1-Phenylhept-5-ene-1,3-diyne

Details

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Internal ID 54663af8-3a66-4292-b0fd-dbe8bb817079
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name hept-5-en-1,3-diynylbenzene
SMILES (Canonical) CC=CC#CC#CC1=CC=CC=C1
SMILES (Isomeric) CC=CC#CC#CC1=CC=CC=C1
InChI InChI=1S/C13H10/c1-2-3-4-5-7-10-13-11-8-6-9-12-13/h2-3,6,8-9,11-12H,1H3
InChI Key OQOPFMDMSRLRRH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10
Molecular Weight 166.22 g/mol
Exact Mass 166.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Phenylhept-5-ene-1,3-diyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.8289 82.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4508 45.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.9676 96.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8300 83.00%
P-glycoprotein inhibitior - 0.9753 97.53%
P-glycoprotein substrate - 0.9587 95.87%
CYP3A4 substrate - 0.6871 68.71%
CYP2C9 substrate - 0.6057 60.57%
CYP2D6 substrate - 0.7897 78.97%
CYP3A4 inhibition - 0.9225 92.25%
CYP2C9 inhibition - 0.7855 78.55%
CYP2C19 inhibition - 0.8837 88.37%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition + 0.5065 50.65%
CYP2C8 inhibition - 0.8010 80.10%
CYP inhibitory promiscuity - 0.5686 56.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5664 56.64%
Carcinogenicity (trinary) Warning 0.4093 40.93%
Eye corrosion + 0.9868 98.68%
Eye irritation + 0.9474 94.74%
Skin irritation + 0.9345 93.45%
Skin corrosion + 0.6697 66.97%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7500 75.00%
Micronuclear - 0.9541 95.41%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation + 0.9740 97.40%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6393 63.93%
Acute Oral Toxicity (c) III 0.8809 88.09%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.6509 65.09%
Thyroid receptor binding - 0.6567 65.67%
Glucocorticoid receptor binding - 0.6030 60.30%
Aromatase binding + 0.6010 60.10%
PPAR gamma - 0.6322 63.22%
Honey bee toxicity - 0.9262 92.62%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9639 96.39%

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 96.96% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.01% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 89.34% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.09% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.59% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.96% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 81.42% 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.
Bidens pilosa
Coreopsis capillacea
Dahlia sherffii

Cross-Links

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PubChem 117403
LOTUS LTS0111287
wikiData Q105197070