1,3,5-Trihydroxy-8-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 624efc27-be0d-486d-b1b2-a32b55858e88
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1,3,5-trihydroxy-8-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C=C1)O)OC3=CC(=CC(=C3C2=O)O)O)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C=C1)O)OC3=CC(=CC(=C3C2=O)O)O)C
InChI InChI=1S/C18H16O5/c1-9(2)3-4-10-5-6-12(20)18-15(10)17(22)16-13(21)7-11(19)8-14(16)23-18/h3,5-8,19-21H,4H2,1-2H3
InChI Key SZMSRIIZCHESKM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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1,3,5-Trihydroxy-8-(3-methylbut-2-enyl)-9H-xanthen-9-one

2D Structure

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2D Structure of 1,3,5-Trihydroxy-8-(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 + 0.9807 98.07%
Caco-2 + 0.7427 74.27%
Blood Brain Barrier - 0.5379 53.79%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5701 57.01%
OATP2B1 inhibitior - 0.5504 55.04%
OATP1B1 inhibitior + 0.8947 89.47%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5973 59.73%
P-glycoprotein inhibitior - 0.7699 76.99%
P-glycoprotein substrate - 0.7564 75.64%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition + 0.7058 70.58%
CYP2C9 inhibition + 0.7476 74.76%
CYP2C19 inhibition + 0.6478 64.78%
CYP2D6 inhibition - 0.5780 57.80%
CYP1A2 inhibition + 0.7679 76.79%
CYP2C8 inhibition + 0.5739 57.39%
CYP inhibitory promiscuity + 0.8767 87.67%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6116 61.16%
Eye corrosion - 0.9856 98.56%
Eye irritation + 0.6484 64.84%
Skin irritation - 0.6662 66.62%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7010 70.10%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation - 0.6442 64.42%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5061 50.61%
Acute Oral Toxicity (c) III 0.7424 74.24%
Estrogen receptor binding + 0.8761 87.61%
Androgen receptor binding + 0.8411 84.11%
Thyroid receptor binding + 0.5862 58.62%
Glucocorticoid receptor binding + 0.9146 91.46%
Aromatase binding + 0.7964 79.64%
PPAR gamma + 0.9502 95.02%
Honey bee toxicity - 0.8757 87.57%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9751 97.51%

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 99.30% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 96.05% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 95.94% 96.12%
CHEMBL2581 P07339 Cathepsin D 92.90% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.93% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 90.67% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.12% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.10% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.94% 95.56%
CHEMBL3194 P02766 Transthyretin 88.10% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.46% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 85.30% 91.38%
CHEMBL4208 P20618 Proteasome component C5 82.95% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.44% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.28% 99.23%

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.
Artemisia anomala
Eupatorium glehnii
Leptochloa digitata
Pinus heldreichii
Piper umbellatum
Senecio brasiliensis
Tovomita krukovii

Cross-Links

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PubChem 5493671
NPASS NPC236428
LOTUS LTS0123554
wikiData Q105264259