Umbilicaxanthone B

Details

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Internal ID a78365a7-5158-4f84-8ae2-911a5ab93338
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1,5,7-trihydroxy-4-methoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=CC(=C2C(=C1O)C(=O)C3=C(C(=CC(=C3O2)O)O)CC=C(C)C)OC)C
SMILES (Isomeric) CC(=CCC1=CC(=C2C(=C1O)C(=O)C3=C(C(=CC(=C3O2)O)O)CC=C(C)C)OC)C
InChI InChI=1S/C24H26O6/c1-12(2)6-8-14-10-18(29-5)24-20(21(14)27)22(28)19-15(9-7-13(3)4)16(25)11-17(26)23(19)30-24/h6-7,10-11,25-27H,8-9H2,1-5H3
InChI Key HNEVVGJOTZRWPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.09
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Umbilicaxanthone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9814 98.14%
Caco-2 + 0.4942 49.42%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Nucleus 0.4656 46.56%
OATP2B1 inhibitior - 0.5626 56.26%
OATP1B1 inhibitior + 0.8483 84.83%
OATP1B3 inhibitior + 0.9256 92.56%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6646 66.46%
P-glycoprotein inhibitior + 0.6288 62.88%
P-glycoprotein substrate - 0.7202 72.02%
CYP3A4 substrate + 0.5366 53.66%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7033 70.33%
CYP2C9 inhibition + 0.8037 80.37%
CYP2C19 inhibition + 0.9081 90.81%
CYP2D6 inhibition + 0.7062 70.62%
CYP1A2 inhibition + 0.8876 88.76%
CYP2C8 inhibition + 0.4895 48.95%
CYP inhibitory promiscuity + 0.8928 89.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7089 70.89%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.5322 53.22%
Skin irritation - 0.7476 74.76%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis + 0.5036 50.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4157 41.57%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7854 78.54%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6444 64.44%
Acute Oral Toxicity (c) III 0.6679 66.79%
Estrogen receptor binding + 0.8928 89.28%
Androgen receptor binding + 0.6985 69.85%
Thyroid receptor binding + 0.5442 54.42%
Glucocorticoid receptor binding + 0.8053 80.53%
Aromatase binding + 0.6782 67.82%
PPAR gamma + 0.8965 89.65%
Honey bee toxicity - 0.8045 80.45%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.54% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 93.57% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.21% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.12% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 89.97% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.43% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.64% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.18% 95.56%
CHEMBL3194 P02766 Transthyretin 88.17% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 87.55% 98.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.52% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.66% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.34% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 83.48% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.96% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.81% 94.45%
CHEMBL4208 P20618 Proteasome component C5 80.59% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.13% 91.49%

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.
There are no matching plants.

Cross-Links

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PubChem 21578123
LOTUS LTS0189552
wikiData Q75067162