beta,beta-Dimethylbenzeneethanol

Details

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Internal ID 6dab6ed8-6107-43d6-b146-c836c46bc261
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 2-methyl-2-phenylpropan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-10(2,8-11)9-6-4-3-5-7-9/h3-7,11H,8H2,1-2H3
InChI Key ZVSCENGNXWPDPL-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2173-69-5
2-methyl-2-phenyl-1-propanol
2-methyl-2-phenyl-propan-1-ol
MFCD00506139
2-methyl-2-phenylpropanol
Benzeneethanol, b,b-dimethyl-
NSC956
2-methyl-2-phenyl-propanol
SCHEMBL300764
2-phenyl-2-methylpropyl alcohol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta,beta-Dimethylbenzeneethanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9682 96.82%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5677 56.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8450 84.50%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9364 93.64%
CYP3A4 substrate - 0.7952 79.52%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7336 73.36%
CYP3A4 inhibition - 0.7718 77.18%
CYP2C9 inhibition - 0.8880 88.80%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.9035 90.35%
CYP1A2 inhibition - 0.6003 60.03%
CYP2C8 inhibition - 0.9176 91.76%
CYP inhibitory promiscuity - 0.8866 88.66%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5817 58.17%
Carcinogenicity (trinary) Non-required 0.6644 66.44%
Eye corrosion + 0.8214 82.14%
Eye irritation + 0.9515 95.15%
Skin irritation + 0.7240 72.40%
Skin corrosion - 0.8957 89.57%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7954 79.54%
Micronuclear - 0.9541 95.41%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation + 0.7622 76.22%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6044 60.44%
Acute Oral Toxicity (c) III 0.9065 90.65%
Estrogen receptor binding - 0.9322 93.22%
Androgen receptor binding - 0.8617 86.17%
Thyroid receptor binding - 0.7846 78.46%
Glucocorticoid receptor binding - 0.9375 93.75%
Aromatase binding - 0.8646 86.46%
PPAR gamma - 0.8475 84.75%
Honey bee toxicity - 0.9890 98.90%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.7891 78.91%

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
CHEMBL2581 P07339 Cathepsin D 92.98% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.46% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.65% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.37% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.05% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.42% 86.33%

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.
Glycyrrhiza glabra

Cross-Links

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PubChem 219535
LOTUS LTS0178647
wikiData Q82008100