5-(3-Hydroxypropyl)-3-methoxybenzene-1,2-diol

Details

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Internal ID 5ca8a31d-385b-437d-a64a-2dfd9f5151b2
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 5-(3-hydroxypropyl)-3-methoxybenzene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O4/c1-14-9-6-7(3-2-4-11)5-8(12)10(9)13/h5-6,11-13H,2-4H2,1H3
InChI Key KMSAGIQULZSSAN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O4
Molecular Weight 198.22 g/mol
Exact Mass 198.08920892 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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132473-95-1
AKOS006313489
SB84872
EN300-1870389

2D Structure

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2D Structure of 5-(3-Hydroxypropyl)-3-methoxybenzene-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 + 0.9155 91.55%
Caco-2 + 0.5475 54.75%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8543 85.43%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.7860 78.60%
OATP1B3 inhibitior + 0.9658 96.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9300 93.00%
P-glycoprotein inhibitior - 0.9675 96.75%
P-glycoprotein substrate - 0.7317 73.17%
CYP3A4 substrate - 0.5503 55.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3880 38.80%
CYP3A4 inhibition - 0.9192 91.92%
CYP2C9 inhibition - 0.8601 86.01%
CYP2C19 inhibition - 0.8681 86.81%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition + 0.6300 63.00%
CYP2C8 inhibition + 0.6994 69.94%
CYP inhibitory promiscuity - 0.9299 92.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6930 69.30%
Eye corrosion - 0.9791 97.91%
Eye irritation + 0.9439 94.39%
Skin irritation - 0.6106 61.06%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7082 70.82%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.6947 69.47%
skin sensitisation + 0.5175 51.75%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7327 73.27%
Acute Oral Toxicity (c) III 0.8062 80.62%
Estrogen receptor binding + 0.5322 53.22%
Androgen receptor binding - 0.5193 51.93%
Thyroid receptor binding - 0.6312 63.12%
Glucocorticoid receptor binding - 0.5364 53.64%
Aromatase binding - 0.8464 84.64%
PPAR gamma - 0.6586 65.86%
Honey bee toxicity - 0.9584 95.84%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7049 70.49%
Fish aquatic toxicity - 0.7528 75.28%

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 97.95% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.64% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.65% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.35% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.24% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 85.59% 90.20%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.43% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.81% 94.00%
CHEMBL3194 P02766 Transthyretin 83.40% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.91% 94.45%
CHEMBL2424 Q04760 Glyoxalase I 82.16% 91.67%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.68% 95.89%
CHEMBL2885 P07451 Carbonic anhydrase III 80.66% 87.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.21% 92.62%

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.
Relhania fruticosa

Cross-Links

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PubChem 14733612
LOTUS LTS0213388
wikiData Q105143171