 09dabfb7-958b-405b-a7a0-c67ccd1937a8
Taxonomy Alkaloids and derivatives
IUPAC Name 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylic acid
SMILES (Canonical) CN1CCC=C(C1)C(=O)O
SMILES (Isomeric) CN1CCC=C(C1)C(=O)O
InChI InChI=1S/C7H11NO2/c1-8-4-2-3-6(5-8)7(9)10/h3H,2,4-5H2,1H3,(H,9,10)
InChI Key DNJFTXKSFAMXQF-UHFFFAOYSA-N
Popularity 71 references in papers

Physical and Chemical Properties

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Molecular Formula C7H11NO2
Molecular Weight 141.17 g/mol
Exact Mass 141.078978594 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP -2.30
Atomic LogP (AlogP) 0.33
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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499-04-7
Arecaine
Methylguvacine
1-Methyl-1,2,5,6-tetrahydropyridine-3-carboxylic acid
N-Methylguvacine
1,2,5,6-Tetrahydro-1-methylnicotinic acid
1-methyl-3,6-dihydro-2H-pyridine-5-carboxylic acid
NSC 76017
1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarboxylic acid
UNII-0S8YEV0D4O
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Arecaidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9342 93.42%
Caco-2 + 0.9304 93.04%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5707 57.07%
OATP2B1 inhibitior - 0.8414 84.14%
OATP1B1 inhibitior + 0.9708 97.08%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.9381 93.81%
P-glycoprotein inhibitior - 0.9903 99.03%
P-glycoprotein substrate - 0.9348 93.48%
CYP3A4 substrate - 0.7739 77.39%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7692 76.92%
CYP3A4 inhibition - 0.9921 99.21%
CYP2C9 inhibition - 0.8412 84.12%
CYP2C19 inhibition - 0.8728 87.28%
CYP2D6 inhibition - 0.9592 95.92%
CYP1A2 inhibition - 0.6542 65.42%
CYP2C8 inhibition - 0.9914 99.14%
CYP inhibitory promiscuity - 0.9919 99.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6436 64.36%
Eye corrosion - 0.8522 85.22%
Eye irritation + 0.9435 94.35%
Skin irritation + 0.5381 53.81%
Skin corrosion - 0.6277 62.77%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8259 82.59%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.7338 73.38%
skin sensitisation - 0.7828 78.28%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.6192 61.92%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.5870 58.70%
Acute Oral Toxicity (c) III 0.6905 69.05%
Estrogen receptor binding - 0.9706 97.06%
Androgen receptor binding - 0.7598 75.98%
Thyroid receptor binding - 0.9402 94.02%
Glucocorticoid receptor binding - 0.9282 92.82%
Aromatase binding - 0.9135 91.35%
PPAR gamma - 0.8809 88.09%
Honey bee toxicity - 0.9854 98.54%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.6545 65.45%

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 95.86% 96.09%
CHEMBL4208 P20618 Proteasome component C5 94.43% 90.00%
CHEMBL2581 P07339 Cathepsin D 91.31% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.03% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.91% 85.14%

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.
Areca catechu

Cross-Links

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PubChem 10355
NPASS NPC305973
LOTUS LTS0048904
wikiData Q9159393