6,6-Dimethyl-2-methylidenebicyclo(3.1.1)heptane-3-peroxol

Details

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Internal ID 69819bdf-5ccf-48e6-be99-99992703c6b6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 3-hydroperoxy-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-6-8-4-7(10(8,2)3)5-9(6)12-11/h7-9,11H,1,4-5H2,2-3H3
InChI Key UQHVOBUXTHVSBI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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DTXSID10550485
6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptane-3-peroxol

2D Structure

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2D Structure of 6,6-Dimethyl-2-methylidenebicyclo(3.1.1)heptane-3-peroxol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 - 0.5749 57.49%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6821 68.21%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9158 91.58%
OATP1B3 inhibitior + 0.9347 93.47%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9561 95.61%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.9136 91.36%
CYP3A4 substrate - 0.5101 51.01%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7655 76.55%
CYP3A4 inhibition - 0.6602 66.02%
CYP2C9 inhibition - 0.7383 73.83%
CYP2C19 inhibition + 0.5406 54.06%
CYP2D6 inhibition - 0.9049 90.49%
CYP1A2 inhibition - 0.8113 81.13%
CYP2C8 inhibition - 0.9062 90.62%
CYP inhibitory promiscuity - 0.6757 67.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7256 72.56%
Carcinogenicity (trinary) Non-required 0.5703 57.03%
Eye corrosion - 0.9323 93.23%
Eye irritation + 0.9246 92.46%
Skin irritation - 0.6705 67.05%
Skin corrosion - 0.8393 83.93%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5053 50.53%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.6335 63.35%
skin sensitisation + 0.6279 62.79%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5574 55.74%
Acute Oral Toxicity (c) III 0.6815 68.15%
Estrogen receptor binding - 0.7908 79.08%
Androgen receptor binding - 0.7306 73.06%
Thyroid receptor binding - 0.7110 71.10%
Glucocorticoid receptor binding - 0.7430 74.30%
Aromatase binding - 0.8021 80.21%
PPAR gamma - 0.7898 78.98%
Honey bee toxicity - 0.7388 73.88%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9811 98.11%

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 92.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.52% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 87.96% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.24% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.78% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.80% 97.25%

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.
Achillea filipendulina
Chamaemelum nobile

Cross-Links

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PubChem 13819203
LOTUS LTS0223953
wikiData Q82429871