Capillaridin D

Details

Top
Internal ID 970b7255-be46-4bd0-94ee-d0f6785c39c5
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (Z)-1-phenylhex-1-en-4-yn-3-one
SMILES (Canonical) CC#CC(=O)C=CC1=CC=CC=C1
SMILES (Isomeric) CC#CC(=O)/C=C\C1=CC=CC=C1
InChI InChI=1S/C12H10O/c1-2-6-12(13)10-9-11-7-4-3-5-8-11/h3-5,7-10H,1H3/b10-9-
InChI Key GNWGSNAZSBIJDY-KTKRTIGZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H10O
Molecular Weight 170.21 g/mol
Exact Mass 170.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Capillaridin D

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.9028 90.28%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5154 51.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.9725 97.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8237 82.37%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9787 97.87%
CYP3A4 substrate - 0.7486 74.86%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8396 83.96%
CYP3A4 inhibition - 0.9248 92.48%
CYP2C9 inhibition - 0.8589 85.89%
CYP2C19 inhibition - 0.7660 76.60%
CYP2D6 inhibition - 0.9691 96.91%
CYP1A2 inhibition + 0.6615 66.15%
CYP2C8 inhibition - 0.7555 75.55%
CYP inhibitory promiscuity - 0.5458 54.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5264 52.64%
Carcinogenicity (trinary) Non-required 0.5705 57.05%
Eye corrosion + 0.9564 95.64%
Eye irritation + 0.9517 95.17%
Skin irritation + 0.9049 90.49%
Skin corrosion + 0.6144 61.44%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5936 59.36%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5210 52.10%
skin sensitisation + 0.9669 96.69%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.5839 58.39%
Acute Oral Toxicity (c) III 0.6698 66.98%
Estrogen receptor binding - 0.7460 74.60%
Androgen receptor binding + 0.5575 55.75%
Thyroid receptor binding - 0.6668 66.68%
Glucocorticoid receptor binding - 0.6028 60.28%
Aromatase binding + 0.5446 54.46%
PPAR gamma - 0.8099 80.99%
Honey bee toxicity - 0.9655 96.55%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8633 86.33%

Targets

Top

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.12% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 93.03% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.03% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.92% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.19% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.10% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.46% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.07% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 81.00% 94.73%
CHEMBL5028 O14672 ADAM10 80.75% 97.50%

Plants that contains it

Top
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

Top
PubChem 10725835
LOTUS LTS0256315
wikiData Q105013394