2-(carboxymethyl)-5-oxo-3-tetradecyl-2H-furan-4-carboxylic acid

Details

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Internal ID 72e6a199-5a75-4a64-b040-9d8b353877b5
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 2-(carboxymethyl)-5-oxo-3-tetradecyl-2H-furan-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H34O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-17(15-18(22)23)27-21(26)19(16)20(24)25/h17H,2-15H2,1H3,(H,22,23)(H,24,25)
InChI Key IHEQEJAEFRBTAO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H34O6
Molecular Weight 382.50 g/mol
Exact Mass 382.23553880 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 6.90
Atomic LogP (AlogP) 4.86
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(carboxymethyl)-5-oxo-3-tetradecyl-2H-furan-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9634 96.34%
Caco-2 - 0.5813 58.13%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7352 73.52%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.8745 87.45%
OATP1B3 inhibitior + 0.9610 96.10%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7031 70.31%
P-glycoprotein inhibitior - 0.7388 73.88%
P-glycoprotein substrate - 0.7891 78.91%
CYP3A4 substrate - 0.5664 56.64%
CYP2C9 substrate + 0.6048 60.48%
CYP2D6 substrate - 0.9186 91.86%
CYP3A4 inhibition - 0.6004 60.04%
CYP2C9 inhibition - 0.9006 90.06%
CYP2C19 inhibition - 0.7454 74.54%
CYP2D6 inhibition - 0.9085 90.85%
CYP1A2 inhibition - 0.7657 76.57%
CYP2C8 inhibition - 0.8458 84.58%
CYP inhibitory promiscuity - 0.9020 90.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6354 63.54%
Eye corrosion - 0.9819 98.19%
Eye irritation + 0.7379 73.79%
Skin irritation + 0.6514 65.14%
Skin corrosion - 0.8871 88.71%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4882 48.82%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5523 55.23%
skin sensitisation - 0.8687 86.87%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5087 50.87%
Acute Oral Toxicity (c) III 0.5732 57.32%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5777 57.77%
Thyroid receptor binding - 0.5576 55.76%
Glucocorticoid receptor binding - 0.5148 51.48%
Aromatase binding - 0.7919 79.19%
PPAR gamma + 0.6932 69.32%
Honey bee toxicity - 0.9822 98.22%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6510 65.10%
Fish aquatic toxicity + 0.9814 98.14%

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
CHEMBL2581 P07339 Cathepsin D 92.66% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.13% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.53% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 86.76% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.50% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.06% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.89% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.44% 93.56%

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 85109407
LOTUS LTS0147029
wikiData Q105112960