(1S,4aR)-1,4a-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene

Details

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Internal ID 5f35c980-2c30-4de1-96c8-7b206e1a9485
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name (1S,4aR)-1,4a-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene
SMILES (Canonical) CC1CCCC2(C1=CCCC2)C
SMILES (Isomeric) C[C@H]1CCC[C@@]2(C1=CCCC2)C
InChI InChI=1S/C12H20/c1-10-6-5-9-12(2)8-4-3-7-11(10)12/h7,10H,3-6,8-9H2,1-2H3/t10-,12+/m0/s1
InChI Key QPKYDOXXVXJLPX-CMPLNLGQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H20
Molecular Weight 164.29 g/mol
Exact Mass 164.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aR)-1,4a-dimethyl-2,3,4,5,6,7-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 + 0.9944 99.44%
Caco-2 + 0.9173 91.73%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.7274 72.74%
OATP2B1 inhibitior - 0.8396 83.96%
OATP1B1 inhibitior + 0.9542 95.42%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8257 82.57%
P-glycoprotein inhibitior - 0.9718 97.18%
P-glycoprotein substrate - 0.9531 95.31%
CYP3A4 substrate - 0.5725 57.25%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8292 82.92%
CYP2C9 inhibition - 0.7519 75.19%
CYP2C19 inhibition - 0.6855 68.55%
CYP2D6 inhibition - 0.9081 90.81%
CYP1A2 inhibition - 0.8077 80.77%
CYP2C8 inhibition - 0.8692 86.92%
CYP inhibitory promiscuity - 0.6080 60.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.4396 43.96%
Eye corrosion - 0.9218 92.18%
Eye irritation + 0.8058 80.58%
Skin irritation - 0.6703 67.03%
Skin corrosion - 0.9493 94.93%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5479 54.79%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5766 57.66%
skin sensitisation + 0.8551 85.51%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7042 70.42%
Acute Oral Toxicity (c) III 0.7454 74.54%
Estrogen receptor binding - 0.9468 94.68%
Androgen receptor binding - 0.6466 64.66%
Thyroid receptor binding - 0.8271 82.71%
Glucocorticoid receptor binding - 0.8834 88.34%
Aromatase binding - 0.7374 73.74%
PPAR gamma - 0.8814 88.14%
Honey bee toxicity - 0.9683 96.83%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7800 78.00%
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 93.86% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.47% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.23% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.98% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.48% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.79% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.31% 82.69%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.52% 86.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.32% 90.17%

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.
Lophocolea bidentata

Cross-Links

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PubChem 15959550
LOTUS LTS0020553
wikiData Q105225450