2-Methylbenzyl alcohol

Details

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Internal ID 2f82a168-ef14-47a6-b4fc-7da0287d9b60
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name (2-methylphenyl)methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O/c1-7-4-2-3-5-8(7)6-9/h2-5,9H,6H2,1H3
InChI Key XPNGNIFUDRPBFJ-UHFFFAOYSA-N
Popularity 266 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O
Molecular Weight 122.16 g/mol
Exact Mass 122.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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89-95-2
o-tolylmethanol
(2-Methylphenyl)methanol
o-Methylbenzyl alcohol
Benzenemethanol, 2-methyl-
7L3M6Y04NC
NSC-91
DTXSID8059001
ortho-methylbenzyl alcohol
RefChem:475979
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Methylbenzyl alcohol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9776 97.76%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5805 58.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9527 95.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8857 88.57%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9767 97.67%
CYP3A4 substrate - 0.7092 70.92%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.7054 70.54%
CYP3A4 inhibition - 0.9326 93.26%
CYP2C9 inhibition - 0.9146 91.46%
CYP2C19 inhibition - 0.7873 78.73%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition + 0.5877 58.77%
CYP2C8 inhibition - 0.9514 95.14%
CYP inhibitory promiscuity - 0.7989 79.89%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.7417 74.17%
Eye corrosion + 0.8607 86.07%
Eye irritation + 0.9888 98.88%
Skin irritation + 0.8491 84.91%
Skin corrosion - 0.6024 60.24%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7496 74.96%
Micronuclear - 0.8651 86.51%
Hepatotoxicity - 0.5372 53.72%
skin sensitisation + 0.8554 85.54%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6564 65.64%
Acute Oral Toxicity (c) III 0.7536 75.36%
Estrogen receptor binding - 0.9405 94.05%
Androgen receptor binding - 0.8860 88.60%
Thyroid receptor binding - 0.9053 90.53%
Glucocorticoid receptor binding - 0.9218 92.18%
Aromatase binding - 0.8535 85.35%
PPAR gamma - 0.8659 86.59%
Honey bee toxicity - 0.9909 99.09%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8560 85.60%

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 92.55% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.67% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.63% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.17% 96.25%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.94% 93.65%

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.
Scutellaria baicalensis

Cross-Links

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PubChem 6994
LOTUS LTS0027631
wikiData Q27268494