13-Phenyltridecanoic acid

Details

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Internal ID 4724cb75-aaaf-4c15-ab66-b5e7a2e0146e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 13-phenyltridecanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H30O2/c20-19(21)17-13-8-6-4-2-1-3-5-7-10-14-18-15-11-9-12-16-18/h9,11-12,15-16H,1-8,10,13-14,17H2,(H,20,21)
InChI Key JVPLVXRNWLOHML-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C19H30O2
Molecular Weight 290.40 g/mol
Exact Mass 290.224580195 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.60
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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20913-07-9
DTXSID70441542
RefChem:78512
DTXCID70392363
13-phenyltridecanoicAcid
13-phenyl tridecanoic acid
13-phenyl-tridecanoic acid
SCHEMBL786517
JVPLVXRNWLOHML-UHFFFAOYSA-N
LMFA01140025
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 13-Phenyltridecanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.5615 56.15%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6227 62.27%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9291 92.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5589 55.89%
P-glycoprotein inhibitior - 0.8187 81.87%
P-glycoprotein substrate - 0.9414 94.14%
CYP3A4 substrate - 0.6692 66.92%
CYP2C9 substrate + 0.8036 80.36%
CYP2D6 substrate - 0.8308 83.08%
CYP3A4 inhibition - 0.9652 96.52%
CYP2C9 inhibition - 0.9243 92.43%
CYP2C19 inhibition - 0.9607 96.07%
CYP2D6 inhibition - 0.9520 95.20%
CYP1A2 inhibition - 0.7992 79.92%
CYP2C8 inhibition - 0.7942 79.42%
CYP inhibitory promiscuity - 0.9697 96.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8146 81.46%
Carcinogenicity (trinary) Non-required 0.6868 68.68%
Eye corrosion - 0.7817 78.17%
Eye irritation + 0.9395 93.95%
Skin irritation + 0.8253 82.53%
Skin corrosion - 0.7852 78.52%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8081 80.81%
Micronuclear - 0.9815 98.15%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.6969 69.69%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6606 66.06%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7719 77.19%
Acute Oral Toxicity (c) III 0.6653 66.53%
Estrogen receptor binding + 0.6295 62.95%
Androgen receptor binding - 0.7601 76.01%
Thyroid receptor binding + 0.6896 68.96%
Glucocorticoid receptor binding - 0.7812 78.12%
Aromatase binding - 0.5095 50.95%
PPAR gamma + 0.8546 85.46%
Honey bee toxicity - 0.9784 97.84%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8474 84.74%

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 96.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.96% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.80% 99.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.14% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.17% 91.11%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.91% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.93% 95.56%
CHEMBL1781 P11387 DNA topoisomerase I 85.10% 97.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.11% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.40% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.61% 94.73%

Plants that contains it

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Cross-Links

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PubChem 10541544
NPASS NPC73840
LOTUS LTS0016854
wikiData Q2823197