(3R,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6-hexahydronaphthalene

Details

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Internal ID d134ae02-5015-4d39-8ed9-78903a739d0e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (3R,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6-hexahydronaphthalene
SMILES (Canonical) CC(=C)C1CCC2(C=CCC(=C)C2C1)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@]2(C=CCC(=C)[C@@H]2C1)C
InChI InChI=1S/C15H22/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h5,8,13-14H,1,3,6-7,9-10H2,2,4H3/t13-,14+,15-/m1/s1
InChI Key VPGIVOTXWKFIRP-QLFBSQMISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.8052 80.52%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.7746 77.46%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9038 90.38%
OATP1B3 inhibitior + 0.9095 90.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8371 83.71%
P-glycoprotein inhibitior - 0.9588 95.88%
P-glycoprotein substrate - 0.7584 75.84%
CYP3A4 substrate + 0.5513 55.13%
CYP2C9 substrate - 0.7853 78.53%
CYP2D6 substrate - 0.7460 74.60%
CYP3A4 inhibition - 0.7319 73.19%
CYP2C9 inhibition - 0.7746 77.46%
CYP2C19 inhibition - 0.6540 65.40%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.7761 77.61%
CYP2C8 inhibition - 0.8402 84.02%
CYP inhibitory promiscuity - 0.6460 64.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Warning 0.4462 44.62%
Eye corrosion - 0.8931 89.31%
Eye irritation - 0.6450 64.50%
Skin irritation - 0.6352 63.52%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.7907 79.07%
Human Ether-a-go-go-Related Gene inhibition + 0.6945 69.45%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6011 60.11%
skin sensitisation + 0.8646 86.46%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6219 62.19%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding - 0.8378 83.78%
Androgen receptor binding - 0.6340 63.40%
Thyroid receptor binding - 0.7410 74.10%
Glucocorticoid receptor binding - 0.7026 70.26%
Aromatase binding - 0.7182 71.82%
PPAR gamma - 0.7032 70.32%
Honey bee toxicity - 0.8734 87.34%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5200 52.00%
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 97.02% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.24% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.70% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.14% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.42% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.09% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 82.28% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.73% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.67% 92.94%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.48% 96.61%

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.
Callitris columellaris
Ongokea gore

Cross-Links

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PubChem 15381873
LOTUS LTS0122224
wikiData Q105142871