1,5-Dihydroxy-3,6-dimethoxy-4-(3-methylbut-1-en-2-yl)xanthen-9-one

Details

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Internal ID aea4525f-112a-4c89-8b8f-7e0b87d428d6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,5-dihydroxy-3,6-dimethoxy-4-(3-methylbut-1-en-2-yl)xanthen-9-one
SMILES (Canonical) CC(C)C(=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)OC)O)OC
SMILES (Isomeric) CC(C)C(=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)OC)O)OC
InChI InChI=1S/C20H20O6/c1-9(2)10(3)15-14(25-5)8-12(21)16-17(22)11-6-7-13(24-4)18(23)19(11)26-20(15)16/h6-9,21,23H,3H2,1-2,4-5H3
InChI Key HVOHWYIKLLUQDC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,5-Dihydroxy-3,6-dimethoxy-4-(3-methylbut-1-en-2-yl)xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.5235 52.35%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6713 67.13%
OATP2B1 inhibitior - 0.7087 70.87%
OATP1B1 inhibitior + 0.9004 90.04%
OATP1B3 inhibitior + 0.9643 96.43%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4649 46.49%
P-glycoprotein inhibitior + 0.6035 60.35%
P-glycoprotein substrate - 0.5729 57.29%
CYP3A4 substrate + 0.5390 53.90%
CYP2C9 substrate - 0.6020 60.20%
CYP2D6 substrate - 0.8398 83.98%
CYP3A4 inhibition + 0.5845 58.45%
CYP2C9 inhibition + 0.5487 54.87%
CYP2C19 inhibition + 0.9313 93.13%
CYP2D6 inhibition - 0.6375 63.75%
CYP1A2 inhibition + 0.8677 86.77%
CYP2C8 inhibition - 0.5824 58.24%
CYP inhibitory promiscuity + 0.8603 86.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9841 98.41%
Eye irritation + 0.5270 52.70%
Skin irritation - 0.7388 73.88%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.5236 52.36%
Human Ether-a-go-go-Related Gene inhibition - 0.7846 78.46%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7676 76.76%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6381 63.81%
Acute Oral Toxicity (c) III 0.6076 60.76%
Estrogen receptor binding + 0.7093 70.93%
Androgen receptor binding + 0.6676 66.76%
Thyroid receptor binding + 0.7330 73.30%
Glucocorticoid receptor binding + 0.8119 81.19%
Aromatase binding + 0.8095 80.95%
PPAR gamma + 0.8313 83.13%
Honey bee toxicity - 0.8008 80.08%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity + 0.9877 98.77%

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 98.77% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.41% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.49% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 94.45% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.20% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.12% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.30% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.12% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 89.87% 90.20%
CHEMBL3194 P02766 Transthyretin 88.28% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.13% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.12% 85.14%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.92% 93.65%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.88% 89.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.82% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 84.62% 94.73%
CHEMBL2535 P11166 Glucose transporter 84.60% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.38% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 84.16% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.50% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.28% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.22% 99.17%

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.
Garcinia vieillardii

Cross-Links

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PubChem 162870410
LOTUS LTS0215840
wikiData Q105034360