Capillone

Details

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Internal ID 3d217974-6471-44a6-9002-c287ddf67b88
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name (2E,4E)-1-phenylhexa-2,4-dien-1-one
SMILES (Canonical) CC=CC=CC(=O)C1=CC=CC=C1
SMILES (Isomeric) C/C=C/C=C/C(=O)C1=CC=CC=C1
InChI InChI=1S/C12H12O/c1-2-3-5-10-12(13)11-8-6-4-7-9-11/h2-10H,1H3/b3-2+,10-5+
InChI Key GHNBEBDYYSVNEK-XPQLPGEHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O
Molecular Weight 172.22 g/mol
Exact Mass 172.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(2E,4E)-1-phenyl-2,4-hexadien-1-one
74743-50-3
(2E,4E)-1-phenylhexa-2,4-dien-1-one
SCHEMBL19209055
1-Phenyl-2,4-hexadiene-1-one
CHEBI:80803
(4E)-1-Phenyl-2,4-hexadiene-1-one
(2E,4E)-1-phenyl-hexa-2,4-dien-1-one
C16928
Q27149846

2D Structure

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2D Structure of Capillone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9781 97.81%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5139 51.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9381 93.81%
OATP1B3 inhibitior + 0.9754 97.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6920 69.20%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9810 98.10%
CYP3A4 substrate - 0.7326 73.26%
CYP2C9 substrate - 0.7760 77.60%
CYP2D6 substrate - 0.8636 86.36%
CYP3A4 inhibition - 0.9530 95.30%
CYP2C9 inhibition - 0.9317 93.17%
CYP2C19 inhibition - 0.8185 81.85%
CYP2D6 inhibition - 0.9683 96.83%
CYP1A2 inhibition + 0.5733 57.33%
CYP2C8 inhibition - 0.8208 82.08%
CYP inhibitory promiscuity - 0.6514 65.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5164 51.64%
Carcinogenicity (trinary) Non-required 0.6474 64.74%
Eye corrosion + 0.9865 98.65%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9321 93.21%
Skin corrosion - 0.5427 54.27%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7674 76.74%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.5802 58.02%
skin sensitisation + 0.9821 98.21%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.4588 45.88%
Acute Oral Toxicity (c) III 0.8212 82.12%
Estrogen receptor binding - 0.6055 60.55%
Androgen receptor binding - 0.8254 82.54%
Thyroid receptor binding - 0.7336 73.36%
Glucocorticoid receptor binding - 0.8153 81.53%
Aromatase binding - 0.5054 50.54%
PPAR gamma - 0.8049 80.49%
Honey bee toxicity - 0.9818 98.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8166 81.66%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.97% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.71% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.64% 90.17%
CHEMBL2039 P27338 Monoamine oxidase B 85.29% 92.51%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.03% 95.50%
CHEMBL2581 P07339 Cathepsin D 82.84% 98.95%

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 5315675
NPASS NPC291703
LOTUS LTS0155933
wikiData Q27149846