(4S,4aS,8aS)-8a-methyl-5-methylidene-4-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene

Details

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Internal ID 1d0d93ef-2da9-4c22-ac1c-320fde9f43ae
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4S,4aS,8aS)-8a-methyl-5-methylidene-4-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene
SMILES (Canonical) CC(=C)C1CCCC2(C1C(=C)CCC2)C
SMILES (Isomeric) CC(=C)[C@H]1CCC[C@@]2([C@@H]1C(=C)CCC2)C
InChI InChI=1S/C15H24/c1-11(2)13-8-6-10-15(4)9-5-7-12(3)14(13)15/h13-14H,1,3,5-10H2,2,4H3/t13-,14-,15-/m1/s1
InChI Key HRMKWYBXBKFOIS-RBSFLKMASA-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 5.40
Atomic LogP (AlogP) 4.73
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 (4S,4aS,8aS)-8a-methyl-5-methylidene-4-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene

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 + 0.8377 83.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.7746 77.46%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.8991 89.91%
OATP1B3 inhibitior + 0.9095 90.95%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9042 90.42%
P-glycoprotein inhibitior - 0.9031 90.31%
P-glycoprotein substrate - 0.8903 89.03%
CYP3A4 substrate - 0.5154 51.54%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
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 - 0.8099 80.99%
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 + 0.9515 95.15%
Skin irritation - 0.6352 63.52%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.8223 82.23%
Human Ether-a-go-go-Related Gene inhibition - 0.3644 36.44%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.8646 86.46%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5192 51.92%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding - 0.8632 86.32%
Androgen receptor binding - 0.5613 56.13%
Thyroid receptor binding - 0.7105 71.05%
Glucocorticoid receptor binding - 0.7683 76.83%
Aromatase binding - 0.7403 74.03%
PPAR gamma - 0.8075 80.75%
Honey bee toxicity - 0.9254 92.54%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5900 59.00%
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 95.89% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.66% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.54% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.20% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.91% 97.09%
CHEMBL1977 P11473 Vitamin D receptor 85.46% 99.43%
CHEMBL237 P41145 Kappa opioid receptor 84.83% 98.10%
CHEMBL2581 P07339 Cathepsin D 84.64% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.53% 100.00%
CHEMBL259 P32245 Melanocortin receptor 4 83.18% 95.38%
CHEMBL233 P35372 Mu opioid receptor 80.73% 97.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.09% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.08% 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.
Saccogyna viticulosa

Cross-Links

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PubChem 12310323
LOTUS LTS0108865
wikiData Q104375421