3-Hexadecen-2-one, 16-phenyl-, (3E)-

Details

Top
Internal ID 1f711b6c-5509-4760-9026-10912955f273
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 16-phenylhexadec-3-en-2-one
SMILES (Canonical) CC(=O)C=CCCCCCCCCCCCCC1=CC=CC=C1
SMILES (Isomeric) CC(=O)C=CCCCCCCCCCCCCC1=CC=CC=C1
InChI InChI=1S/C22H34O/c1-21(23)17-13-10-8-6-4-2-3-5-7-9-11-14-18-22-19-15-12-16-20-22/h12-13,15-17,19-20H,2-11,14,18H2,1H3
InChI Key MRIJVCUMMLLFRJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H34O
Molecular Weight 314.50 g/mol
Exact Mass 314.260965704 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 8.00
Atomic LogP (AlogP) 6.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

Top
828263-24-7
DTXSID60422507

2D Structure

Top
2D Structure of 3-Hexadecen-2-one, 16-phenyl-, (3E)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.7257 72.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Plasma membrane 0.5173 51.73%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6939 69.39%
P-glycoprotein inhibitior - 0.5268 52.68%
P-glycoprotein substrate - 0.8672 86.72%
CYP3A4 substrate - 0.5591 55.91%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.8409 84.09%
CYP3A4 inhibition - 0.9641 96.41%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition - 0.8457 84.57%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition + 0.5345 53.45%
CYP2C8 inhibition - 0.7267 72.67%
CYP inhibitory promiscuity + 0.5104 51.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6028 60.28%
Eye corrosion + 0.9299 92.99%
Eye irritation + 0.8442 84.42%
Skin irritation + 0.6778 67.78%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8298 82.98%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.9104 91.04%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8325 83.25%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6411 64.11%
Acute Oral Toxicity (c) III 0.7772 77.72%
Estrogen receptor binding + 0.6354 63.54%
Androgen receptor binding - 0.6687 66.87%
Thyroid receptor binding + 0.7103 71.03%
Glucocorticoid receptor binding - 0.7763 77.63%
Aromatase binding - 0.4839 48.39%
PPAR gamma + 0.6442 64.42%
Honey bee toxicity - 0.9676 96.76%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9462 94.62%

Targets

Top

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 97.24% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.97% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.53% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.08% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.00% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.36% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.38% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.22% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.09% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.75% 90.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.59% 96.25%

Plants that contains it

Top
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.
Piper auritum

Cross-Links

Top
PubChem 6320306
LOTUS LTS0057139
wikiData Q82234466