10-O-Methylmacluraxanthone

Details

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Internal ID fb097e02-963d-4beb-baf3-0a46cd77f401
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 5,9-dihydroxy-10-methoxy-2,2-dimethyl-12-(2-methylbut-3-en-2-yl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O6/c1-7-23(2,3)16-19-13(10-11-24(4,5)30-19)18(27)15-17(26)12-8-9-14(25)21(28-6)20(12)29-22(15)16/h7-11,25,27H,1H2,2-6H3
InChI Key XPXBUMXEOVNYQI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O6
Molecular Weight 408.40 g/mol
Exact Mass 408.15728848 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.01
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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5,9-dihydroxy-10-methoxy-2,2-dimethyl-12-(2-methylbut-3-en-2-yl)pyrano(3,2-b)xanthen-6-one
5,9-dihydroxy-10-methoxy-2,2-dimethyl-12-(2-methylbut-3-en-2-yl)pyrano[3,2-b]xanthen-6-one
RefChem:77607
856428-88-1
CHEMBL2147811
SCHEMBL31237288

2D Structure

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2D Structure of 10-O-Methylmacluraxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 + 0.5126 51.26%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6989 69.89%
OATP2B1 inhibitior - 0.7129 71.29%
OATP1B1 inhibitior + 0.8939 89.39%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8249 82.49%
P-glycoprotein inhibitior + 0.7371 73.71%
P-glycoprotein substrate - 0.5683 56.83%
CYP3A4 substrate + 0.6547 65.47%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition + 0.6953 69.53%
CYP2C9 inhibition - 0.8156 81.56%
CYP2C19 inhibition + 0.7089 70.89%
CYP2D6 inhibition - 0.6763 67.63%
CYP1A2 inhibition + 0.6073 60.73%
CYP2C8 inhibition + 0.5897 58.97%
CYP inhibitory promiscuity + 0.5615 56.15%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4872 48.72%
Eye corrosion - 0.9850 98.50%
Eye irritation + 0.6147 61.47%
Skin irritation - 0.7512 75.12%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis + 0.6536 65.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5313 53.13%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7779 77.79%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6804 68.04%
Acute Oral Toxicity (c) III 0.6115 61.15%
Estrogen receptor binding + 0.8650 86.50%
Androgen receptor binding + 0.6231 62.31%
Thyroid receptor binding + 0.8088 80.88%
Glucocorticoid receptor binding + 0.8759 87.59%
Aromatase binding + 0.8086 80.86%
PPAR gamma + 0.8256 82.56%
Honey bee toxicity - 0.7424 74.24%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9773 97.73%

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 99.64% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.37% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 96.37% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.11% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 93.37% 94.75%
CHEMBL2581 P07339 Cathepsin D 91.91% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.00% 89.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.78% 85.30%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 89.47% 80.78%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.93% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.58% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.13% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.38% 94.73%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.81% 92.88%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.86% 99.15%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.42% 95.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.58% 98.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.45% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.37% 100.00%

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 linii
Ilex cornuta

Cross-Links

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PubChem 71458306
NPASS NPC57715
LOTUS LTS0128657
wikiData Q105339038