Illicinole

Details

Top
Internal ID 20566633-05a0-4785-b013-78f558e17b9d
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-(3-methylbut-2-enoxy)-6-prop-2-enyl-1,3-benzodioxole
SMILES (Canonical) CC(=CCOC1=CC2=C(C=C1CC=C)OCO2)C
SMILES (Isomeric) CC(=CCOC1=CC2=C(C=C1CC=C)OCO2)C
InChI InChI=1S/C15H18O3/c1-4-5-12-8-14-15(18-10-17-14)9-13(12)16-7-6-11(2)3/h4,6,8-9H,1,5,7,10H2,2-3H3
InChI Key ZVLUSCHAEWICMZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H18O3
Molecular Weight 246.30 g/mol
Exact Mass 246.125594432 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
5-allyl-6-(3-methylbut-2-enoxy)-1,3-benzodioxole
1,3-Benzodioxole, 5-[(3-methyl-2-butenyl)oxy]-6-(2-propenyl)-

2D Structure

Top
2D Structure of Illicinole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9146 91.46%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7313 73.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9390 93.90%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7424 74.24%
P-glycoprotein inhibitior - 0.8311 83.11%
P-glycoprotein substrate - 0.9271 92.71%
CYP3A4 substrate - 0.5958 59.58%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate + 0.3848 38.48%
CYP3A4 inhibition + 0.8071 80.71%
CYP2C9 inhibition + 0.5415 54.15%
CYP2C19 inhibition + 0.8328 83.28%
CYP2D6 inhibition - 0.5550 55.50%
CYP1A2 inhibition + 0.8004 80.04%
CYP2C8 inhibition - 0.7830 78.30%
CYP inhibitory promiscuity + 0.9062 90.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8748 87.48%
Carcinogenicity (trinary) Non-required 0.5595 55.95%
Eye corrosion - 0.9736 97.36%
Eye irritation + 0.7810 78.10%
Skin irritation - 0.7253 72.53%
Skin corrosion - 0.9168 91.68%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6756 67.56%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.6264 62.64%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6310 63.10%
Acute Oral Toxicity (c) III 0.6698 66.98%
Estrogen receptor binding + 0.7214 72.14%
Androgen receptor binding - 0.7127 71.27%
Thyroid receptor binding + 0.6604 66.04%
Glucocorticoid receptor binding - 0.5582 55.82%
Aromatase binding + 0.6301 63.01%
PPAR gamma + 0.5475 54.75%
Honey bee toxicity - 0.8462 84.62%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.13% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.16% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.23% 96.77%
CHEMBL3401 O75469 Pregnane X receptor 92.17% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.40% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.11% 86.33%
CHEMBL4208 P20618 Proteasome component C5 88.77% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.89% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.43% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.45% 90.24%
CHEMBL2581 P07339 Cathepsin D 83.34% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.89% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.66% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.54% 95.89%

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.
Albizia julibrissin
Anacardium occidentale
Anchusa officinalis
Caryopteris mongholica
Dalbergia rubiginosa
Euphorbia kansui
Illicium arborescens
Illicium verum
Mappia nimmoniana
Mesembryanthemum tortuosum
Satureja atropatana

Cross-Links

Top
PubChem 16729375
NPASS NPC126825
LOTUS LTS0234962
wikiData Q104395663