Z-6,7-Epoxyligustilide

Details

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Internal ID eb253e43-1219-43c1-bd46-5ce0bfc2d27c
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (4Z)-4-butylidene-1a,2,3,6b-tetrahydrooxireno[2,3-g][2]benzofuran-6-one
SMILES (Canonical) CCCC=C1C2=C(C3C(O3)CC2)C(=O)O1
SMILES (Isomeric) CCC/C=C\1/C2=C(C3C(O3)CC2)C(=O)O1
InChI InChI=1S/C12H14O3/c1-2-3-4-8-7-5-6-9-11(14-9)10(7)12(13)15-8/h4,9,11H,2-3,5-6H2,1H3/b8-4-
InChI Key ZCTBULGQERTBEG-YWEYNIOJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O3
Molecular Weight 206.24 g/mol
Exact Mass 206.094294304 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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106533-40-8
6,7-Epoxyligustilide
SCHEMBL14032224

2D Structure

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2D Structure of Z-6,7-Epoxyligustilide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7825 78.25%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4561 45.61%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9368 93.68%
OATP1B3 inhibitior + 0.9712 97.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7288 72.88%
P-glycoprotein inhibitior - 0.8964 89.64%
P-glycoprotein substrate - 0.9158 91.58%
CYP3A4 substrate - 0.5374 53.74%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.8692 86.92%
CYP3A4 inhibition - 0.8157 81.57%
CYP2C9 inhibition - 0.8121 81.21%
CYP2C19 inhibition - 0.7017 70.17%
CYP2D6 inhibition - 0.8937 89.37%
CYP1A2 inhibition - 0.5839 58.39%
CYP2C8 inhibition - 0.8985 89.85%
CYP inhibitory promiscuity - 0.6710 67.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5351 53.51%
Eye corrosion - 0.8911 89.11%
Eye irritation - 0.5651 56.51%
Skin irritation - 0.6377 63.77%
Skin corrosion - 0.9169 91.69%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6944 69.44%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.5413 54.13%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6483 64.83%
Acute Oral Toxicity (c) III 0.5737 57.37%
Estrogen receptor binding - 0.7690 76.90%
Androgen receptor binding - 0.4939 49.39%
Thyroid receptor binding - 0.5748 57.48%
Glucocorticoid receptor binding - 0.7135 71.35%
Aromatase binding - 0.8893 88.93%
PPAR gamma - 0.5155 51.55%
Honey bee toxicity - 0.9263 92.63%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9131 91.31%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.70% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.37% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.31% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.53% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.23% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.94% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.21% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 82.66% 89.63%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.37% 92.62%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Conioselinum anthriscoides
Daucus carota

Cross-Links

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PubChem 5317139
NPASS NPC131852