1-Hydroxy-3,5-dimethoxy-2,4-diprenylxanthone

Details

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Internal ID 229f2ad3-ea6e-4225-aaa1-bba47d048dad
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 1-hydroxy-3,5-dimethoxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3OC)O)C
InChI InChI=1S/C25H28O5/c1-14(2)10-12-17-22(27)20-21(26)16-8-7-9-19(28-5)24(16)30-25(20)18(23(17)29-6)13-11-15(3)4/h7-11,27H,12-13H2,1-6H3
InChI Key KGBJYZXDYBPQGM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O5
Molecular Weight 408.50 g/mol
Exact Mass 408.19367399 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.69
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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3,5-Di-O-methyl-8-deoxygartanin
1-Hydroxy-3,5-dimethoxy-2,4-diprenylxanthone
1-Hydroxy-3,5-dimethoxy-2,4-bis(3-methyl-2-buten-1-yl)-9H-xanthen-9-one
35323-84-3

2D Structure

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2D Structure of 1-Hydroxy-3,5-dimethoxy-2,4-diprenylxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7584 75.84%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6947 69.47%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8911 89.11%
OATP1B3 inhibitior + 0.9374 93.74%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9305 93.05%
P-glycoprotein inhibitior + 0.8907 89.07%
P-glycoprotein substrate - 0.6873 68.73%
CYP3A4 substrate + 0.6047 60.47%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8395 83.95%
CYP2C9 inhibition + 0.6573 65.73%
CYP2C19 inhibition + 0.8891 88.91%
CYP2D6 inhibition - 0.6011 60.11%
CYP1A2 inhibition + 0.8411 84.11%
CYP2C8 inhibition + 0.4628 46.28%
CYP inhibitory promiscuity + 0.7282 72.82%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7515 75.15%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.5333 53.33%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3857 38.57%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7787 77.87%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6956 69.56%
Acute Oral Toxicity (c) III 0.6691 66.91%
Estrogen receptor binding + 0.8714 87.14%
Androgen receptor binding + 0.7059 70.59%
Thyroid receptor binding + 0.5983 59.83%
Glucocorticoid receptor binding + 0.8275 82.75%
Aromatase binding + 0.6129 61.29%
PPAR gamma + 0.9073 90.73%
Honey bee toxicity - 0.8106 81.06%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9924 99.24%

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 98.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.48% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.39% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.65% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.29% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.26% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.93% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.34% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.24% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.24% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.42% 95.50%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.86% 98.11%
CHEMBL2535 P11166 Glucose transporter 84.67% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.47% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.46% 94.03%
CHEMBL1937 Q92769 Histone deacetylase 2 83.17% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.97% 92.62%

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.
Clusia nemorosa

Cross-Links

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PubChem 14777479
LOTUS LTS0052752
wikiData Q105140670