Microsphaerodiolin

Details

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Internal ID 4d3128dc-f86d-4241-80e9-647092c5e111
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 10-ethoxy-10-hydroxydeca-6,8-dien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O3/c1-3-15-12(14)10-8-6-4-5-7-9-11(2)13/h4,6,8,10,12,14H,3,5,7,9H2,1-2H3
InChI Key LKYPGHVBAHETHH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O3
Molecular Weight 212.28 g/mol
Exact Mass 212.14124450 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microsphaerodiolin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.6945 69.45%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7344 73.44%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8376 83.76%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5629 56.29%
P-glycoprotein inhibitior - 0.9691 96.91%
P-glycoprotein substrate - 0.9068 90.68%
CYP3A4 substrate - 0.5310 53.10%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.8285 82.85%
CYP3A4 inhibition - 0.9016 90.16%
CYP2C9 inhibition - 0.9315 93.15%
CYP2C19 inhibition - 0.9267 92.67%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.5698 56.98%
CYP2C8 inhibition - 0.9129 91.29%
CYP inhibitory promiscuity - 0.8428 84.28%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6923 69.23%
Carcinogenicity (trinary) Non-required 0.6465 64.65%
Eye corrosion + 0.6063 60.63%
Eye irritation - 0.6827 68.27%
Skin irritation + 0.5450 54.50%
Skin corrosion - 0.7102 71.02%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6166 61.66%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5849 58.49%
skin sensitisation + 0.6955 69.55%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4765 47.65%
Acute Oral Toxicity (c) III 0.7582 75.82%
Estrogen receptor binding - 0.6957 69.57%
Androgen receptor binding - 0.8581 85.81%
Thyroid receptor binding - 0.6298 62.98%
Glucocorticoid receptor binding + 0.6046 60.46%
Aromatase binding - 0.6802 68.02%
PPAR gamma - 0.6347 63.47%
Honey bee toxicity - 0.8774 87.74%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8120 81.20%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.22% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.67% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.13% 97.21%
CHEMBL2581 P07339 Cathepsin D 92.00% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.03% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.02% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.13% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.50% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 82.79% 94.73%

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 139584403
LOTUS LTS0007649
wikiData Q77368411