2-(17-Carboxyheptadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

Details

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Internal ID 5ff9afaa-61e5-46d0-b1e2-f16076c18f2f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 2-(17-carboxyheptadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid
SMILES (Canonical) CC1C(C(OC1=O)CCCCCCCCCCCCCCCCCC(=O)O)C(=O)O
SMILES (Isomeric) CC1C(C(OC1=O)CCCCCCCCCCCCCCCCCC(=O)O)C(=O)O
InChI InChI=1S/C24H42O6/c1-19-22(23(27)28)20(30-24(19)29)17-15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18-21(25)26/h19-20,22H,2-18H2,1H3,(H,25,26)(H,27,28)
InChI Key NXYCYXZPBKGGQH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H42O6
Molecular Weight 426.60 g/mol
Exact Mass 426.29813906 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 7.60
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(17-Carboxyheptadecyl)-4-methyl-5-oxooxolane-3-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 + 0.8063 80.63%
Caco-2 - 0.6885 68.85%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8587 85.87%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8988 89.88%
OATP1B3 inhibitior + 0.9547 95.47%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6928 69.28%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.8930 89.30%
CYP3A4 substrate - 0.5690 56.90%
CYP2C9 substrate + 0.6248 62.48%
CYP2D6 substrate - 0.8868 88.68%
CYP3A4 inhibition - 0.8789 87.89%
CYP2C9 inhibition - 0.9337 93.37%
CYP2C19 inhibition - 0.9136 91.36%
CYP2D6 inhibition - 0.9619 96.19%
CYP1A2 inhibition - 0.9362 93.62%
CYP2C8 inhibition - 0.9656 96.56%
CYP inhibitory promiscuity - 0.9832 98.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7011 70.11%
Eye corrosion - 0.9620 96.20%
Eye irritation - 0.5262 52.62%
Skin irritation - 0.6270 62.70%
Skin corrosion - 0.8639 86.39%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6332 63.32%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9489 94.89%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4585 45.85%
Acute Oral Toxicity (c) III 0.6908 69.08%
Estrogen receptor binding + 0.7648 76.48%
Androgen receptor binding - 0.6311 63.11%
Thyroid receptor binding - 0.5980 59.80%
Glucocorticoid receptor binding + 0.6699 66.99%
Aromatase binding - 0.6381 63.81%
PPAR gamma + 0.6497 64.97%
Honey bee toxicity - 0.9720 97.20%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.6888 68.88%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.57% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.98% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.02% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.38% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.65% 99.23%

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 146682621
LOTUS LTS0137735
wikiData Q105187376