Spiciferone E

Details

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Internal ID 06bcf2a3-6d76-47ac-a2b5-3e0994ab7a63
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2R,3R)-6-[(3R)-6-hydroxy-3-methyl-4-oxohexan-3-yl]-2,3-dimethyl-2,3-dihydropyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O4/c1-5-14(4,12(17)6-7-15)13-8-11(16)9(2)10(3)18-13/h8-10,15H,5-7H2,1-4H3/t9-,10-,14+/m1/s1
InChI Key VLRFDSXMCYGPAS-RULNRJAQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O4
Molecular Weight 254.32 g/mol
Exact Mass 254.15180918 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Spiciferone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9792 97.92%
Caco-2 + 0.8917 89.17%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7431 74.31%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.7709 77.09%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.7812 78.12%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9005 90.05%
P-glycoprotein inhibitior - 0.9341 93.41%
P-glycoprotein substrate - 0.7990 79.90%
CYP3A4 substrate - 0.5521 55.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8539 85.39%
CYP3A4 inhibition + 0.6408 64.08%
CYP2C9 inhibition - 0.9242 92.42%
CYP2C19 inhibition - 0.8788 87.88%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.8424 84.24%
CYP2C8 inhibition - 0.9041 90.41%
CYP inhibitory promiscuity - 0.9617 96.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6937 69.37%
Eye corrosion - 0.9847 98.47%
Eye irritation - 0.8835 88.35%
Skin irritation - 0.5825 58.25%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7529 75.29%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6244 62.44%
skin sensitisation - 0.8256 82.56%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6440 64.40%
Acute Oral Toxicity (c) III 0.6783 67.83%
Estrogen receptor binding - 0.5608 56.08%
Androgen receptor binding - 0.5800 58.00%
Thyroid receptor binding - 0.5395 53.95%
Glucocorticoid receptor binding - 0.6845 68.45%
Aromatase binding - 0.6888 68.88%
PPAR gamma - 0.7378 73.78%
Honey bee toxicity - 0.9354 93.54%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.8709 87.09%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.08% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.11% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.61% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.37% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.95% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.41% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.73% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.49% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.25% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.50% 86.92%

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 132596175
LOTUS LTS0052666
wikiData Q105288607