1,3,7-Trihydroxy-2-(3-hydroxy-3-methylbutyl)xanthen-9-one

Details

Top
Internal ID 777e152f-e617-4f7b-990e-12caa2dee593
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,7-trihydroxy-2-(3-hydroxy-3-methylbutyl)xanthen-9-one
SMILES (Canonical) CC(C)(CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)O
SMILES (Isomeric) CC(C)(CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)O
InChI InChI=1S/C18H18O6/c1-18(2,23)6-5-10-12(20)8-14-15(16(10)21)17(22)11-7-9(19)3-4-13(11)24-14/h3-4,7-8,19-21,23H,5-6H2,1-2H3
InChI Key MPDJBCWZYDZMCW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H18O6
Molecular Weight 330.30 g/mol
Exact Mass 330.11033829 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,3,7-Trihydroxy-2-(3-hydroxy-3-methylbutyl)xanthen-9-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9667 96.67%
Caco-2 - 0.5498 54.98%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7255 72.55%
OATP2B1 inhibitior - 0.5546 55.46%
OATP1B1 inhibitior + 0.8050 80.50%
OATP1B3 inhibitior + 0.9579 95.79%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5499 54.99%
P-glycoprotein inhibitior - 0.8212 82.12%
P-glycoprotein substrate - 0.5664 56.64%
CYP3A4 substrate + 0.5493 54.93%
CYP2C9 substrate - 0.5797 57.97%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition + 0.5957 59.57%
CYP2C9 inhibition - 0.7539 75.39%
CYP2C19 inhibition - 0.7851 78.51%
CYP2D6 inhibition - 0.8086 80.86%
CYP1A2 inhibition + 0.6440 64.40%
CYP2C8 inhibition + 0.6088 60.88%
CYP inhibitory promiscuity - 0.7343 73.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6906 69.06%
Eye corrosion - 0.9916 99.16%
Eye irritation + 0.6365 63.65%
Skin irritation - 0.7066 70.66%
Skin corrosion - 0.8736 87.36%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5933 59.33%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8154 81.54%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.9344 93.44%
Acute Oral Toxicity (c) III 0.6031 60.31%
Estrogen receptor binding + 0.9161 91.61%
Androgen receptor binding + 0.8306 83.06%
Thyroid receptor binding + 0.6322 63.22%
Glucocorticoid receptor binding + 0.9092 90.92%
Aromatase binding + 0.7984 79.84%
PPAR gamma + 0.9453 94.53%
Honey bee toxicity - 0.8605 86.05%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9473 94.73%

Targets

Top

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 98.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.62% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.86% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.02% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.99% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.26% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.60% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.24% 93.99%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 87.33% 90.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.66% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.52% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.01% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.45% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.07% 93.65%

Plants that contains it

Top
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 nigrolineata
Kielmeyera coriacea

Cross-Links

Top
PubChem 15378072
LOTUS LTS0271799
wikiData Q105169409