(3R,4aR,8aR)-5,8a-dimethyl-3-propan-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene

Details

Top
Internal ID cc3085f8-bc59-4d19-8ff0-70e455d17b06
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (3R,4aR,8aR)-5,8a-dimethyl-3-propan-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene
SMILES (Canonical) CC1=CCCC2(C1CC(CC2)C(C)C)C
SMILES (Isomeric) CC1=CCC[C@@]2([C@H]1C[C@@H](CC2)C(C)C)C
InChI InChI=1S/C15H26/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h6,11,13-14H,5,7-10H2,1-4H3/t13-,14+,15+/m1/s1
InChI Key VPQBJIRQUUEAFC-ILXRZTDVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.81
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3R,4aR,8aR)-5,8a-dimethyl-3-propan-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8145 81.45%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6591 65.91%
OATP2B1 inhibitior - 0.8459 84.59%
OATP1B1 inhibitior + 0.9431 94.31%
OATP1B3 inhibitior + 0.9060 90.60%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7440 74.40%
P-glycoprotein inhibitior - 0.9372 93.72%
P-glycoprotein substrate - 0.8231 82.31%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.8496 84.96%
CYP2C9 inhibition - 0.7310 73.10%
CYP2C19 inhibition - 0.5883 58.83%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.8599 85.99%
CYP2C8 inhibition - 0.8340 83.40%
CYP inhibitory promiscuity - 0.6021 60.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4653 46.53%
Eye corrosion - 0.9347 93.47%
Eye irritation - 0.5257 52.57%
Skin irritation - 0.5967 59.67%
Skin corrosion - 0.9487 94.87%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4647 46.47%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6162 61.62%
skin sensitisation + 0.8700 87.00%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5946 59.46%
Acute Oral Toxicity (c) III 0.7313 73.13%
Estrogen receptor binding - 0.9479 94.79%
Androgen receptor binding - 0.7076 70.76%
Thyroid receptor binding - 0.7259 72.59%
Glucocorticoid receptor binding - 0.7026 70.26%
Aromatase binding - 0.8878 88.78%
PPAR gamma - 0.8495 84.95%
Honey bee toxicity - 0.8321 83.21%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 97.65% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.80% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.96% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.05% 97.23%
CHEMBL221 P23219 Cyclooxygenase-1 85.30% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.01% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.86% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.39% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.86% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.67% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.45% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 80.52% 97.79%

Plants that contains it

Top
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.
Abies firma

Cross-Links

Top
PubChem 140799050
LOTUS LTS0057365
wikiData Q105290923