1,6,7-Trihydroxy-3-(hydroxymethyl)-2,8-bis(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 15b5f310-77e9-413b-ba45-21974c3ee2c2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1,6,7-trihydroxy-3-(hydroxymethyl)-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C(C2=C(C=C1CO)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C
SMILES (Isomeric) CC(=CCC1=C(C2=C(C=C1CO)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C
InChI InChI=1S/C24H26O6/c1-12(2)5-7-15-14(11-25)9-18-21(23(15)28)24(29)20-16(8-6-13(3)4)22(27)17(26)10-19(20)30-18/h5-6,9-10,25-28H,7-8,11H2,1-4H3
InChI Key HODIDERFBMZRHC-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) 107.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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1,6,7-trihydroxy-3-(hydroxymethyl)-2,8-bis(3-methylbut-2-enyl)xanthen-9-one

2D Structure

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2D Structure of 1,6,7-Trihydroxy-3-(hydroxymethyl)-2,8-bis(3-methylbut-2-enyl)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 + 0.9654 96.54%
Caco-2 - 0.6031 60.31%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7721 77.21%
OATP2B1 inhibitior + 0.5772 57.72%
OATP1B1 inhibitior + 0.8890 88.90%
OATP1B3 inhibitior + 0.9658 96.58%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7233 72.33%
P-glycoprotein inhibitior - 0.4649 46.49%
P-glycoprotein substrate - 0.8238 82.38%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition - 0.7811 78.11%
CYP2C9 inhibition + 0.5939 59.39%
CYP2C19 inhibition + 0.7051 70.51%
CYP2D6 inhibition - 0.6609 66.09%
CYP1A2 inhibition + 0.8623 86.23%
CYP2C8 inhibition - 0.7598 75.98%
CYP inhibitory promiscuity + 0.5456 54.56%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7554 75.54%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.7083 70.83%
Skin irritation - 0.7634 76.34%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4172 41.72%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7825 78.25%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8267 82.67%
Acute Oral Toxicity (c) III 0.6197 61.97%
Estrogen receptor binding + 0.8682 86.82%
Androgen receptor binding + 0.7441 74.41%
Thyroid receptor binding - 0.5379 53.79%
Glucocorticoid receptor binding + 0.7998 79.98%
Aromatase binding + 0.7048 70.48%
PPAR gamma + 0.8787 87.87%
Honey bee toxicity - 0.8835 88.35%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9942 99.42%

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 99.63% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.69% 94.73%
CHEMBL2581 P07339 Cathepsin D 94.28% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.94% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.30% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.50% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.93% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.79% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.92% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.08% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.14% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 81.91% 91.38%
CHEMBL3194 P02766 Transthyretin 81.51% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.04% 98.11%

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.
Hypericum perforatum

Cross-Links

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PubChem 5481476
NPASS NPC263290