Manglexanthone

Details

Top
Internal ID 5029b353-ca9f-412a-b1b0-d89e22ae8392
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 5,8-dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O6/c1-12(2)6-7-14-22-15(10-16(25)23(14)28-5)21(27)19-18(29-22)11-17-13(20(19)26)8-9-24(3,4)30-17/h6,8-11,25-26H,7H2,1-5H3
InChI Key IGOVDGFRUNTYAS-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H24O6
Molecular Weight 408.40 g/mol
Exact Mass 408.15728848 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.06
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
62326-62-9
CHEMBL2437088
XM161786

2D Structure

Top
2D Structure of Manglexanthone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9743 97.43%
Caco-2 + 0.5460 54.60%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6405 64.05%
OATP2B1 inhibitior - 0.5709 57.09%
OATP1B1 inhibitior + 0.8632 86.32%
OATP1B3 inhibitior + 0.9130 91.30%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9486 94.86%
P-glycoprotein inhibitior + 0.7660 76.60%
P-glycoprotein substrate - 0.5348 53.48%
CYP3A4 substrate + 0.6407 64.07%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8288 82.88%
CYP2C9 inhibition + 0.7023 70.23%
CYP2C19 inhibition + 0.8652 86.52%
CYP2D6 inhibition - 0.5195 51.95%
CYP1A2 inhibition + 0.6458 64.58%
CYP2C8 inhibition + 0.5371 53.71%
CYP inhibitory promiscuity + 0.8226 82.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6077 60.77%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7295 72.95%
Skin corrosion - 0.9472 94.72%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4472 44.72%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.5824 58.24%
skin sensitisation - 0.7709 77.09%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.9066 90.66%
Acute Oral Toxicity (c) III 0.6651 66.51%
Estrogen receptor binding + 0.9292 92.92%
Androgen receptor binding + 0.6907 69.07%
Thyroid receptor binding + 0.6820 68.20%
Glucocorticoid receptor binding + 0.9338 93.38%
Aromatase binding + 0.7569 75.69%
PPAR gamma + 0.9269 92.69%
Honey bee toxicity - 0.7115 71.15%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9835 98.35%

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 99.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.24% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.17% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.12% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.09% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.95% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.73% 85.30%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.59% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.57% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 86.85% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.22% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 85.11% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.19% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.51% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.42% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.95% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.60% 92.62%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.64% 89.34%

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.
Tovomita brevistaminea

Cross-Links

Top
PubChem 10001484
LOTUS LTS0049838
wikiData Q105112744