1,3,6-Trihydroxy-7-methoxy-2-(3,7-dimethyl-2,6-octadienyl)xanthone

Details

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Internal ID c5fd603b-c512-4cfb-85b7-5acdc38d981d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 2-(3,7-dimethylocta-2,6-dienyl)-1,3,6-trihydroxy-7-methoxyxanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C=C3C2=O)OC)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C=C3C2=O)OC)O)O)C)C
InChI InChI=1S/C24H26O6/c1-13(2)6-5-7-14(3)8-9-15-17(25)11-21-22(23(15)27)24(28)16-10-20(29-4)18(26)12-19(16)30-21/h6,8,10-12,25-27H,5,7,9H2,1-4H3
InChI Key VEGUCVDYIMCIAZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,6-Trihydroxy-7-methoxy-2-(3,7-dimethyl-2,6-octadienyl)xanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9746 97.46%
Caco-2 - 0.5742 57.42%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6546 65.46%
OATP2B1 inhibitior - 0.7026 70.26%
OATP1B1 inhibitior + 0.9111 91.11%
OATP1B3 inhibitior + 0.8857 88.57%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7314 73.14%
BSEP inhibitior + 0.9042 90.42%
P-glycoprotein inhibitior + 0.7160 71.60%
P-glycoprotein substrate - 0.6998 69.98%
CYP3A4 substrate + 0.5901 59.01%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.5765 57.65%
CYP2C9 inhibition + 0.5528 55.28%
CYP2C19 inhibition + 0.7038 70.38%
CYP2D6 inhibition - 0.5804 58.04%
CYP1A2 inhibition + 0.8554 85.54%
CYP2C8 inhibition + 0.5483 54.83%
CYP inhibitory promiscuity + 0.6676 66.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7819 78.19%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.6379 63.79%
Skin irritation - 0.7769 77.69%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis + 0.5046 50.46%
Human Ether-a-go-go-Related Gene inhibition + 0.7707 77.07%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.7865 78.65%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.9312 93.12%
Acute Oral Toxicity (c) III 0.5079 50.79%
Estrogen receptor binding + 0.9174 91.74%
Androgen receptor binding + 0.6706 67.06%
Thyroid receptor binding + 0.6431 64.31%
Glucocorticoid receptor binding + 0.9296 92.96%
Aromatase binding + 0.7502 75.02%
PPAR gamma + 0.8737 87.37%
Honey bee toxicity - 0.7444 74.44%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9969 99.69%

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 99.32% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.48% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.25% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.18% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.04% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.65% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.59% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.31% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.26% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.38% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.48% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.31% 92.94%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.16% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.24% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.83% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.75% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.61% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.87% 95.50%

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 cowa
Garcinia dulcis
Garcinia fusca

Cross-Links

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PubChem 85128675
LOTUS LTS0095851
wikiData Q105284586