8-Hydroperoxy-p-cymene

Details

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Internal ID 755d7710-4694-4e37-b74a-fc7523f35c2a
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1-(2-hydroperoxypropan-2-yl)-4-methylbenzene
SMILES (Canonical) CC1=CC=C(C=C1)C(C)(C)OO
SMILES (Isomeric) CC1=CC=C(C=C1)C(C)(C)OO
InChI InChI=1S/C10H14O2/c1-8-4-6-9(7-5-8)10(2,3)12-11/h4-7,11H,1-3H3
InChI Key YCCHNFGPIFYNTF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3077-71-2
1-(2-hydroperoxypropan-2-yl)-4-methylbenzene
SCHEMBL5545791
DTXSID80435957
YCCHNFGPIFYNTF-UHFFFAOYSA-N

2D Structure

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2D Structure of 8-Hydroperoxy-p-cymene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9786 97.86%
Caco-2 + 0.9657 96.57%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7518 75.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9432 94.32%
OATP1B3 inhibitior + 0.9595 95.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7392 73.92%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9874 98.74%
CYP3A4 substrate - 0.6563 65.63%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate - 0.6915 69.15%
CYP3A4 inhibition - 0.7631 76.31%
CYP2C9 inhibition - 0.7922 79.22%
CYP2C19 inhibition - 0.7875 78.75%
CYP2D6 inhibition - 0.8985 89.85%
CYP1A2 inhibition - 0.8154 81.54%
CYP2C8 inhibition - 0.8950 89.50%
CYP inhibitory promiscuity - 0.8089 80.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5357 53.57%
Carcinogenicity (trinary) Non-required 0.5271 52.71%
Eye corrosion + 0.9610 96.10%
Eye irritation + 0.9778 97.78%
Skin irritation + 0.5700 57.00%
Skin corrosion + 0.7418 74.18%
Ames mutagenesis + 0.6146 61.46%
Human Ether-a-go-go-Related Gene inhibition - 0.7328 73.28%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.5391 53.91%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7276 72.76%
Acute Oral Toxicity (c) III 0.6678 66.78%
Estrogen receptor binding - 0.6861 68.61%
Androgen receptor binding - 0.7791 77.91%
Thyroid receptor binding - 0.7740 77.40%
Glucocorticoid receptor binding - 0.8911 89.11%
Aromatase binding - 0.7128 71.28%
PPAR gamma - 0.7397 73.97%
Honey bee toxicity - 0.9713 97.13%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 0.7096 70.96%

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
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.72% 93.65%
CHEMBL240 Q12809 HERG 91.56% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 88.81% 91.49%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.71% 90.93%
CHEMBL3401 O75469 Pregnane X receptor 83.36% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.84% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.80% 86.33%
CHEMBL2581 P07339 Cathepsin D 82.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.83% 96.09%
CHEMBL2039 P27338 Monoamine oxidase B 81.29% 92.51%

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.
Solenostoma obovatum

Cross-Links

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PubChem 10130134
LOTUS LTS0192351
wikiData Q82251100