(4S,4aR,8aS)-5,8a-dimethyl-4-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene

Details

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Internal ID 6bc52531-656f-4648-8ce3-df8ebbb5c459
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4S,4aR,8aS)-5,8a-dimethyl-4-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene
SMILES (Canonical) CC1=CCCC2(C1C(CCC2)C(=C)C)C
SMILES (Isomeric) CC1=CCC[C@]2([C@H]1[C@H](CCC2)C(=C)C)C
InChI InChI=1S/C15H24/c1-11(2)13-8-6-10-15(4)9-5-7-12(3)14(13)15/h7,13-14H,1,5-6,8-10H2,2-4H3/t13-,14-,15-/m1/s1
InChI Key OLYGAQAHPBFDGU-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 5.20
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,4aR,8aS)-5,8a-dimethyl-4-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene

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 + 0.8924 89.24%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.7525 75.25%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9354 93.54%
OATP1B3 inhibitior + 0.8939 89.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8897 88.97%
P-glycoprotein inhibitior - 0.9302 93.02%
P-glycoprotein substrate - 0.8484 84.84%
CYP3A4 substrate + 0.5110 51.10%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.7309 73.09%
CYP2C9 inhibition - 0.6961 69.61%
CYP2C19 inhibition - 0.5830 58.30%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition - 0.7962 79.62%
CYP2C8 inhibition - 0.6197 61.97%
CYP inhibitory promiscuity - 0.6408 64.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Warning 0.4497 44.97%
Eye corrosion - 0.9143 91.43%
Eye irritation + 0.9284 92.84%
Skin irritation - 0.5915 59.15%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.7423 74.23%
Human Ether-a-go-go-Related Gene inhibition + 0.7226 72.26%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5680 56.80%
skin sensitisation + 0.8210 82.10%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5169 51.69%
Acute Oral Toxicity (c) III 0.8468 84.68%
Estrogen receptor binding - 0.9315 93.15%
Androgen receptor binding - 0.6220 62.20%
Thyroid receptor binding - 0.7470 74.70%
Glucocorticoid receptor binding - 0.7958 79.58%
Aromatase binding - 0.8032 80.32%
PPAR gamma - 0.7815 78.15%
Honey bee toxicity - 0.9272 92.72%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5800 58.00%
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 96.43% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.19% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.43% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.74% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.30% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.48% 100.00%
CHEMBL1871 P10275 Androgen Receptor 83.29% 96.43%
CHEMBL1937 Q92769 Histone deacetylase 2 82.92% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.40% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.24% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.16% 95.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.96% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.42% 93.04%

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 21579271
LOTUS LTS0212811
wikiData Q105194194