Artocarpetin B

Details

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Internal ID 3da1b5bc-77de-41ab-85ae-76334d8ba0bf
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 5-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)C3=C(C=C(C=C3)O)OC)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)C3=C(C=C(C=C3)O)OC)O)OC)C
InChI InChI=1S/C22H22O6/c1-12(2)5-7-15-19(27-4)10-16(24)21-17(25)11-20(28-22(15)21)14-8-6-13(23)9-18(14)26-3/h5-6,8-11,23-24H,7H2,1-4H3
InChI Key AGQBGLZQKDLJAR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H22O6
Molecular Weight 382.40 g/mol
Exact Mass 382.14163842 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEBI:191800
DTXSID001115569
LMPK12110908
4',5-Dihydroxy-2',7-dimethoxy-8-prenylflavone
8-(gamma,gamma-dimethylallyl)-5,4'-dihydroxy-7,2'-dimethoxyflavone
5-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
170894-22-1
5-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-7-methoxy-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one
5-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-7-methoxy-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one

2D Structure

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2D Structure of Artocarpetin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8406 84.06%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8025 80.25%
OATP2B1 inhibitior - 0.7097 70.97%
OATP1B1 inhibitior + 0.8507 85.07%
OATP1B3 inhibitior + 0.8489 84.89%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7809 78.09%
P-glycoprotein inhibitior + 0.7427 74.27%
P-glycoprotein substrate + 0.5432 54.32%
CYP3A4 substrate + 0.5909 59.09%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7744 77.44%
CYP2C9 inhibition + 0.9095 90.95%
CYP2C19 inhibition + 0.9477 94.77%
CYP2D6 inhibition - 0.6328 63.28%
CYP1A2 inhibition + 0.8370 83.70%
CYP2C8 inhibition + 0.5995 59.95%
CYP inhibitory promiscuity + 0.9465 94.65%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6303 63.03%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.5574 55.74%
Skin irritation - 0.7822 78.22%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4830 48.30%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8334 83.34%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.4554 45.54%
Acute Oral Toxicity (c) III 0.7450 74.50%
Estrogen receptor binding + 0.9157 91.57%
Androgen receptor binding + 0.8527 85.27%
Thyroid receptor binding + 0.6542 65.42%
Glucocorticoid receptor binding + 0.8498 84.98%
Aromatase binding + 0.8042 80.42%
PPAR gamma + 0.9029 90.29%
Honey bee toxicity - 0.7280 72.80%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9919 99.19%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.66% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.16% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.01% 98.95%
CHEMBL3194 P02766 Transthyretin 94.05% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.10% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.09% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.90% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.84% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.26% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 90.06% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.85% 89.00%
CHEMBL2535 P11166 Glucose transporter 83.91% 98.75%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.81% 97.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.93% 85.14%
CHEMBL4208 P20618 Proteasome component C5 82.28% 90.00%
CHEMBL301 P24941 Cyclin-dependent kinase 2 80.68% 91.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.59% 99.15%

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.
Artocarpus heterophyllus

Cross-Links

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PubChem 15231525
LOTUS LTS0265584
wikiData Q104911976