phenylmethan(18O)ol

Details

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Internal ID fdccb679-2e06-46bd-8116-ca57b0f7bed8
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name phenylmethan(18O)ol
SMILES (Canonical) C1=CC=C(C=C1)CO
SMILES (Isomeric) C1=CC=C(C=C1)C[18OH]
InChI InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2/i8+2
InChI Key WVDDGKGOMKODPV-PPJXEINESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O
Molecular Weight 110.14 g/mol
Exact Mass 110.061759867 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 1
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 phenylmethan(18O)ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9601 96.01%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Mitochondria 0.4584 45.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9066 90.66%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9870 98.70%
CYP3A4 substrate - 0.8216 82.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6770 67.70%
CYP3A4 inhibition - 0.9558 95.58%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.7859 78.59%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition + 0.5434 54.34%
CYP2C8 inhibition - 0.8581 85.81%
CYP inhibitory promiscuity - 0.8458 84.58%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.5617 56.17%
Carcinogenicity (trinary) Non-required 0.7056 70.56%
Eye corrosion + 0.9541 95.41%
Eye irritation + 0.9937 99.37%
Skin irritation + 0.9390 93.90%
Skin corrosion + 0.6767 67.67%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8691 86.91%
Micronuclear - 0.7182 71.82%
Hepatotoxicity + 0.6807 68.07%
skin sensitisation + 0.8582 85.82%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5052 50.52%
Acute Oral Toxicity (c) III 0.8069 80.69%
Estrogen receptor binding - 0.8681 86.81%
Androgen receptor binding - 0.8680 86.80%
Thyroid receptor binding - 0.8739 87.39%
Glucocorticoid receptor binding - 0.8696 86.96%
Aromatase binding - 0.7821 78.21%
PPAR gamma - 0.7863 78.63%
Honey bee toxicity - 0.9477 94.77%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity - 0.5253 52.53%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 20 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 90.39% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.69% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.25% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.01% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.66% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.23% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.56% 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.
Chaenomeles sinensis
Cicuta virosa
Citrus × aurantium
Curcuma longa
Lonicera japonica
Prunus mume
Prunus persica
Uncaria macrophylla

Cross-Links

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PubChem 11062333
NPASS NPC278112