8-Hydroperoxy-3,3-dimethyl-7,11-dimethylidenecycloundecene

Details

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Internal ID 713a9220-615b-44cd-8297-39bdf9d0fa6c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 8-hydroperoxy-3,3-dimethyl-7,11-dimethylidenecycloundecene
SMILES (Canonical) CC1(CCCC(=C)C(CCC(=C)C=C1)OO)C
SMILES (Isomeric) CC1(CCCC(=C)C(CCC(=C)C=C1)OO)C
InChI InChI=1S/C15H24O2/c1-12-7-8-14(17-16)13(2)6-5-10-15(3,4)11-9-12/h9,11,14,16H,1-2,5-8,10H2,3-4H3
InChI Key NVVYRRHQKSVSBM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Hydroperoxy-3,3-dimethyl-7,11-dimethylidenecycloundecene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.8531 85.31%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6724 67.24%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.8959 89.59%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8756 87.56%
P-glycoprotein inhibitior - 0.9197 91.97%
P-glycoprotein substrate - 0.9006 90.06%
CYP3A4 substrate + 0.5419 54.19%
CYP2C9 substrate - 0.6108 61.08%
CYP2D6 substrate - 0.7800 78.00%
CYP3A4 inhibition - 0.6767 67.67%
CYP2C9 inhibition - 0.7858 78.58%
CYP2C19 inhibition - 0.6440 64.40%
CYP2D6 inhibition - 0.9203 92.03%
CYP1A2 inhibition - 0.6644 66.44%
CYP2C8 inhibition - 0.7039 70.39%
CYP inhibitory promiscuity - 0.8067 80.67%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6671 66.71%
Carcinogenicity (trinary) Non-required 0.5520 55.20%
Eye corrosion - 0.9148 91.48%
Eye irritation - 0.5120 51.20%
Skin irritation - 0.5421 54.21%
Skin corrosion - 0.8979 89.79%
Ames mutagenesis - 0.7424 74.24%
Human Ether-a-go-go-Related Gene inhibition + 0.7081 70.81%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5484 54.84%
skin sensitisation + 0.6246 62.46%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6714 67.14%
Acute Oral Toxicity (c) III 0.6875 68.75%
Estrogen receptor binding - 0.6811 68.11%
Androgen receptor binding - 0.7347 73.47%
Thyroid receptor binding - 0.5238 52.38%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.7408 74.08%
PPAR gamma - 0.5364 53.64%
Honey bee toxicity - 0.8984 89.84%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9842 98.42%

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 96.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.92% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.66% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.96% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.93% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.23% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.27% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 81.92% 91.49%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.25% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.00% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.55% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 80.38% 83.82%

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.
Artemisia douglasiana
Eurycoma harmandiana
Eurycoma longifolia

Cross-Links

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PubChem 163081882
LOTUS LTS0133957
wikiData Q27134546