(1S,5S,9E,11S,14S)-14-hydroxy-5-methyl-4,15-dioxabicyclo(9.3.1)pentadeca-9,12-dien-3-one

Details

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Internal ID 14adefdb-2414-4dcd-86f1-70d8ecad2729
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1S,5S,9E,11S,14S)-14-hydroxy-5-methyl-4,15-dioxabicyclo[9.3.1]pentadeca-9,12-dien-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O4/c1-10-5-3-2-4-6-11-7-8-12(15)13(18-11)9-14(16)17-10/h4,6-8,10-13,15H,2-3,5,9H2,1H3/b6-4+/t10-,11-,12-,13-/m0/s1
InChI Key LXBFWPWKVZPNRA-NPZYAQMBSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O4
Molecular Weight 252.31 g/mol
Exact Mass 252.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.73
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(+)-asperigillide C
(1S,5S,9E,11S,14S)-14-hydroxy-5-methyl-4,15-dioxabicyclo[9.3.1]pentadeca-9,12-dien-3-one
CHEBI:65452
Q27133896

2D Structure

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2D Structure of (1S,5S,9E,11S,14S)-14-hydroxy-5-methyl-4,15-dioxabicyclo(9.3.1)pentadeca-9,12-dien-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9727 97.27%
Caco-2 + 0.6170 61.70%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5145 51.45%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8852 88.52%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8253 82.53%
P-glycoprotein inhibitior - 0.9411 94.11%
P-glycoprotein substrate - 0.9015 90.15%
CYP3A4 substrate + 0.5085 50.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8591 85.91%
CYP3A4 inhibition - 0.9135 91.35%
CYP2C9 inhibition - 0.9727 97.27%
CYP2C19 inhibition - 0.9277 92.77%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.5889 58.89%
CYP2C8 inhibition - 0.8976 89.76%
CYP inhibitory promiscuity - 0.9889 98.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6370 63.70%
Eye corrosion - 0.9344 93.44%
Eye irritation - 0.9792 97.92%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8684 86.84%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7322 73.22%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.7928 79.28%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.8558 85.58%
Acute Oral Toxicity (c) III 0.5154 51.54%
Estrogen receptor binding - 0.5761 57.61%
Androgen receptor binding - 0.7305 73.05%
Thyroid receptor binding - 0.6591 65.91%
Glucocorticoid receptor binding + 0.5847 58.47%
Aromatase binding - 0.7244 72.44%
PPAR gamma - 0.5686 56.86%
Honey bee toxicity - 0.9387 93.87%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.6684 66.84%

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 91.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.73% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.68% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.12% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.39% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.18% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.00% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.41% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.16% 86.00%

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 24766620
LOTUS LTS0153827
wikiData Q27133896