1-Methoxyadamantane

Details

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Internal ID 05350ccf-34ed-48d1-9343-87250aae0d2e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-methoxyadamantane
SMILES (Canonical) COC12CC3CC(C1)CC(C3)C2
SMILES (Isomeric) COC12CC3CC(C1)CC(C3)C2
InChI InChI=1S/C11H18O/c1-12-11-5-8-2-9(6-11)4-10(3-8)7-11/h8-10H,2-7H2,1H3
InChI Key VLBPHZFRABGLFH-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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6221-74-5
1-Adamantyl methyl ether #
SCHEMBL727714
SCHEMBL10584195
VLBPHZFRABGLFH-UHFFFAOYSA-N
AKOS040766678

2D Structure

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2D Structure of 1-Methoxyadamantane

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 + 0.7425 74.25%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4856 48.56%
OATP2B1 inhibitior - 0.8739 87.39%
OATP1B1 inhibitior + 0.9748 97.48%
OATP1B3 inhibitior + 0.9757 97.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9459 94.59%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate - 0.5818 58.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6826 68.26%
CYP3A4 inhibition - 0.8983 89.83%
CYP2C9 inhibition - 0.7902 79.02%
CYP2C19 inhibition - 0.6709 67.09%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.6429 64.29%
CYP2C8 inhibition - 0.9386 93.86%
CYP inhibitory promiscuity - 0.8778 87.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7628 76.28%
Carcinogenicity (trinary) Non-required 0.5099 50.99%
Eye corrosion - 0.8848 88.48%
Eye irritation + 0.9845 98.45%
Skin irritation - 0.5492 54.92%
Skin corrosion - 0.9214 92.14%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6806 68.06%
Micronuclear - 0.8951 89.51%
Hepatotoxicity - 0.6489 64.89%
skin sensitisation + 0.5369 53.69%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5820 58.20%
Acute Oral Toxicity (c) III 0.7694 76.94%
Estrogen receptor binding - 0.8879 88.79%
Androgen receptor binding - 0.7955 79.55%
Thyroid receptor binding - 0.7835 78.35%
Glucocorticoid receptor binding - 0.8866 88.66%
Aromatase binding - 0.8293 82.93%
PPAR gamma - 0.8221 82.21%
Honey bee toxicity - 0.6502 65.02%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.4599 45.99%

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 92.45% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.14% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.09% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.50% 91.11%
CHEMBL1871 P10275 Androgen Receptor 84.01% 96.43%
CHEMBL1968 P07099 Epoxide hydrolase 1 82.95% 98.57%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.95% 97.14%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.82% 85.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.15% 94.45%

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.
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

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PubChem 584854
NPASS NPC109966
LOTUS LTS0147133
wikiData Q105288250