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

Details

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Internal ID 08740cea-3abd-442c-96fe-7bcd14575f7d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1-(3,7-dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-7-(4-hydroxy-3-methylbut-2-enyl)-2-methoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H34O7/c1-16(2)7-6-8-17(3)9-12-20-25-23(14-22(32)29(20)35-5)36-24-13-21(31)19(11-10-18(4)15-30)27(33)26(24)28(25)34/h7,9-10,13-14,30-33H,6,8,11-12,15H2,1-5H3
InChI Key BXFCPUCGPCDZKT-UHFFFAOYSA-N
Popularity 7 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) 116.00 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.79
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 9

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)-3,6,8-trihydroxy-7-(4-hydroxy-3-methylbut-2-enyl)-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 + 0.9411 94.11%
Caco-2 - 0.7236 72.36%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7506 75.06%
OATP2B1 inhibitior - 0.5704 57.04%
OATP1B1 inhibitior + 0.9153 91.53%
OATP1B3 inhibitior + 0.8954 89.54%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6631 66.31%
BSEP inhibitior + 0.9202 92.02%
P-glycoprotein inhibitior + 0.8082 80.82%
P-glycoprotein substrate - 0.7565 75.65%
CYP3A4 substrate + 0.5977 59.77%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8189 81.89%
CYP3A4 inhibition + 0.5088 50.88%
CYP2C9 inhibition + 0.5311 53.11%
CYP2C19 inhibition + 0.6863 68.63%
CYP2D6 inhibition - 0.6172 61.72%
CYP1A2 inhibition + 0.8792 87.92%
CYP2C8 inhibition + 0.5092 50.92%
CYP inhibitory promiscuity + 0.5862 58.62%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.8028 80.28%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8347 83.47%
Skin irritation - 0.7904 79.04%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8430 84.30%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8388 83.88%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8861 88.61%
Acute Oral Toxicity (c) III 0.5893 58.93%
Estrogen receptor binding + 0.8543 85.43%
Androgen receptor binding + 0.6864 68.64%
Thyroid receptor binding + 0.5511 55.11%
Glucocorticoid receptor binding + 0.8346 83.46%
Aromatase binding + 0.7174 71.74%
PPAR gamma + 0.7658 76.58%
Honey bee toxicity - 0.7403 74.03%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9938 99.38%

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 99.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.80% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.86% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 92.90% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.59% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.64% 89.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.34% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.14% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.76% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.58% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.88% 96.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.86% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.24% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.52% 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 cowa
Garcinia fusca

Cross-Links

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PubChem 85154683
LOTUS LTS0134888
wikiData Q104947904