(3aR)-2,2,8-Trimethyl-4-methylene-2,3,3aalpha,4,5,6,9,9aalpha-octahydro-1H-cyclopentacyclooctene

Details

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Internal ID 2ae31e2f-5635-4419-b350-76fa4e88488a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3aR,5Z,9aR)-2,2,5-trimethyl-9-methylidene-3,3a,4,7,8,9a-hexahydro-1H-cyclopenta[8]annulene
SMILES (Canonical) CC1=CCCC(=C)C2CC(CC2C1)(C)C
SMILES (Isomeric) C/C/1=C/CCC(=C)[C@@H]2CC(C[C@@H]2C1)(C)C
InChI InChI=1S/C15H24/c1-11-6-5-7-12(2)14-10-15(3,4)9-13(14)8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6-/t13-,14-/m0/s1
InChI Key JRCVPJOABWZGQV-BJLYVFBQSA-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 4.40
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
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 (3aR)-2,2,8-Trimethyl-4-methylene-2,3,3aalpha,4,5,6,9,9aalpha-octahydro-1H-cyclopentacyclooctene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.8899 88.99%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7009 70.09%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9313 93.13%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6695 66.95%
P-glycoprotein inhibitior - 0.9237 92.37%
P-glycoprotein substrate - 0.8947 89.47%
CYP3A4 substrate - 0.5551 55.51%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9048 90.48%
CYP2C9 inhibition - 0.7194 71.94%
CYP2C19 inhibition - 0.6708 67.08%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.7339 73.39%
CYP2C8 inhibition - 0.7702 77.02%
CYP inhibitory promiscuity - 0.7940 79.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion - 0.8547 85.47%
Eye irritation + 0.7858 78.58%
Skin irritation + 0.5845 58.45%
Skin corrosion - 0.9814 98.14%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3652 36.52%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8626 86.26%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5751 57.51%
Acute Oral Toxicity (c) III 0.8226 82.26%
Estrogen receptor binding - 0.9281 92.81%
Androgen receptor binding - 0.6111 61.11%
Thyroid receptor binding - 0.8326 83.26%
Glucocorticoid receptor binding - 0.7652 76.52%
Aromatase binding - 0.7303 73.03%
PPAR gamma - 0.8465 84.65%
Honey bee toxicity - 0.8471 84.71%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7100 71.00%
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 95.91% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.41% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.03% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.79% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.55% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.27% 86.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.57% 95.89%

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.
Lippia integrifolia

Cross-Links

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PubChem 15519994
LOTUS LTS0048206
wikiData Q105133826