Pethybrene

Details

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Internal ID f797e9f2-72e0-4965-b52c-6b3d523ddc00
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Angular triquinanes
IUPAC Name (1S,2R,5S,8S)-2,5,8-trimethyl-7-methylidenetricyclo[6.3.0.01,5]undecane
SMILES (Canonical) CC1CCC2(C13CCCC3(C(=C)C2)C)C
SMILES (Isomeric) C[C@@H]1CC[C@@]2([C@]13CCC[C@]3(C(=C)C2)C)C
InChI InChI=1S/C15H24/c1-11-6-9-13(3)10-12(2)14(4)7-5-8-15(11,13)14/h11H,2,5-10H2,1,3-4H3/t11-,13+,14+,15+/m1/s1
InChI Key BPSJFUIWVOWJNO-UNQGMJICSA-N
Popularity 1 reference 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 5.10
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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BPSJFUIWVOWJNO-UNQGMJICSA-N
(1S,2R,5S,8S)-2,5,8-trimethyl-7-methylidenetricyclo[6.3.0.01,5]undecane

2D Structure

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2D Structure of Pethybrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8154 81.54%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.7975 79.75%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.9128 91.28%
OATP1B3 inhibitior + 0.8834 88.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8253 82.53%
P-glycoprotein inhibitior - 0.9394 93.94%
P-glycoprotein substrate - 0.8877 88.77%
CYP3A4 substrate + 0.5142 51.42%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7431 74.31%
CYP3A4 inhibition - 0.8702 87.02%
CYP2C9 inhibition - 0.8013 80.13%
CYP2C19 inhibition - 0.7460 74.60%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition - 0.7020 70.20%
CYP2C8 inhibition - 0.9005 90.05%
CYP inhibitory promiscuity - 0.7490 74.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.4527 45.27%
Eye corrosion - 0.9072 90.72%
Eye irritation + 0.9105 91.05%
Skin irritation + 0.5387 53.87%
Skin corrosion - 0.9792 97.92%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6724 67.24%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5594 55.94%
skin sensitisation + 0.8364 83.64%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6153 61.53%
Acute Oral Toxicity (c) III 0.7802 78.02%
Estrogen receptor binding - 0.8941 89.41%
Androgen receptor binding + 0.5472 54.72%
Thyroid receptor binding - 0.8135 81.35%
Glucocorticoid receptor binding - 0.8578 85.78%
Aromatase binding - 0.7228 72.28%
PPAR gamma - 0.8258 82.58%
Honey bee toxicity - 0.9111 91.11%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7200 72.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.73% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.32% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.66% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.07% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.66% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.02% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.94% 82.69%
CHEMBL2581 P07339 Cathepsin D 81.21% 98.95%
CHEMBL1902 P62942 FK506-binding protein 1A 80.98% 97.05%
CHEMBL1937 Q92769 Histone deacetylase 2 80.26% 94.75%

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.
Petasites hybridus

Cross-Links

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PubChem 11052748
LOTUS LTS0205494
wikiData Q104943755