Cowaxanthone B

Details

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Internal ID 756185d2-10ec-488c-baf3-8c4717d17ebc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1,3-dihydroxy-6,7-dimethoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C(=C3C2=O)CC=C(C)C)OC)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C(=C3C2=O)CC=C(C)C)OC)OC)O)C
InChI InChI=1S/C25H28O6/c1-13(2)7-9-15-17(26)11-18-22(23(15)27)24(28)21-16(10-8-14(3)4)25(30-6)20(29-5)12-19(21)31-18/h7-8,11-12,26-27H,9-10H2,1-6H3
InChI Key BLZDSTHKFQEOIU-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O6
Molecular Weight 424.50 g/mol
Exact Mass 424.18858861 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.39
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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212842-64-3
1,3-dihydroxy-6,7-dimethoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
1,3-Dihydroxy-6,7-dimethoxy-2,8-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one
SCHEMBL3750432
CHEMBL4528420
HY-N6248
AKOS037514945
FS-8123
CS-0032783

2D Structure

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2D Structure of Cowaxanthone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9785 97.85%
Caco-2 + 0.7437 74.37%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Nucleus 0.4867 48.67%
OATP2B1 inhibitior - 0.7153 71.53%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9204 92.04%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7638 76.38%
P-glycoprotein inhibitior + 0.7961 79.61%
P-glycoprotein substrate - 0.7389 73.89%
CYP3A4 substrate + 0.5516 55.16%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7459 74.59%
CYP2C9 inhibition + 0.8385 83.85%
CYP2C19 inhibition + 0.8798 87.98%
CYP2D6 inhibition + 0.7375 73.75%
CYP1A2 inhibition + 0.8864 88.64%
CYP2C8 inhibition + 0.5413 54.13%
CYP inhibitory promiscuity + 0.8747 87.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6989 69.89%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.6217 62.17%
Skin irritation - 0.7533 75.33%
Skin corrosion - 0.9479 94.79%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6998 69.98%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.7707 77.07%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8849 88.49%
Acute Oral Toxicity (c) III 0.6906 69.06%
Estrogen receptor binding + 0.9087 90.87%
Androgen receptor binding + 0.6630 66.30%
Thyroid receptor binding + 0.5534 55.34%
Glucocorticoid receptor binding + 0.8612 86.12%
Aromatase binding + 0.6848 68.48%
PPAR gamma + 0.8848 88.48%
Honey bee toxicity - 0.7401 74.01%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9837 98.37%

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 99.11% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.53% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.51% 94.00%
CHEMBL2581 P07339 Cathepsin D 91.78% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.63% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.25% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.19% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.27% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.39% 89.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.97% 89.34%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.94% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.08% 95.56%
CHEMBL3194 P02766 Transthyretin 83.81% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.64% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.28% 96.95%
CHEMBL1937 Q92769 Histone deacetylase 2 81.28% 94.75%

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.
Cratoxylum arborescens
Garcinia cowa

Cross-Links

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PubChem 11316212
LOTUS LTS0236619
wikiData Q104938273