(1S,4S,6S,10R,14E)-14-[(E)-4-hydroperoxy-4-methylpent-2-enylidene]-4-methyl-9-methylidene-5,12-dioxatricyclo[8.4.0.04,6]tetradecan-11-one

Details

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Internal ID 89a68b05-cdbb-4734-824d-21bb7e72714e
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name (1S,4S,6S,10R,14E)-14-[(E)-4-hydroperoxy-4-methylpent-2-enylidene]-4-methyl-9-methylidene-5,12-dioxatricyclo[8.4.0.04,6]tetradecan-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28O5/c1-13-7-8-16-20(4,24-16)11-9-15-14(12-23-18(21)17(13)15)6-5-10-19(2,3)25-22/h5-6,10,15-17,22H,1,7-9,11-12H2,2-4H3/b10-5+,14-6-/t15-,16+,17+,20+/m1/s1
InChI Key LYNQLUCBGBCZBC-YXWCGTORSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O5
Molecular Weight 348.40 g/mol
Exact Mass 348.19367399 g/mol
Topological Polar Surface Area (TPSA) 68.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4S,6S,10R,14E)-14-[(E)-4-hydroperoxy-4-methylpent-2-enylidene]-4-methyl-9-methylidene-5,12-dioxatricyclo[8.4.0.04,6]tetradecan-11-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9576 95.76%
Caco-2 + 0.5727 57.27%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7373 73.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8879 88.79%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9041 90.41%
P-glycoprotein inhibitior - 0.7055 70.55%
P-glycoprotein substrate - 0.7283 72.83%
CYP3A4 substrate + 0.6774 67.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.6936 69.36%
CYP2C9 inhibition - 0.7378 73.78%
CYP2C19 inhibition - 0.7485 74.85%
CYP2D6 inhibition - 0.9025 90.25%
CYP1A2 inhibition - 0.5743 57.43%
CYP2C8 inhibition + 0.4820 48.20%
CYP inhibitory promiscuity - 0.9511 95.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6534 65.34%
Eye corrosion - 0.9727 97.27%
Eye irritation - 0.9398 93.98%
Skin irritation - 0.6870 68.70%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.5479 54.79%
Human Ether-a-go-go-Related Gene inhibition - 0.5478 54.78%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.6544 65.44%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6074 60.74%
Acute Oral Toxicity (c) III 0.6264 62.64%
Estrogen receptor binding + 0.8114 81.14%
Androgen receptor binding + 0.5626 56.26%
Thyroid receptor binding + 0.7892 78.92%
Glucocorticoid receptor binding + 0.8376 83.76%
Aromatase binding + 0.5284 52.84%
PPAR gamma + 0.6574 65.74%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9769 97.69%

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 97.58% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.41% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.09% 94.45%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.56% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.37% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.79% 86.33%
CHEMBL230 P35354 Cyclooxygenase-2 89.66% 89.63%
CHEMBL3922 P50579 Methionine aminopeptidase 2 88.04% 97.28%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.76% 93.04%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.61% 90.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.31% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.05% 100.00%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 85.02% 94.78%
CHEMBL340 P08684 Cytochrome P450 3A4 83.85% 91.19%
CHEMBL2581 P07339 Cathepsin D 83.73% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.14% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.82% 92.62%
CHEMBL259 P32245 Melanocortin receptor 4 82.72% 95.38%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.66% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 80.91% 97.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.88% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.35% 97.09%
CHEMBL1871 P10275 Androgen Receptor 80.06% 96.43%

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 10665412
LOTUS LTS0020235
wikiData Q105159445