Artoindonesianin Y

Details

Top
Internal ID 36b40f8e-fee0-42ef-ba84-472f8b013b9e
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 5-(7,7-dimethylfuro[2,3-f]chromen-2-yl)-4,6-bis(3-methylbut-2-enyl)benzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H32O4/c1-17(2)7-10-20-23(30)16-24(31)21(11-8-18(3)4)27(20)26-15-19-9-12-25-22(28(19)32-26)13-14-29(5,6)33-25/h7-9,12-16,30-31H,10-11H2,1-6H3
InChI Key LNBFFYUGHCUNLA-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H32O4
Molecular Weight 444.60 g/mol
Exact Mass 444.23005950 g/mol
Topological Polar Surface Area (TPSA) 62.80 Ų
XlogP 8.10
Atomic LogP (AlogP) 7.71
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
1,3-benzenediol, 5-(7,7-dimethyl-7H-furo[2,3-f][1]benzopyran-2-yl)-4,6-bis(3-methyl-2-butenyl)-
5-(7,7-dimethyl-7H-furo[2,3-f]chromen-2-yl)-4,6-bis(3-methylbut-2-en-1-yl)benzene-1,3-diol
5-(7,7-Dimethyl-7H-furo[2,3-f]chromen-2-yl)-4,6-bis-(3-methyl-but-2-enyl)-benzene-1,3-diol
InChI=1/C29H32O4/c1-17(2)7-10-20-23(30)16-24(31)21(11-8-18(3)4)27(20)26-15-19-9-12-25-22(28(19)32-26)13-14-29(5,6)33-25/h7-9,12-16,30-31H,10-11H2,1-6H

2D Structure

Top
2D Structure of Artoindonesianin Y

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 - 0.5309 53.09%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7506 75.06%
OATP2B1 inhibitior - 0.5698 56.98%
OATP1B1 inhibitior + 0.8484 84.84%
OATP1B3 inhibitior + 0.9096 90.96%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9142 91.42%
P-glycoprotein inhibitior + 0.8470 84.70%
P-glycoprotein substrate - 0.6421 64.21%
CYP3A4 substrate + 0.5465 54.65%
CYP2C9 substrate - 0.6140 61.40%
CYP2D6 substrate - 0.6614 66.14%
CYP3A4 inhibition - 0.7418 74.18%
CYP2C9 inhibition + 0.8479 84.79%
CYP2C19 inhibition + 0.8088 80.88%
CYP2D6 inhibition - 0.8606 86.06%
CYP1A2 inhibition - 0.5218 52.18%
CYP2C8 inhibition + 0.5557 55.57%
CYP inhibitory promiscuity + 0.9304 93.04%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5952 59.52%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.6020 60.20%
Skin irritation - 0.7580 75.80%
Skin corrosion - 0.9197 91.97%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9009 90.09%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.7538 75.38%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6564 65.64%
Acute Oral Toxicity (c) III 0.4637 46.37%
Estrogen receptor binding + 0.9299 92.99%
Androgen receptor binding + 0.8256 82.56%
Thyroid receptor binding + 0.7065 70.65%
Glucocorticoid receptor binding + 0.8147 81.47%
Aromatase binding + 0.7045 70.45%
PPAR gamma + 0.8747 87.47%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9958 99.58%

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 99.52% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.91% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 95.08% 85.30%
CHEMBL2581 P07339 Cathepsin D 93.22% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.16% 94.73%
CHEMBL4208 P20618 Proteasome component C5 91.87% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.46% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.67% 93.99%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.32% 90.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.46% 96.95%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.73% 91.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.39% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.26% 97.21%
CHEMBL1951 P21397 Monoamine oxidase A 80.21% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.04% 89.00%

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.
Artocarpus lacucha

Cross-Links

Top
PubChem 641711
LOTUS LTS0126898
wikiData Q105154252