2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5-trihydroxyxanthen-9-one

Details

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Internal ID 6cb51a6f-c498-4093-a4cf-e2bcc744ff5e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 2-(3,7-dimethylocta-2,6-dienyl)-1,3,5-trihydroxyxanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C
InChI InChI=1S/C23H24O5/c1-13(2)6-4-7-14(3)10-11-15-18(25)12-19-20(21(15)26)22(27)16-8-5-9-17(24)23(16)28-19/h5-6,8-10,12,24-26H,4,7,11H2,1-3H3
InChI Key RJLWIAOXQDZMTB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O5
Molecular Weight 380.40 g/mol
Exact Mass 380.16237386 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5-trihydroxyxanthen-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 + 0.9776 97.76%
Caco-2 - 0.8016 80.16%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6480 64.80%
OATP2B1 inhibitior + 0.5757 57.57%
OATP1B1 inhibitior + 0.9095 90.95%
OATP1B3 inhibitior + 0.8983 89.83%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7564 75.64%
BSEP inhibitior + 0.8554 85.54%
P-glycoprotein inhibitior + 0.5956 59.56%
P-glycoprotein substrate - 0.7493 74.93%
CYP3A4 substrate + 0.5969 59.69%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.5430 54.30%
CYP2C9 inhibition + 0.5655 56.55%
CYP2C19 inhibition + 0.6398 63.98%
CYP2D6 inhibition - 0.6968 69.68%
CYP1A2 inhibition + 0.8789 87.89%
CYP2C8 inhibition + 0.4811 48.11%
CYP inhibitory promiscuity + 0.6486 64.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7694 76.94%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.7048 70.48%
Skin irritation - 0.7308 73.08%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7205 72.05%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.7164 71.64%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.9250 92.50%
Acute Oral Toxicity (c) III 0.5435 54.35%
Estrogen receptor binding + 0.9078 90.78%
Androgen receptor binding + 0.6857 68.57%
Thyroid receptor binding + 0.6374 63.74%
Glucocorticoid receptor binding + 0.8663 86.63%
Aromatase binding + 0.7369 73.69%
PPAR gamma + 0.9444 94.44%
Honey bee toxicity - 0.8601 86.01%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.42% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.86% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 97.53% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.61% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.89% 92.08%
CHEMBL1951 P21397 Monoamine oxidase A 93.09% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.03% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.31% 99.23%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.17% 83.57%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.36% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.27% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.47% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.10% 94.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 83.24% 83.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.43% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.75% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.45% 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 mangostana
Garcinia xipshuanbannaensis

Cross-Links

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PubChem 5495932
LOTUS LTS0239053
wikiData Q105237582