Fuscaxanthone A

Details

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Internal ID e3e2ac1f-fc2b-41cf-8183-121057bf3dcb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 7-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,9-dihydroxy-8-methoxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)/C)C
InChI InChI=1S/C29H32O6/c1-16(2)8-7-9-17(3)10-11-19-24-22(14-20(30)28(19)33-6)34-23-15-21-18(12-13-29(4,5)35-21)26(31)25(23)27(24)32/h8,10,12-15,30-31H,7,9,11H2,1-6H3/b17-10+
InChI Key XDMFZDJOFFBFDK-LICLKQGHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C29H32O6
Molecular Weight 476.60 g/mol
Exact Mass 476.21988874 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 7.50
Atomic LogP (AlogP) 6.79
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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Fucaxanthone A
CHEMBL3421661
2H,6H-pyrano[3,2-b]xanthen-6-one, 7-[(2E)-3,7-dimethyl-2,6-octadienyl]-5,9-dihydroxy-8-methoxy-2,2-dimethyl-
499777-91-2
5,9-Dihydroxy-8-methoxy-2,2-dimethyl-7-(3,7-dimethyl-2,6-octadienyl)-2H,6H-pyrano[3,2-b]xanthene-6-one
7-(3,7-Dimethyl-octa-2,6-dienyl)-5,9-dihydroxy-8-methoxy-2,2-dimethyl-2H-pyrano[3,2-b]xanthen-6-one
7-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,9-dihydroxy-8-methoxy-2,2-dimethyl-2H,6H-pyrano[3,2-b]xanthen-6-one
InChI=1/C29H32O6/c1-16(2)8-7-9-17(3)10-11-19-24-22(14-20(30)28(19)33-6)34-23-15-21-18(12-13-29(4,5)35-21)26(31)25(23)27(24)32/h8,10,12-15,30-31H,7,9,11H2,1-6H3/b17-10

2D Structure

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2D Structure of Fuscaxanthone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9677 96.77%
Caco-2 - 0.5974 59.74%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7777 77.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8749 87.49%
OATP1B3 inhibitior + 0.8956 89.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7064 70.64%
BSEP inhibitior + 0.9732 97.32%
P-glycoprotein inhibitior + 0.8944 89.44%
P-glycoprotein substrate - 0.5812 58.12%
CYP3A4 substrate + 0.6561 65.61%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.7906 79.06%
CYP2C9 inhibition - 0.5974 59.74%
CYP2C19 inhibition + 0.5538 55.38%
CYP2D6 inhibition - 0.7756 77.56%
CYP1A2 inhibition + 0.6475 64.75%
CYP2C8 inhibition + 0.6018 60.18%
CYP inhibitory promiscuity + 0.5436 54.36%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6930 69.30%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.8137 81.37%
Skin irritation - 0.7282 72.82%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7916 79.16%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5824 58.24%
skin sensitisation - 0.8177 81.77%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.9048 90.48%
Acute Oral Toxicity (c) III 0.5039 50.39%
Estrogen receptor binding + 0.8526 85.26%
Androgen receptor binding + 0.6908 69.08%
Thyroid receptor binding + 0.6142 61.42%
Glucocorticoid receptor binding + 0.8708 87.08%
Aromatase binding + 0.7270 72.70%
PPAR gamma + 0.7636 76.36%
Honey bee toxicity - 0.6714 67.14%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9968 99.68%

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 99.78% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.54% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.53% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.23% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 92.95% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.36% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.69% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.02% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 86.81% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.46% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.25% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.76% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.46% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.24% 99.15%
CHEMBL4208 P20618 Proteasome component C5 82.00% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.56% 91.07%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.09% 80.96%
CHEMBL340 P08684 Cytochrome P450 3A4 80.16% 91.19%

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 cowa
Garcinia dulcis
Garcinia fusca

Cross-Links

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PubChem 5324264
NPASS NPC39091
ChEMBL CHEMBL3421661
LOTUS LTS0109078
wikiData Q104399229