epsilon-Bulgarene

Details

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Internal ID 941f6bc9-0126-4e11-8dd1-daf920bbb84d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4aS,8aR)-4,7-dimethylidene-1-propan-2-yl-1,2,3,4a,5,6,8,8a-octahydronaphthalene
SMILES (Canonical) CC(C)C1CCC(=C)C2C1CC(=C)CC2
SMILES (Isomeric) CC(C)[C@@H]1CCC(=C)[C@@H]2[C@@H]1CC(=C)CC2
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h10,13-15H,3-9H2,1-2H3/t13-,14+,15+/m0/s1
InChI Key NOLWRMQDWRAODO-RRFJBIMHSA-N
Popularity 0 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 4.50
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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15890-31-0
(1S,4As,8aR)-4,7-dimethylidene-1-propan-2-yl-1,2,3,4a,5,6,8,8a-octahydronaphthalene

2D Structure

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2D Structure of epsilon-Bulgarene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.8421 84.21%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7167 71.67%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior + 0.9222 92.22%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9256 92.56%
P-glycoprotein inhibitior - 0.9203 92.03%
P-glycoprotein substrate - 0.8118 81.18%
CYP3A4 substrate - 0.5858 58.58%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.9067 90.67%
CYP2C9 inhibition - 0.8079 80.79%
CYP2C19 inhibition - 0.7035 70.35%
CYP2D6 inhibition - 0.9075 90.75%
CYP1A2 inhibition - 0.6554 65.54%
CYP2C8 inhibition - 0.9408 94.08%
CYP inhibitory promiscuity - 0.5419 54.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4826 48.26%
Eye corrosion - 0.6999 69.99%
Eye irritation + 0.9451 94.51%
Skin irritation - 0.5689 56.89%
Skin corrosion - 0.9355 93.55%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4463 44.63%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.8947 89.47%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6065 60.65%
Acute Oral Toxicity (c) III 0.6707 67.07%
Estrogen receptor binding - 0.7877 78.77%
Androgen receptor binding - 0.4860 48.60%
Thyroid receptor binding - 0.6862 68.62%
Glucocorticoid receptor binding - 0.5586 55.86%
Aromatase binding - 0.7857 78.57%
PPAR gamma - 0.7826 78.26%
Honey bee toxicity - 0.8736 87.36%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL2581 P07339 Cathepsin D 89.54% 98.95%
CHEMBL1871 P10275 Androgen Receptor 85.47% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.93% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.86% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.24% 100.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.88% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.80% 95.89%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.33% 97.23%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.84% 90.24%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.54% 90.71%

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.
Larix sibirica
Mentha × piperita

Cross-Links

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PubChem 12302128
NPASS NPC176062
LOTUS LTS0223331
wikiData Q104253316