Cowagarcinone B

Details

Top
Internal ID 3d1ff637-9fc9-4412-b2e3-82fa8330841e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,6-dihydroxy-3,7-dimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)OC)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)OC)OC)C
InChI InChI=1S/C20H20O6/c1-10(2)5-6-11-14(24-3)9-17-18(19(11)22)20(23)12-7-16(25-4)13(21)8-15(12)26-17/h5,7-9,21-22H,6H2,1-4H3
InChI Key VEQACXWBQPLDPZ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methylbut-2-enyl)-xanthone

2D Structure

Top
2D Structure of Cowagarcinone B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.8400 84.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5911 59.11%
OATP2B1 inhibitior - 0.7084 70.84%
OATP1B1 inhibitior + 0.9212 92.12%
OATP1B3 inhibitior + 0.9167 91.67%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7539 75.39%
P-glycoprotein inhibitior + 0.7122 71.22%
P-glycoprotein substrate - 0.6137 61.37%
CYP3A4 substrate + 0.5527 55.27%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8527 85.27%
CYP2C9 inhibition + 0.8359 83.59%
CYP2C19 inhibition + 0.9073 90.73%
CYP2D6 inhibition + 0.6383 63.83%
CYP1A2 inhibition + 0.8818 88.18%
CYP2C8 inhibition + 0.4710 47.10%
CYP inhibitory promiscuity + 0.8382 83.82%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6923 69.23%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.6061 60.61%
Skin irritation - 0.7639 76.39%
Skin corrosion - 0.9597 95.97%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5630 56.30%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.7771 77.71%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.9153 91.53%
Acute Oral Toxicity (c) III 0.7083 70.83%
Estrogen receptor binding + 0.9115 91.15%
Androgen receptor binding + 0.6718 67.18%
Thyroid receptor binding + 0.5808 58.08%
Glucocorticoid receptor binding + 0.9182 91.82%
Aromatase binding + 0.7653 76.53%
PPAR gamma + 0.8816 88.16%
Honey bee toxicity - 0.7590 75.90%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9871 98.71%

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 99.14% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.49% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.45% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.76% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.64% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.30% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.32% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.24% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 88.93% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.41% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.27% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.46% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.53% 92.94%
CHEMBL3194 P02766 Transthyretin 84.53% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.60% 96.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.04% 98.11%

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.
Aster bellidiastrum
Caragana halodendron
Davallia divaricata
Dolomiaea souliei
Eucalyptus camaldulensis
Garcinia cowa
Garcinia dulcis
Garcinia mangostana
Ligularia vellerea
Lonicera hypoleuca
Nicotiana sylvestris
Serpocaulon triseriale

Cross-Links

Top
PubChem 5316764
NPASS NPC283262
LOTUS LTS0269570
wikiData Q105284770