(-)-Bicycloelemene

Details

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Internal ID 30ef413a-c7d8-40b0-9479-3648a7559b8f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Elemane sesquiterpenoids
IUPAC Name (1R,2R,3R,6R)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-7-15(6)9-8-11-13(14(11,4)5)12(15)10(2)3/h7,11-13H,1-2,8-9H2,3-6H3/t11-,12+,13-,15+/m1/s1
InChI Key LKQMMFFQYMYQOJ-COMQUAJESA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.44
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(-)-Bicycloelemene
CHEBI:172935
RefChem:1049088
32531-56-9

2D Structure

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2D Structure of (-)-Bicycloelemene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.5398 53.98%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7390 73.90%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9197 91.97%
OATP1B3 inhibitior + 0.7973 79.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9769 97.69%
P-glycoprotein inhibitior - 0.9179 91.79%
P-glycoprotein substrate - 0.8939 89.39%
CYP3A4 substrate + 0.5337 53.37%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.8637 86.37%
CYP2C9 inhibition - 0.8281 82.81%
CYP2C19 inhibition - 0.7376 73.76%
CYP2D6 inhibition - 0.9157 91.57%
CYP1A2 inhibition - 0.7340 73.40%
CYP2C8 inhibition - 0.7947 79.47%
CYP inhibitory promiscuity - 0.7344 73.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.4773 47.73%
Eye corrosion - 0.9125 91.25%
Eye irritation + 0.6670 66.70%
Skin irritation + 0.6909 69.09%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4400 44.00%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7002 70.02%
skin sensitisation + 0.8357 83.57%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5035 50.35%
Nephrotoxicity + 0.5971 59.71%
Acute Oral Toxicity (c) III 0.8709 87.09%
Estrogen receptor binding - 0.7501 75.01%
Androgen receptor binding + 0.5599 55.99%
Thyroid receptor binding - 0.6156 61.56%
Glucocorticoid receptor binding - 0.7540 75.40%
Aromatase binding - 0.7791 77.91%
PPAR gamma - 0.7426 74.26%
Honey bee toxicity - 0.6017 60.17%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9955 99.55%

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 92.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.98% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.80% 97.25%
CHEMBL233 P35372 Mu opioid receptor 89.36% 97.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.73% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.69% 92.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.23% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 81.93% 94.75%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.83% 95.50%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.72% 91.03%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.04% 89.05%
CHEMBL221 P23219 Cyclooxygenase-1 80.66% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.62% 97.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.06% 82.05%

Cross-Links

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PubChem 101973934
NPASS NPC142104
LOTUS LTS0204053
wikiData Q77373777