1-(3,7-Dimethylocta-2,6-dienyl)-6,8-dihydroxy-3-(4-hydroxy-3-methylbut-2-enoxy)-2-methoxyxanthen-9-one

Details

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Internal ID f9452b2a-7635-4e37-96bb-ec5cc7b66c89
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1-(3,7-dimethylocta-2,6-dienyl)-6,8-dihydroxy-3-(4-hydroxy-3-methylbut-2-enoxy)-2-methoxyxanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCC1=C2C(=CC(=C1OC)OCC=C(C)CO)OC3=CC(=CC(=C3C2=O)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C2C(=CC(=C1OC)OCC=C(C)CO)OC3=CC(=CC(=C3C2=O)O)O)C)C
InChI InChI=1S/C29H34O7/c1-17(2)7-6-8-18(3)9-10-21-26-24(15-25(29(21)34-5)35-12-11-19(4)16-30)36-23-14-20(31)13-22(32)27(23)28(26)33/h7,9,11,13-15,30-32H,6,8,10,12,16H2,1-5H3
InChI Key AZOVHLSPQFLBKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O7
Molecular Weight 494.60 g/mol
Exact Mass 494.23045342 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.92
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3,7-Dimethylocta-2,6-dienyl)-6,8-dihydroxy-3-(4-hydroxy-3-methylbut-2-enoxy)-2-methoxyxanthen-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 + 0.9023 90.23%
Caco-2 - 0.5910 59.10%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7472 74.72%
OATP2B1 inhibitior - 0.7201 72.01%
OATP1B1 inhibitior + 0.8715 87.15%
OATP1B3 inhibitior + 0.9223 92.23%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7881 78.81%
BSEP inhibitior + 0.9722 97.22%
P-glycoprotein inhibitior + 0.8473 84.73%
P-glycoprotein substrate - 0.5285 52.85%
CYP3A4 substrate + 0.6426 64.26%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8189 81.89%
CYP3A4 inhibition - 0.5772 57.72%
CYP2C9 inhibition - 0.6389 63.89%
CYP2C19 inhibition + 0.6479 64.79%
CYP2D6 inhibition - 0.7207 72.07%
CYP1A2 inhibition + 0.7636 76.36%
CYP2C8 inhibition + 0.7135 71.35%
CYP inhibitory promiscuity + 0.5435 54.35%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7751 77.51%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.7836 78.36%
Skin irritation - 0.7912 79.12%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7202 72.02%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8241 82.41%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7907 79.07%
Acute Oral Toxicity (c) III 0.6182 61.82%
Estrogen receptor binding + 0.8895 88.95%
Androgen receptor binding + 0.7330 73.30%
Thyroid receptor binding + 0.5740 57.40%
Glucocorticoid receptor binding + 0.8842 88.42%
Aromatase binding + 0.7320 73.20%
PPAR gamma + 0.7889 78.89%
Honey bee toxicity - 0.7698 76.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9905 99.05%

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 98.90% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.09% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 93.95% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.89% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 91.54% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.17% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.50% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.80% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.47% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.55% 95.56%
CHEMBL2535 P11166 Glucose transporter 85.25% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.49% 96.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 84.46% 96.12%
CHEMBL3194 P02766 Transthyretin 83.59% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.34% 99.23%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.02% 93.10%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.17% 96.95%
CHEMBL4208 P20618 Proteasome component C5 80.85% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.55% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.53% 99.15%

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 pyrifera

Cross-Links

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PubChem 162893324
LOTUS LTS0193935
wikiData Q104921837