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

Details

Top
Internal ID a67a639d-4ddf-44c6-b63a-cbf846f86e14
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,6-trihydroxy-5-methoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C
SMILES (Isomeric) CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C
InChI InChI=1S/C24H26O6/c1-12(2)6-8-14-10-16-22(28)19-18(30-23(16)24(29-5)20(14)26)11-17(25)15(21(19)27)9-7-13(3)4/h6-7,10-11,25-27H,8-9H2,1-5H3
InChI Key JUEOVEHRKOYSOQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.09
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,3,6-Trihydroxy-5-methoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9814 98.14%
Caco-2 - 0.5412 54.12%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Nucleus 0.4656 46.56%
OATP2B1 inhibitior - 0.5599 55.99%
OATP1B1 inhibitior + 0.9160 91.60%
OATP1B3 inhibitior + 0.9256 92.56%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8121 81.21%
P-glycoprotein inhibitior + 0.7263 72.63%
P-glycoprotein substrate - 0.7599 75.99%
CYP3A4 substrate + 0.5618 56.18%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7033 70.33%
CYP2C9 inhibition + 0.8037 80.37%
CYP2C19 inhibition + 0.9081 90.81%
CYP2D6 inhibition + 0.7062 70.62%
CYP1A2 inhibition + 0.8876 88.76%
CYP2C8 inhibition + 0.4604 46.04%
CYP inhibitory promiscuity + 0.8928 89.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7089 70.89%
Eye corrosion - 0.9863 98.63%
Eye irritation + 0.5347 53.47%
Skin irritation - 0.7476 74.76%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4686 46.86%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.6072 60.72%
skin sensitisation - 0.7854 78.54%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8779 87.79%
Acute Oral Toxicity (c) III 0.6679 66.79%
Estrogen receptor binding + 0.9411 94.11%
Androgen receptor binding + 0.6521 65.21%
Thyroid receptor binding + 0.5732 57.32%
Glucocorticoid receptor binding + 0.8430 84.30%
Aromatase binding + 0.6934 69.34%
PPAR gamma + 0.8794 87.94%
Honey bee toxicity - 0.7845 78.45%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.92% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.19% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.01% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.38% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.66% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.58% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.29% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.54% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.44% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.40% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.67% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.98% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.05% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.21% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.71% 96.95%

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.
Calophyllum brasiliense
Maclura tricuspidata

Cross-Links

Top
PubChem 10024541
LOTUS LTS0051617
wikiData Q105135191