Umbilicaxanthoside B

Details

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Internal ID f14d68b9-6d22-45dd-84d7-df0847256e3a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 7-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,5-dihydroxy-4-methoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H46O16/c1-14(2)6-8-16-10-20(47-5)33-24(25(16)40)28(43)23-17(9-7-15(3)4)19(11-18(39)32(23)51-33)48-36-31(46)34(27(42)22(13-38)50-36)52-35-30(45)29(44)26(41)21(12-37)49-35/h6-7,10-11,21-22,26-27,29-31,34-42,44-46H,8-9,12-13H2,1-5H3
InChI Key OWQFOQSOJROWAG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H46O16
Molecular Weight 734.70 g/mol
Exact Mass 734.27858538 g/mol
Topological Polar Surface Area (TPSA) 255.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 16
H-Bond Donor 9
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Umbilicaxanthoside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7661 76.61%
Caco-2 - 0.8822 88.22%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5833 58.33%
OATP2B1 inhibitior - 0.5785 57.85%
OATP1B1 inhibitior + 0.8351 83.51%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6831 68.31%
P-glycoprotein inhibitior + 0.6484 64.84%
P-glycoprotein substrate - 0.5665 56.65%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate - 0.8387 83.87%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.9611 96.11%
CYP2C9 inhibition - 0.7963 79.63%
CYP2C19 inhibition - 0.6586 65.86%
CYP2D6 inhibition - 0.7832 78.32%
CYP1A2 inhibition - 0.6994 69.94%
CYP2C8 inhibition + 0.6203 62.03%
CYP inhibitory promiscuity - 0.6911 69.11%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7319 73.19%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9112 91.12%
Skin irritation - 0.8088 80.88%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis + 0.5536 55.36%
Human Ether-a-go-go-Related Gene inhibition + 0.7132 71.32%
Micronuclear - 0.5567 55.67%
Hepatotoxicity - 0.6217 62.17%
skin sensitisation - 0.8419 84.19%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6952 69.52%
Acute Oral Toxicity (c) III 0.6661 66.61%
Estrogen receptor binding + 0.8170 81.70%
Androgen receptor binding + 0.6381 63.81%
Thyroid receptor binding - 0.4909 49.09%
Glucocorticoid receptor binding + 0.6127 61.27%
Aromatase binding + 0.6418 64.18%
PPAR gamma + 0.7109 71.09%
Honey bee toxicity - 0.6707 67.07%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9490 94.90%

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 99.83% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.91% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.43% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.94% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.78% 89.34%
CHEMBL2581 P07339 Cathepsin D 91.96% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.91% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.06% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.53% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.12% 95.56%
CHEMBL3194 P02766 Transthyretin 85.09% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.48% 92.94%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 84.41% 95.64%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.57% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.69% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.67% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.32% 92.62%
CHEMBL1255126 O15151 Protein Mdm4 81.13% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.50% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139584136
LOTUS LTS0146443
wikiData Q77280063