2-(5-Hexadeca-9,11,13-trienyl-3,5-dimethyldioxolan-3-yl)acetic acid

Details

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Internal ID 2b37704c-d41f-4f0d-be1c-0f7cdd1a3237
Taxonomy Organoheterocyclic compounds > Dioxolanes > 1,2-dioxolanes
IUPAC Name 2-(5-hexadeca-9,11,13-trienyl-3,5-dimethyldioxolan-3-yl)acetic acid
SMILES (Canonical) CCC=CC=CC=CCCCCCCCCC1(CC(OO1)(C)CC(=O)O)C
SMILES (Isomeric) CCC=CC=CC=CCCCCCCCCC1(CC(OO1)(C)CC(=O)O)C
InChI InChI=1S/C23H38O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22(2)20-23(3,27-26-22)19-21(24)25/h5-10H,4,11-20H2,1-3H3,(H,24,25)
InChI Key MIXTVNJOFJIRKQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H38O4
Molecular Weight 378.50 g/mol
Exact Mass 378.27700969 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.53
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(5-Hexadeca-9,11,13-trienyl-3,5-dimethyldioxolan-3-yl)acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9681 96.81%
Caco-2 + 0.5188 51.88%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5088 50.88%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8508 85.08%
OATP1B3 inhibitior + 0.9093 90.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9402 94.02%
P-glycoprotein inhibitior - 0.4882 48.82%
P-glycoprotein substrate - 0.8330 83.30%
CYP3A4 substrate + 0.5236 52.36%
CYP2C9 substrate + 0.7919 79.19%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition - 0.7894 78.94%
CYP2C9 inhibition - 0.7929 79.29%
CYP2C19 inhibition - 0.7999 79.99%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition - 0.6568 65.68%
CYP2C8 inhibition - 0.7584 75.84%
CYP inhibitory promiscuity - 0.9127 91.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6145 61.45%
Eye corrosion - 0.9387 93.87%
Eye irritation - 0.8736 87.36%
Skin irritation + 0.5212 52.12%
Skin corrosion - 0.9065 90.65%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6476 64.76%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7047 70.47%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6196 61.96%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6531 65.31%
Acute Oral Toxicity (c) III 0.5458 54.58%
Estrogen receptor binding + 0.8103 81.03%
Androgen receptor binding + 0.6354 63.54%
Thyroid receptor binding + 0.7210 72.10%
Glucocorticoid receptor binding + 0.8450 84.50%
Aromatase binding + 0.7099 70.99%
PPAR gamma + 0.6729 67.29%
Honey bee toxicity - 0.9563 95.63%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6150 61.50%
Fish aquatic toxicity + 0.9405 94.05%

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 95.33% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.84% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 92.11% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.46% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.99% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.15% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.38% 96.38%

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 85050404
LOTUS LTS0235689
wikiData Q105165272