Artanin

Details

Top
Internal ID 439c20e3-bb69-45eb-b547-19edbeffc526
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5,7-dimethoxy-8-(3-methylbut-2-enoxy)chromen-2-one
SMILES (Canonical) CC(=CCOC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)C
SMILES (Isomeric) CC(=CCOC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)C
InChI InChI=1S/C16H18O5/c1-10(2)7-8-20-16-13(19-4)9-12(18-3)11-5-6-14(17)21-15(11)16/h5-7,9H,8H2,1-4H3
InChI Key BSOMOYSKROCRIG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H18O5
Molecular Weight 290.31 g/mol
Exact Mass 290.11542367 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
96917-26-9
5,7-Dimethoxy-8-(3-methylbut-2-enoxy)chromen-2-one
5,7-Dimethoxy-8-[(3-methyl-2-buten-1-yl)oxy]-2H-1-benzopyran-2-one
2H-1-Benzopyran-2-one, 5,7-dimethoxy-8-[(3-methyl-2-butenyl)oxy]-
Artain
CHEMBL594165
5,7-Dimethoxy-8-(prenyloxy)coumarin
AKOS032948103
8-(3-Methyl-2-butenyloxy)-5,7-dimethoxycoumarin

2D Structure

Top
2D Structure of Artanin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.9425 94.25%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6969 69.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7831 78.31%
P-glycoprotein inhibitior - 0.4754 47.54%
P-glycoprotein substrate - 0.8110 81.10%
CYP3A4 substrate - 0.5202 52.02%
CYP2C9 substrate - 0.7071 70.71%
CYP2D6 substrate - 0.8388 83.88%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition + 0.5649 56.49%
CYP2C19 inhibition + 0.9422 94.22%
CYP2D6 inhibition - 0.6148 61.48%
CYP1A2 inhibition + 0.9589 95.89%
CYP2C8 inhibition - 0.5575 55.75%
CYP inhibitory promiscuity + 0.8889 88.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7285 72.85%
Eye corrosion - 0.9791 97.91%
Eye irritation + 0.7305 73.05%
Skin irritation - 0.7969 79.69%
Skin corrosion - 0.9771 97.71%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6539 65.39%
Micronuclear - 0.5326 53.26%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.7676 76.76%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6785 67.85%
Acute Oral Toxicity (c) III 0.6862 68.62%
Estrogen receptor binding + 0.7854 78.54%
Androgen receptor binding + 0.7141 71.41%
Thyroid receptor binding + 0.6804 68.04%
Glucocorticoid receptor binding + 0.8332 83.32%
Aromatase binding + 0.7199 71.99%
PPAR gamma + 0.7219 72.19%
Honey bee toxicity - 0.8422 84.22%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9927 99.27%

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 96.77% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.96% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.03% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.94% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.46% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.07% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.39% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 87.14% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.99% 89.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.96% 94.03%
CHEMBL2535 P11166 Glucose transporter 84.10% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.69% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.52% 96.00%
CHEMBL4208 P20618 Proteasome component C5 80.49% 90.00%

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 tanacetifolia
Zanthoxylum nitidum

Cross-Links

Top
PubChem 14841901
NPASS NPC36437
LOTUS LTS0064232
wikiData Q104945339