Fusoxysporone

Details

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Internal ID 662c8e72-617c-42c6-8224-01defc03d85f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,9R,10S)-2,12-dimethyl-6-methylidene-9-propan-2-yltricyclo[8.4.0.01,5]tetradec-11-en-13-one
SMILES (Canonical) CC1CCC2C13CC(=O)C(=CC3C(CCC2=C)C(C)C)C
SMILES (Isomeric) CC1CCC2[C@@]13CC(=O)C(=C[C@@H]3[C@H](CCC2=C)C(C)C)C
InChI InChI=1S/C20H30O/c1-12(2)16-8-6-13(3)17-9-7-15(5)20(17)11-19(21)14(4)10-18(16)20/h10,12,15-18H,3,6-9,11H2,1-2,4-5H3/t15?,16-,17?,18-,20-/m1/s1
InChI Key CCZICCNXBIKTJO-NFKMYMFOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H30O
Molecular Weight 286.50 g/mol
Exact Mass 286.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fusoxysporone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8490 84.90%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4573 45.73%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9009 90.09%
OATP1B3 inhibitior - 0.2794 27.94%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7458 74.58%
P-glycoprotein inhibitior - 0.7332 73.32%
P-glycoprotein substrate - 0.7602 76.02%
CYP3A4 substrate + 0.5584 55.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8670 86.70%
CYP3A4 inhibition - 0.8896 88.96%
CYP2C9 inhibition - 0.8564 85.64%
CYP2C19 inhibition - 0.7586 75.86%
CYP2D6 inhibition - 0.9535 95.35%
CYP1A2 inhibition - 0.7176 71.76%
CYP2C8 inhibition - 0.9343 93.43%
CYP inhibitory promiscuity - 0.8649 86.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5200 52.00%
Eye corrosion - 0.9684 96.84%
Eye irritation - 0.6297 62.97%
Skin irritation + 0.7341 73.41%
Skin corrosion - 0.9710 97.10%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6486 64.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.8323 83.23%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5681 56.81%
Acute Oral Toxicity (c) III 0.6553 65.53%
Estrogen receptor binding - 0.6373 63.73%
Androgen receptor binding + 0.6508 65.08%
Thyroid receptor binding - 0.5068 50.68%
Glucocorticoid receptor binding + 0.5436 54.36%
Aromatase binding - 0.6075 60.75%
PPAR gamma - 0.6178 61.78%
Honey bee toxicity - 0.8075 80.75%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9928 99.28%

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
CHEMBL2581 P07339 Cathepsin D 91.88% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.55% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.48% 94.80%
CHEMBL4072 P07858 Cathepsin B 89.91% 93.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.13% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 87.14% 94.75%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.94% 96.47%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.68% 93.04%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.36% 86.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.02% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.88% 91.11%
CHEMBL1871 P10275 Androgen Receptor 84.79% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.12% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.12% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.52% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.36% 97.09%

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 139584132
LOTUS LTS0270575
wikiData Q77280027