7-Phenylhept-2-en-4,6-diyn-1-ol

Details

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Internal ID b49d14f6-4cd6-4d6e-87e4-6edaa8ec2277
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 7-phenylhept-2-en-4,6-diyn-1-ol
SMILES (Canonical) C1=CC=C(C=C1)C#CC#CC=CCO
SMILES (Isomeric) C1=CC=C(C=C1)C#CC#CC=CCO
InChI InChI=1S/C13H10O/c14-12-8-3-1-2-5-9-13-10-6-4-7-11-13/h3-4,6-8,10-11,14H,12H2
InChI Key ZCVJXGJSBVZTMM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O
Molecular Weight 182.22 g/mol
Exact Mass 182.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.59
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Phenylhept-2-en-4,6-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.5983 59.83%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.3809 38.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8960 89.60%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8524 85.24%
P-glycoprotein inhibitior - 0.9741 97.41%
P-glycoprotein substrate - 0.9649 96.49%
CYP3A4 substrate - 0.6900 69.00%
CYP2C9 substrate + 0.6027 60.27%
CYP2D6 substrate - 0.7523 75.23%
CYP3A4 inhibition - 0.8880 88.80%
CYP2C9 inhibition - 0.8131 81.31%
CYP2C19 inhibition - 0.6482 64.82%
CYP2D6 inhibition - 0.9591 95.91%
CYP1A2 inhibition + 0.6991 69.91%
CYP2C8 inhibition - 0.7742 77.42%
CYP inhibitory promiscuity - 0.6255 62.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5444 54.44%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion + 0.8132 81.32%
Eye irritation + 0.7331 73.31%
Skin irritation + 0.8763 87.63%
Skin corrosion + 0.8875 88.75%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7668 76.68%
Micronuclear - 0.7582 75.82%
Hepatotoxicity - 0.6269 62.69%
skin sensitisation + 0.9028 90.28%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.4921 49.21%
Acute Oral Toxicity (c) III 0.5059 50.59%
Estrogen receptor binding + 0.5336 53.36%
Androgen receptor binding - 0.5774 57.74%
Thyroid receptor binding - 0.6832 68.32%
Glucocorticoid receptor binding - 0.5467 54.67%
Aromatase binding + 0.7524 75.24%
PPAR gamma - 0.4934 49.34%
Honey bee toxicity - 0.9476 94.76%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7877 78.77%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 94.24% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.50% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.98% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.95% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.00% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.50% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.28% 96.09%

Cross-Links

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PubChem 114662
NPASS NPC234541
LOTUS LTS0051958
wikiData Q105371746