(1R)-7-methoxy-1-methyl-1,2,3,4-tetrahydronaphthalene

Details

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Internal ID 2ee67508-84e8-482c-8c21-8971fa7d4a4f
Taxonomy Benzenoids > Tetralins
IUPAC Name (1R)-7-methoxy-1-methyl-1,2,3,4-tetrahydronaphthalene
SMILES (Canonical) CC1CCCC2=C1C=C(C=C2)OC
SMILES (Isomeric) C[C@@H]1CCCC2=C1C=C(C=C2)OC
InChI InChI=1S/C12H16O/c1-9-4-3-5-10-6-7-11(13-2)8-12(9)10/h6-9H,3-5H2,1-2H3/t9-/m1/s1
InChI Key KSWPMXHTZCMXBJ-SECBINFHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O
Molecular Weight 176.25 g/mol
Exact Mass 176.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 1
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)-7-methoxy-1-methyl-1,2,3,4-tetrahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9197 91.97%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5554 55.54%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9202 92.02%
OATP1B3 inhibitior + 0.9728 97.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7888 78.88%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.8441 84.41%
CYP3A4 substrate - 0.5283 52.83%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.5289 52.89%
CYP3A4 inhibition - 0.9426 94.26%
CYP2C9 inhibition - 0.8755 87.55%
CYP2C19 inhibition - 0.7883 78.83%
CYP2D6 inhibition - 0.8712 87.12%
CYP1A2 inhibition + 0.8902 89.02%
CYP2C8 inhibition - 0.8903 89.03%
CYP inhibitory promiscuity - 0.6944 69.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7342 73.42%
Carcinogenicity (trinary) Non-required 0.5291 52.91%
Eye corrosion - 0.8149 81.49%
Eye irritation - 0.5532 55.32%
Skin irritation - 0.5328 53.28%
Skin corrosion - 0.6692 66.92%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4522 45.22%
Micronuclear - 0.9041 90.41%
Hepatotoxicity - 0.6665 66.65%
skin sensitisation + 0.5312 53.12%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.8274 82.74%
Acute Oral Toxicity (c) III 0.6891 68.91%
Estrogen receptor binding - 0.9394 93.94%
Androgen receptor binding - 0.7108 71.08%
Thyroid receptor binding - 0.6779 67.79%
Glucocorticoid receptor binding - 0.8085 80.85%
Aromatase binding - 0.8981 89.81%
PPAR gamma - 0.8842 88.42%
Honey bee toxicity - 0.9569 95.69%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9735 97.35%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.49% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.63% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.96% 93.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.36% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.08% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 89.91% 91.49%
CHEMBL5203 P33316 dUTP pyrophosphatase 88.58% 99.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL4581 P52732 Kinesin-like protein 1 88.13% 93.18%
CHEMBL1907 P15144 Aminopeptidase N 87.28% 93.31%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.12% 92.62%
CHEMBL2581 P07339 Cathepsin D 83.94% 98.95%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.68% 100.00%
CHEMBL4208 P20618 Proteasome component C5 83.56% 90.00%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 83.31% 91.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.12% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 82.70% 95.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.81% 99.17%
CHEMBL3438 Q05513 Protein kinase C zeta 81.49% 88.48%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.38% 91.07%

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.
Grindelia hirsutula

Cross-Links

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PubChem 59377464
LOTUS LTS0256022
wikiData Q105145619