(1R,4R,4aS,8aS)-1,6-dimethyl-4-prop-1-en-2-yl-1,2,3,4,4a,5,8,8a-octahydronaphthalene

Details

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Internal ID 33835783-0b02-4aa9-a4b7-b072dcc6e2a9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4R,4aS,8aS)-1,6-dimethyl-4-prop-1-en-2-yl-1,2,3,4,4a,5,8,8a-octahydronaphthalene
SMILES (Canonical) CC1CCC(C2C1CC=C(C2)C)C(=C)C
SMILES (Isomeric) C[C@@H]1CC[C@H]([C@@H]2[C@H]1CC=C(C2)C)C(=C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5,12-15H,1,6-9H2,2-4H3/t12-,13+,14+,15-/m1/s1
InChI Key YJEJSDONBOFVNH-CBBWQLFWSA-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 5.00
Atomic LogP (AlogP) 4.58
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 (1R,4R,4aS,8aS)-1,6-dimethyl-4-prop-1-en-2-yl-1,2,3,4,4a,5,8,8a-octahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8979 89.79%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.6800 68.00%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9623 96.23%
OATP1B3 inhibitior + 0.9193 91.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9126 91.26%
P-glycoprotein inhibitior - 0.9432 94.32%
P-glycoprotein substrate - 0.7230 72.30%
CYP3A4 substrate - 0.5373 53.73%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.8211 82.11%
CYP2C9 inhibition - 0.7804 78.04%
CYP2C19 inhibition - 0.6625 66.25%
CYP2D6 inhibition - 0.9200 92.00%
CYP1A2 inhibition - 0.6438 64.38%
CYP2C8 inhibition - 0.7962 79.62%
CYP inhibitory promiscuity - 0.5873 58.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Warning 0.4334 43.34%
Eye corrosion - 0.8123 81.23%
Eye irritation + 0.8614 86.14%
Skin irritation - 0.5209 52.09%
Skin corrosion - 0.9291 92.91%
Ames mutagenesis - 0.8154 81.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4051 40.51%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7793 77.93%
skin sensitisation + 0.8566 85.66%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8314 83.14%
Estrogen receptor binding - 0.8978 89.78%
Androgen receptor binding - 0.5826 58.26%
Thyroid receptor binding - 0.7067 70.67%
Glucocorticoid receptor binding - 0.7301 73.01%
Aromatase binding - 0.7873 78.73%
PPAR gamma - 0.7483 74.83%
Honey bee toxicity - 0.8704 87.04%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.67% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.03% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.89% 93.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.57% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.76% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.34% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.13% 97.25%
CHEMBL2581 P07339 Cathepsin D 83.92% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.88% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.19% 97.21%

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.
Chiloscyphus polyanthos var. rivularis
Conocarpus erectus
Fabiana imbricata
Lupinus pilosus
Magnolia fraseri
Rubus occidentalis

Cross-Links

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PubChem 10899738
NPASS NPC213312
LOTUS LTS0134073
wikiData Q105349207