4,5-Bis(hydroxymethyl)-3-methoxy-2-methylphenol

Details

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Internal ID 0e7fbaa9-a808-47d4-93e7-775e37f1add3
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4,5-bis(hydroxymethyl)-3-methoxy-2-methylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O4/c1-6-9(13)3-7(4-11)8(5-12)10(6)14-2/h3,11-13H,4-5H2,1-2H3
InChI Key SBITWTIJPCFPQA-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 0.10
Atomic LogP (AlogP) 0.69
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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148717-78-6
4,5-Bis(hydroxymethyl)-3-methoxy-2-methylphenol
5-hydroxy-3-methoxy-4-methyl-1,2-benzenedimethanol
(5-Hydroxy-3-methoxy-4-methyl-1,2-phenylene)dimethanol
BS-1551

2D Structure

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2D Structure of 4,5-Bis(hydroxymethyl)-3-methoxy-2-methylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9393 93.93%
Caco-2 - 0.5534 55.34%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8919 89.19%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.8490 84.90%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9550 95.50%
P-glycoprotein inhibitior - 0.9484 94.84%
P-glycoprotein substrate - 0.9656 96.56%
CYP3A4 substrate - 0.5851 58.51%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate + 0.3474 34.74%
CYP3A4 inhibition - 0.5754 57.54%
CYP2C9 inhibition - 0.8682 86.82%
CYP2C19 inhibition - 0.5283 52.83%
CYP2D6 inhibition - 0.8818 88.18%
CYP1A2 inhibition + 0.5097 50.97%
CYP2C8 inhibition - 0.8117 81.17%
CYP inhibitory promiscuity + 0.5113 51.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6963 69.63%
Carcinogenicity (trinary) Non-required 0.6853 68.53%
Eye corrosion - 0.9395 93.95%
Eye irritation + 0.7985 79.85%
Skin irritation - 0.7383 73.83%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5954 59.54%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5965 59.65%
skin sensitisation + 0.5184 51.84%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5164 51.64%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7986 79.86%
Acute Oral Toxicity (c) III 0.7470 74.70%
Estrogen receptor binding - 0.5960 59.60%
Androgen receptor binding - 0.6433 64.33%
Thyroid receptor binding - 0.7376 73.76%
Glucocorticoid receptor binding - 0.7305 73.05%
Aromatase binding - 0.7202 72.02%
PPAR gamma - 0.6249 62.49%
Honey bee toxicity - 0.9585 95.85%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8337 83.37%

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 97.88% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.47% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.49% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 87.24% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.60% 95.56%
CHEMBL4208 P20618 Proteasome component C5 85.94% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.80% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.65% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.90% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.42% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.02% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.88% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.63% 92.62%

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 85691048
LOTUS LTS0038441
wikiData Q105249478