10-Phenyldecanoic acid

Details

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Internal ID b60fb988-6780-4dc5-9cde-b32df6bf2bd5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 10-phenyldecanoic acid
SMILES (Canonical) C1=CC=C(C=C1)CCCCCCCCCC(=O)O
SMILES (Isomeric) C1=CC=C(C=C1)CCCCCCCCCC(=O)O
InChI InChI=1S/C16H24O2/c17-16(18)14-10-5-3-1-2-4-7-11-15-12-8-6-9-13-15/h6,8-9,12-13H,1-5,7,10-11,14H2,(H,17,18)
InChI Key IISIYJPTBDSIFM-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O2
Molecular Weight 248.36 g/mol
Exact Mass 248.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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18017-73-7
Benzenedecanoic acid
NSC667273
3582F5CN78
NSC-263840
NSC-667273
10-phenyldecanoicacid
SCHEMBL1007173
UNII-3582F5CN78
DTXSID70170921
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 10-Phenyldecanoic 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 + 0.7013 70.13%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6227 62.27%
OATP2B1 inhibitior - 0.8575 85.75%
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 - 0.5288 52.88%
P-glycoprotein inhibitior - 0.8689 86.89%
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 + 0.9505 95.05%
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 + 0.6704 67.04%
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 + 0.6884 68.84%
Androgen receptor binding - 0.7865 78.65%
Thyroid receptor binding + 0.5741 57.41%
Glucocorticoid receptor binding - 0.7849 78.49%
Aromatase binding - 0.5113 51.13%
PPAR gamma + 0.8023 80.23%
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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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.
Acer spicatum
Cephalaria procera
Chamaecytisus hirsutus subsp. hirsutus
Diospyros maritima
Dracaena mannii
Mannia fragrans
Mesua beccariana
Parthenium bipinnatifidum
Pittosporum undulatum
Pongamia pinnata
Rhodanthe propinqua
Tannodia perrieri

Cross-Links

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PubChem 140324
NPASS NPC285173