4-(1-Hydroxypropyl)phenol;methane

Details

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Internal ID 9631536e-9d64-46be-86c9-1984a3fcc419
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 4-(1-hydroxypropyl)phenol;methane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O2.CH4/c1-2-9(11)7-3-5-8(10)6-4-7;/h3-6,9-11H,2H2,1H3;1H4
InChI Key JYKBFJULHTUCCM-UHFFFAOYSA-N
Popularity 0 references 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) 40.50 Ų
XlogP 0.00
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(1-Hydroxypropyl)phenol;methane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8423 84.23%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7916 79.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3184 31.84%
OATP1B3 inhibitior + 0.9261 92.61%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9719 97.19%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.8908 89.08%
CYP3A4 substrate - 0.7554 75.54%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.4313 43.13%
CYP3A4 inhibition - 0.7849 78.49%
CYP2C9 inhibition - 0.8047 80.47%
CYP2C19 inhibition - 0.5917 59.17%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.5411 54.11%
CYP2C8 inhibition - 0.7349 73.49%
CYP inhibitory promiscuity - 0.7581 75.81%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5384 53.84%
Carcinogenicity (trinary) Non-required 0.6628 66.28%
Eye corrosion + 0.4528 45.28%
Eye irritation + 0.8899 88.99%
Skin irritation + 0.5681 56.81%
Skin corrosion - 0.5819 58.19%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7231 72.31%
Micronuclear - 0.7714 77.14%
Hepatotoxicity - 0.5753 57.53%
skin sensitisation + 0.9127 91.27%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity - 0.5164 51.64%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.7209 72.09%
Acute Oral Toxicity (c) III 0.7964 79.64%
Estrogen receptor binding - 0.8480 84.80%
Androgen receptor binding - 0.7185 71.85%
Thyroid receptor binding - 0.7364 73.64%
Glucocorticoid receptor binding - 0.8872 88.72%
Aromatase binding - 0.8658 86.58%
PPAR gamma - 0.7515 75.15%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.5275 52.75%

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
CHEMBL242 Q92731 Estrogen receptor beta 97.36% 98.35%
CHEMBL2581 P07339 Cathepsin D 95.46% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.06% 91.11%
CHEMBL301 P24941 Cyclin-dependent kinase 2 89.84% 91.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.70% 94.45%
CHEMBL4208 P20618 Proteasome component C5 86.51% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 82.90% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.12% 85.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 53399145
NPASS NPC282434