1,6-Dihydroxy-5-methoxy-7-(3-methylbuta-1,3-dienyl)xanthen-9-one

Details

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Internal ID e1bd9a87-ab65-4313-8c70-ed84e89e6f81
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6-dihydroxy-5-methoxy-7-(3-methylbuta-1,3-dienyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H16O5/c1-10(2)7-8-11-9-12-17(22)15-13(20)5-4-6-14(15)24-18(12)19(23-3)16(11)21/h4-9,20-21H,1H2,2-3H3
InChI Key HWBGGUSOSGUXJQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O5
Molecular Weight 324.30 g/mol
Exact Mass 324.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.96
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,6-Dihydroxy-5-methoxy-7-(3-methylbuta-1,3-dienyl)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 + 0.9799 97.99%
Caco-2 - 0.5240 52.40%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6322 63.22%
OATP2B1 inhibitior - 0.5675 56.75%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior + 0.9813 98.13%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5107 51.07%
P-glycoprotein inhibitior - 0.4450 44.50%
P-glycoprotein substrate - 0.7407 74.07%
CYP3A4 substrate + 0.6004 60.04%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.7341 73.41%
CYP2C9 inhibition + 0.5448 54.48%
CYP2C19 inhibition + 0.9335 93.35%
CYP2D6 inhibition - 0.6763 67.63%
CYP1A2 inhibition + 0.8775 87.75%
CYP2C8 inhibition + 0.6305 63.05%
CYP inhibitory promiscuity + 0.8882 88.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6425 64.25%
Eye corrosion - 0.9798 97.98%
Eye irritation + 0.7822 78.22%
Skin irritation - 0.6671 66.71%
Skin corrosion - 0.9551 95.51%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7286 72.86%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6553 65.53%
skin sensitisation - 0.7505 75.05%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7214 72.14%
Acute Oral Toxicity (c) II 0.4464 44.64%
Estrogen receptor binding + 0.7806 78.06%
Androgen receptor binding + 0.7719 77.19%
Thyroid receptor binding + 0.5817 58.17%
Glucocorticoid receptor binding + 0.8981 89.81%
Aromatase binding + 0.8125 81.25%
PPAR gamma + 0.8250 82.50%
Honey bee toxicity - 0.8516 85.16%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9809 98.09%

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 99.65% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.35% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.27% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.47% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.09% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.76% 93.99%
CHEMBL2581 P07339 Cathepsin D 94.72% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.64% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 92.87% 98.11%
CHEMBL1937 Q92769 Histone deacetylase 2 90.00% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.95% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.62% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 88.01% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.45% 96.00%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 85.62% 88.00%
CHEMBL2535 P11166 Glucose transporter 85.49% 98.75%
CHEMBL3194 P02766 Transthyretin 83.23% 90.71%
CHEMBL3959 P16083 Quinone reductase 2 83.14% 89.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.60% 99.17%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.54% 100.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.39% 80.78%

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.
Symphonia globulifera

Cross-Links

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PubChem 78385682
LOTUS LTS0111163
wikiData Q105034582