1-(4-Hydroxyphenyl)propane-1,2-diol

Details

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Internal ID 6d1fffd8-e988-417a-ba3e-9c8b29e488b1
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1-(4-hydroxyphenyl)propane-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O3/c1-6(10)9(12)7-2-4-8(11)5-3-7/h2-6,9-12H,1H3
InChI Key PIYCCGIPUXJHIW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O3
Molecular Weight 168.19 g/mol
Exact Mass 168.078644241 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.81
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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p-hydroxyphenylpropylene glycol
SCHEMBL15240610
CHEBI:192580
AKOS040738177
1-(4-HYDROXYPHENYL)PROPANE-1,2-DIOL

2D Structure

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2D Structure of 1-(4-Hydroxyphenyl)propane-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 + 0.6629 66.29%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8450 84.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8418 84.18%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9783 97.83%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.8931 89.31%
CYP3A4 substrate - 0.7674 76.74%
CYP2C9 substrate - 0.7739 77.39%
CYP2D6 substrate - 0.6661 66.61%
CYP3A4 inhibition - 0.9279 92.79%
CYP2C9 inhibition - 0.8874 88.74%
CYP2C19 inhibition - 0.9628 96.28%
CYP2D6 inhibition - 0.9770 97.70%
CYP1A2 inhibition - 0.8997 89.97%
CYP2C8 inhibition - 0.9701 97.01%
CYP inhibitory promiscuity - 0.8875 88.75%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6666 66.66%
Carcinogenicity (trinary) Warning 0.5230 52.30%
Eye corrosion + 0.8295 82.95%
Eye irritation + 0.5367 53.67%
Skin irritation + 0.8743 87.43%
Skin corrosion + 0.8998 89.98%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8098 80.98%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation + 0.8473 84.73%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.5645 56.45%
Acute Oral Toxicity (c) III 0.8243 82.43%
Estrogen receptor binding - 0.9360 93.60%
Androgen receptor binding - 0.6177 61.77%
Thyroid receptor binding - 0.7160 71.60%
Glucocorticoid receptor binding - 0.8852 88.52%
Aromatase binding - 0.8966 89.66%
PPAR gamma - 0.7303 73.03%
Honey bee toxicity - 0.9430 94.30%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.6812 68.12%

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 93.94% 98.35%
CHEMBL301 P24941 Cyclin-dependent kinase 2 93.72% 91.23%
CHEMBL2581 P07339 Cathepsin D 92.69% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.84% 96.09%
CHEMBL4208 P20618 Proteasome component C5 87.27% 90.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.56% 93.10%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.51% 97.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.98% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.15% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.10% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 94.73%

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.
Narvalina domingensis

Cross-Links

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PubChem 75411975
LOTUS LTS0244388
wikiData Q105209794