(+)-6,11-Epoxyeudesmane

Details

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Internal ID ed617788-f779-42da-afb2-7e89da041daf
Taxonomy Organoheterocyclic compounds > Oxetanes
IUPAC Name (2aR,4aS,8R,8aR,8bS)-2,2,4a,8-tetramethyl-3,4,5,6,7,8,8a,8b-octahydro-2aH-naphtho[1,2-b]oxete
SMILES (Canonical) CC1CCCC2(C1C3C(CC2)C(O3)(C)C)C
SMILES (Isomeric) C[C@@H]1CCC[C@@]2([C@@H]1[C@H]3[C@@H](CC2)C(O3)(C)C)C
InChI InChI=1S/C15H26O/c1-10-6-5-8-15(4)9-7-11-13(12(10)15)16-14(11,2)3/h10-13H,5-9H2,1-4H3/t10-,11-,12+,13-,15+/m1/s1
InChI Key CBZJHBRKOJFYDB-VVSAWPALSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-6,11-Epoxyeudesmane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8679 86.79%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.5467 54.67%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9140 91.40%
P-glycoprotein inhibitior - 0.8841 88.41%
P-glycoprotein substrate - 0.9340 93.40%
CYP3A4 substrate + 0.5989 59.89%
CYP2C9 substrate - 0.8017 80.17%
CYP2D6 substrate - 0.7026 70.26%
CYP3A4 inhibition - 0.9404 94.04%
CYP2C9 inhibition - 0.6431 64.31%
CYP2C19 inhibition - 0.5065 50.65%
CYP2D6 inhibition - 0.9401 94.01%
CYP1A2 inhibition - 0.6770 67.70%
CYP2C8 inhibition - 0.7784 77.84%
CYP inhibitory promiscuity - 0.8810 88.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5397 53.97%
Eye corrosion - 0.8762 87.62%
Eye irritation - 0.5890 58.90%
Skin irritation - 0.6657 66.57%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6904 69.04%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.5286 52.86%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4815 48.15%
Acute Oral Toxicity (c) III 0.7379 73.79%
Estrogen receptor binding - 0.5468 54.68%
Androgen receptor binding + 0.6017 60.17%
Thyroid receptor binding + 0.6087 60.87%
Glucocorticoid receptor binding - 0.6253 62.53%
Aromatase binding - 0.7155 71.55%
PPAR gamma - 0.7395 73.95%
Honey bee toxicity - 0.7171 71.71%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9474 94.74%

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 89.38% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.12% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.83% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.30% 92.94%
CHEMBL4040 P28482 MAP kinase ERK2 88.19% 83.82%
CHEMBL5203 P33316 dUTP pyrophosphatase 87.81% 99.18%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.47% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.36% 96.61%
CHEMBL259 P32245 Melanocortin receptor 4 85.08% 95.38%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.78% 95.58%
CHEMBL233 P35372 Mu opioid receptor 83.36% 97.93%
CHEMBL237 P41145 Kappa opioid receptor 83.15% 98.10%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.31% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.62% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 80.27% 97.79%
CHEMBL1871 P10275 Androgen Receptor 80.17% 96.43%

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.
Saccobasis polita

Cross-Links

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PubChem 21576506
LOTUS LTS0255982
wikiData Q104953005