1,6-Dihydroxy-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 2e1872d1-9bf0-42af-94a3-14e299d9540e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,6-dihydroxy-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O5/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/h4-7,9,20-21H,8H2,1-3H3
InChI Key KAGMDUVDNXNTNK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O5
Molecular Weight 326.30 g/mol
Exact Mass 326.11542367 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.87
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-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 + 0.9902 99.02%
Caco-2 + 0.5833 58.33%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6139 61.39%
OATP2B1 inhibitior - 0.5666 56.66%
OATP1B1 inhibitior + 0.8942 89.42%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6909 69.09%
P-glycoprotein inhibitior + 0.6358 63.58%
P-glycoprotein substrate - 0.7238 72.38%
CYP3A4 substrate + 0.5686 56.86%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8318 83.18%
CYP2C9 inhibition + 0.8008 80.08%
CYP2C19 inhibition + 0.9328 93.28%
CYP2D6 inhibition + 0.6243 62.43%
CYP1A2 inhibition + 0.8816 88.16%
CYP2C8 inhibition + 0.4578 45.78%
CYP inhibitory promiscuity + 0.8584 85.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7050 70.50%
Eye corrosion - 0.9872 98.72%
Eye irritation + 0.8235 82.35%
Skin irritation - 0.7584 75.84%
Skin corrosion - 0.9595 95.95%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5981 59.81%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation - 0.7942 79.42%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7656 76.56%
Acute Oral Toxicity (c) III 0.6834 68.34%
Estrogen receptor binding + 0.9355 93.55%
Androgen receptor binding + 0.6725 67.25%
Thyroid receptor binding + 0.5384 53.84%
Glucocorticoid receptor binding + 0.9259 92.59%
Aromatase binding + 0.6888 68.88%
PPAR gamma + 0.9124 91.24%
Honey bee toxicity - 0.8867 88.67%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9866 98.66%

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 99.60% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.14% 94.45%
CHEMBL2581 P07339 Cathepsin D 97.42% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.71% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.08% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.52% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 94.29% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.50% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.91% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.89% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.18% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.55% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.90% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.14% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.96% 92.62%
CHEMBL3959 P16083 Quinone reductase 2 84.26% 89.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.81% 96.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.19% 85.30%

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 linii
Symphonia globulifera

Cross-Links

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PubChem 5317658
NPASS NPC126475
LOTUS LTS0057829
wikiData Q105137826