1-Phenyl-2,4-pentadiyne

Details

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Internal ID ac261127-c649-4d27-ade5-058c04a8538f
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name [(2E)-penta-2,4-dienyl]benzene
SMILES (Canonical) C=CC=CCC1=CC=CC=C1
SMILES (Isomeric) C=C/C=C/CC1=CC=CC=C1
InChI InChI=1S/C11H12/c1-2-3-5-8-11-9-6-4-7-10-11/h2-7,9-10H,1,8H2/b5-3+
InChI Key XIKDQDXWYVAHNF-HWKANZROSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12
Molecular Weight 144.21 g/mol
Exact Mass 144.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1-phenyl-2,4-pentadiene
1-Phenyl-2,4-pentadiyne
5-Phenyl-1,3-pentadiene
(2E)-2,4-pentadienylbenzene
(E)-5-Phenyl-1,3-pentadiene
XIKDQDXWYVAHNF-HWKANZROSA-N
[(2E)-penta-2,4-dienyl]-benzene

2D Structure

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2D Structure of 1-Phenyl-2,4-pentadiyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.9618 96.18%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.3588 35.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8147 81.47%
P-glycoprotein inhibitior - 0.9843 98.43%
P-glycoprotein substrate - 0.9664 96.64%
CYP3A4 substrate - 0.7490 74.90%
CYP2C9 substrate - 0.6406 64.06%
CYP2D6 substrate - 0.6571 65.71%
CYP3A4 inhibition - 0.8815 88.15%
CYP2C9 inhibition - 0.8398 83.98%
CYP2C19 inhibition - 0.7143 71.43%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.5690 56.90%
CYP2C8 inhibition - 0.8277 82.77%
CYP inhibitory promiscuity + 0.5175 51.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6264 62.64%
Carcinogenicity (trinary) Warning 0.5257 52.57%
Eye corrosion + 0.9962 99.62%
Eye irritation + 0.9960 99.60%
Skin irritation + 0.9447 94.47%
Skin corrosion + 0.6753 67.53%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6950 69.50%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5574 55.74%
skin sensitisation + 0.9853 98.53%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5769 57.69%
Acute Oral Toxicity (c) III 0.6159 61.59%
Estrogen receptor binding - 0.5744 57.44%
Androgen receptor binding - 0.8791 87.91%
Thyroid receptor binding - 0.7500 75.00%
Glucocorticoid receptor binding - 0.6382 63.82%
Aromatase binding + 0.5410 54.10%
PPAR gamma - 0.4942 49.42%
Honey bee toxicity - 0.6656 66.56%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 0.9762 97.62%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.13% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 91.03% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.47% 98.95%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.40% 93.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.98% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.58% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.02% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.00% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.35% 96.25%

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.
Artemisia capillaris

Cross-Links

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PubChem 11018996
NPASS NPC234704