Staudtiixanthone C

Details

Top
Internal ID 0b4f70e5-1ce9-4100-b54f-3959056471f1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 6,9,11-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one
SMILES (Canonical) CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC(=C4)O)O)C=CC(O2)(C)C)C
SMILES (Isomeric) CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC(=C4)O)O)C=CC(O2)(C)C)C
InChI InChI=1S/C23H22O6/c1-11(2)5-6-13-18(26)17-19(27)15-9-12(24)10-16(25)21(15)28-22(17)14-7-8-23(3,4)29-20(13)14/h5,7-10,24-26H,6H2,1-4H3
InChI Key OCHLEASELDOLFH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C23H22O6
Molecular Weight 394.40 g/mol
Exact Mass 394.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.76
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
6,9,11-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano(2,3-c)xanthen-7-one
6,9,11-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one
RefChem:185383
1186336-47-9
CHEMBL557663

2D Structure

Top
2D Structure of Staudtiixanthone C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 - 0.5254 52.54%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5601 56.01%
OATP2B1 inhibitior - 0.5618 56.18%
OATP1B1 inhibitior + 0.8688 86.88%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8240 82.40%
P-glycoprotein inhibitior + 0.5839 58.39%
P-glycoprotein substrate - 0.5404 54.04%
CYP3A4 substrate + 0.6212 62.12%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8251 82.51%
CYP2C9 inhibition + 0.8142 81.42%
CYP2C19 inhibition + 0.8072 80.72%
CYP2D6 inhibition - 0.7991 79.91%
CYP1A2 inhibition + 0.5412 54.12%
CYP2C8 inhibition + 0.5916 59.16%
CYP inhibitory promiscuity + 0.7730 77.30%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6810 68.10%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.5899 58.99%
Skin irritation - 0.6964 69.64%
Skin corrosion - 0.9120 91.20%
Ames mutagenesis + 0.6199 61.99%
Human Ether-a-go-go-Related Gene inhibition + 0.6550 65.50%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5051 50.51%
skin sensitisation - 0.6575 65.75%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5985 59.85%
Acute Oral Toxicity (c) III 0.6748 67.48%
Estrogen receptor binding + 0.9043 90.43%
Androgen receptor binding + 0.7504 75.04%
Thyroid receptor binding + 0.6127 61.27%
Glucocorticoid receptor binding + 0.9062 90.62%
Aromatase binding + 0.7233 72.33%
PPAR gamma + 0.9088 90.88%
Honey bee toxicity - 0.6517 65.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9878 98.78%

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 99.73% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.05% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 96.48% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.27% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.80% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.40% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 91.33% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.07% 93.99%
CHEMBL3038469 P24941 CDK2/Cyclin A 87.95% 91.38%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.83% 96.12%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.75% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.38% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.29% 95.56%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 87.12% 80.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.67% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.26% 99.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.65% 85.30%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.44% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.93% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.66% 95.89%

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.
Garcinia staudtii

Cross-Links

Top
PubChem 44517665
LOTUS LTS0007606
wikiData Q105189372