2-Methylidene-5-(prop-1-EN-2-YL)cyclohexane-1-peroxol

Details

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Internal ID a95737c6-cdf7-492c-bd63-941a475a2b33
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-hydroperoxy-1-methylidene-4-prop-1-en-2-ylcyclohexane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-7(2)9-5-4-8(3)10(6-9)12-11/h9-11H,1,3-6H2,2H3
InChI Key CSOZFPOODGAASP-UHFFFAOYSA-N
Popularity 1 reference 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 2.30
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CSOZFPOODGAASP-UHFFFAOYSA-N
DTXSID401017494
(Z)-p-mentha-1,8-dien-2-hydroperoxide
5-Isopropenyl-2-methylenecyclohexyl hydroperoxide #
77026-83-6

2D Structure

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2D Structure of 2-Methylidene-5-(prop-1-EN-2-YL)cyclohexane-1-peroxol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 - 0.6186 61.86%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7438 74.38%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9466 94.66%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9782 97.82%
P-glycoprotein inhibitior - 0.9750 97.50%
P-glycoprotein substrate - 0.8411 84.11%
CYP3A4 substrate - 0.5708 57.08%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7344 73.44%
CYP3A4 inhibition - 0.8306 83.06%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.7348 73.48%
CYP2D6 inhibition - 0.9071 90.71%
CYP1A2 inhibition - 0.7752 77.52%
CYP2C8 inhibition - 0.8770 87.70%
CYP inhibitory promiscuity - 0.7611 76.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6971 69.71%
Carcinogenicity (trinary) Non-required 0.5796 57.96%
Eye corrosion - 0.7723 77.23%
Eye irritation + 0.8276 82.76%
Skin irritation - 0.5233 52.33%
Skin corrosion - 0.8919 89.19%
Ames mutagenesis - 0.7791 77.91%
Human Ether-a-go-go-Related Gene inhibition - 0.4747 47.47%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.6098 60.98%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5065 50.65%
Acute Oral Toxicity (c) III 0.7408 74.08%
Estrogen receptor binding - 0.8410 84.10%
Androgen receptor binding - 0.8296 82.96%
Thyroid receptor binding - 0.7414 74.14%
Glucocorticoid receptor binding - 0.8199 81.99%
Aromatase binding - 0.8254 82.54%
PPAR gamma - 0.7904 79.04%
Honey bee toxicity - 0.8285 82.85%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9651 96.51%

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 94.35% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.91% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.53% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.50% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.64% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.76% 95.89%

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.
Dysphania ambrosioides

Cross-Links

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PubChem 564367
LOTUS LTS0264944
wikiData Q104969477