1-Methyl-3-propan-2-yloxycyclohexane

Details

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Internal ID 5b89f96f-2f4a-4784-ab23-37809fa1cf16
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-methyl-3-propan-2-yloxycyclohexane
SMILES (Canonical) CC1CCCC(C1)OC(C)C
SMILES (Isomeric) CC1CCCC(C1)OC(C)C
InChI InChI=1S/C10H20O/c1-8(2)11-10-6-4-5-9(3)7-10/h8-10H,4-7H2,1-3H3
InChI Key LXJQGSJHOKQAPO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-3-propan-2-yloxycyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9266 92.66%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6516 65.16%
OATP2B1 inhibitior - 0.8446 84.46%
OATP1B1 inhibitior + 0.9470 94.70%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9549 95.49%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.8783 87.83%
CYP3A4 substrate - 0.6132 61.32%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7078 70.78%
CYP3A4 inhibition - 0.9664 96.64%
CYP2C9 inhibition - 0.8996 89.96%
CYP2C19 inhibition - 0.8762 87.62%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.8095 80.95%
CYP2C8 inhibition - 0.9507 95.07%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6440 64.40%
Eye corrosion + 0.9164 91.64%
Eye irritation + 0.9572 95.72%
Skin irritation + 0.7503 75.03%
Skin corrosion - 0.9019 90.19%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6799 67.99%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5218 52.18%
skin sensitisation + 0.8066 80.66%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8275 82.75%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5584 55.84%
Acute Oral Toxicity (c) III 0.8002 80.02%
Estrogen receptor binding - 0.9310 93.10%
Androgen receptor binding - 0.9193 91.93%
Thyroid receptor binding - 0.7199 71.99%
Glucocorticoid receptor binding - 0.8664 86.64%
Aromatase binding - 0.8164 81.64%
PPAR gamma - 0.9044 90.44%
Honey bee toxicity - 0.8204 82.04%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8909 89.09%

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 95.79% 97.25%
CHEMBL5203 P33316 dUTP pyrophosphatase 91.20% 99.18%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.62% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.20% 96.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.96% 97.23%
CHEMBL206 P03372 Estrogen receptor alpha 85.68% 97.64%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.63% 95.27%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.02% 96.47%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.89% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 81.26% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.22% 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.
Alpinia oxyphylla
Phedimus kamtschaticus
Punica granatum
Sedum sarmentosum

Cross-Links

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PubChem 5319690
NPASS NPC91980