Epoxycembrene A

Details

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Internal ID 325f8c67-e6af-4ec5-b248-3413a504959a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4E,8E,12R,14S)-1,5,9-trimethyl-12-prop-1-en-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,8-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-15(2)18-12-11-17(4)9-6-8-16(3)10-7-13-20(5)19(14-18)21-20/h9-10,18-19H,1,6-8,11-14H2,2-5H3/b16-10+,17-9+/t18-,19+,20+/m1/s1
InChI Key KEOMEGAHKSPEBP-VWTPCSIPSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL510525

2D Structure

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2D Structure of Epoxycembrene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.8594 85.94%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5694 56.94%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.9530 95.30%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.5796 57.96%
P-glycoprotein inhibitior - 0.7780 77.80%
P-glycoprotein substrate - 0.8436 84.36%
CYP3A4 substrate + 0.5964 59.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7083 70.83%
CYP3A4 inhibition - 0.8093 80.93%
CYP2C9 inhibition + 0.7487 74.87%
CYP2C19 inhibition + 0.7837 78.37%
CYP2D6 inhibition - 0.9344 93.44%
CYP1A2 inhibition + 0.8734 87.34%
CYP2C8 inhibition + 0.4694 46.94%
CYP inhibitory promiscuity - 0.8513 85.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5314 53.14%
Eye corrosion - 0.8927 89.27%
Eye irritation - 0.7071 70.71%
Skin irritation + 0.5551 55.51%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8491 84.91%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5555 55.55%
skin sensitisation + 0.7567 75.67%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6222 62.22%
Acute Oral Toxicity (c) III 0.8236 82.36%
Estrogen receptor binding - 0.5734 57.34%
Androgen receptor binding - 0.6173 61.73%
Thyroid receptor binding - 0.5691 56.91%
Glucocorticoid receptor binding + 0.5650 56.50%
Aromatase binding - 0.5508 55.08%
PPAR gamma + 0.6823 68.23%
Honey bee toxicity - 0.8348 83.48%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9253 92.53%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.22% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.61% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 90.19% 89.63%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.97% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.51% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.30% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.69% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 85.94% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.07% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.46% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.90% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.52% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 10859180
LOTUS LTS0217187
wikiData Q105140103