Fomitoside A

Details

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Internal ID e3170631-6b93-4d68-8d69-f05699fe6a58
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(2R,3R,4S,5R)-2,4,5-trihydroxyoxan-3-yl] (E,2R)-6-hydroxy-6-methyl-2-[(5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-4-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H54O8/c1-31(2,41)15-8-9-20(29(39)43-28-27(38)24(36)19-42-30(28)40)21-12-17-35(7)23-10-11-25-32(3,4)26(37)14-16-33(25,5)22(23)13-18-34(21,35)6/h8,15,20-21,24-25,27-28,30,36,38,40-41H,9-14,16-19H2,1-7H3/b15-8+/t20-,21-,24-,25+,27+,28-,30-,33-,34-,35+/m1/s1
InChI Key PIXBMLWQDSJWSM-JCGSAEKZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C35H54O8
Molecular Weight 602.80 g/mol
Exact Mass 602.38186868 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fomitoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9076 90.76%
Caco-2 - 0.7615 76.15%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8770 87.70%
OATP2B1 inhibitior - 0.7175 71.75%
OATP1B1 inhibitior + 0.7860 78.60%
OATP1B3 inhibitior + 0.8670 86.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6350 63.50%
BSEP inhibitior + 0.5894 58.94%
P-glycoprotein inhibitior + 0.7352 73.52%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.7238 72.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8802 88.02%
CYP3A4 inhibition - 0.8342 83.42%
CYP2C9 inhibition - 0.7880 78.80%
CYP2C19 inhibition - 0.9073 90.73%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.8491 84.91%
CYP2C8 inhibition + 0.7206 72.06%
CYP inhibitory promiscuity - 0.9289 92.89%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6859 68.59%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9324 93.24%
Skin irritation + 0.5573 55.73%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.5154 51.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4012 40.12%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6766 67.66%
skin sensitisation - 0.9050 90.50%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8478 84.78%
Acute Oral Toxicity (c) III 0.5667 56.67%
Estrogen receptor binding + 0.6983 69.83%
Androgen receptor binding + 0.7225 72.25%
Thyroid receptor binding + 0.5135 51.35%
Glucocorticoid receptor binding + 0.7425 74.25%
Aromatase binding + 0.6798 67.98%
PPAR gamma + 0.5816 58.16%
Honey bee toxicity - 0.7007 70.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9862 98.62%

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 95.91% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.46% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.37% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 92.08% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.66% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.52% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.85% 95.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 87.83% 85.31%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 87.57% 91.24%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.86% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.74% 91.07%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.52% 95.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.00% 91.19%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.24% 96.77%
CHEMBL5028 O14672 ADAM10 84.65% 97.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.54% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.88% 89.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.84% 90.08%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.83% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.67% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.10% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.88% 91.71%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.99% 100.00%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.89% 92.95%
CHEMBL259 P32245 Melanocortin receptor 4 80.65% 95.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.54% 99.17%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.20% 97.28%
CHEMBL1902 P62942 FK506-binding protein 1A 80.17% 97.05%

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 139586367
LOTUS LTS0118870
wikiData Q77505050