(E)-7-phenylhept-2-en-4,6-diyn-1-ol

Details

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Internal ID 99e722e5-b3d5-4ced-aedc-a952e549fb60
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E)-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#C/C=C/CO
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/b8-3+
InChI Key ZCVJXGJSBVZTMM-FPYGCLRLSA-N
Popularity 1 reference 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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13641-62-8
7-PHENYL-4,6-DIYN-HEPT-2-EN-1-OL
7-Phenyl-2-heptene-4,6-diyn-1-ol
2-Heptene-4,6-diyn-1-ol, 7-phenyl-
1-Hydroxy-7-phenylhept-2-ene-4,6-diyne
SCHEMBL9488087
DTXSID70877105

2D Structure

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2D Structure of (E)-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%

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.
Bidens pilosa
Coreopsis capillacea
Coreopsis nuecensis
Dahlia australis

Cross-Links

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PubChem 6437824
LOTUS LTS0218282
wikiData Q82858835