5-(2-hydroxyethyl)-2-methoxycyclohexa-1,3,4-triene-1,3-diol

Details

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Internal ID 3294784d-4a87-4767-8ad6-45fb1e1ccfd2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 5-(2-hydroxyethyl)-2-methoxycyclohexa-1,3,4-triene-1,3-diol
SMILES (Canonical) COC1=C(CC(=C=C1O)CCO)O
SMILES (Isomeric) COC1=C(CC(=C=C1O)CCO)O
InChI InChI=1S/C9H12O4/c1-13-9-7(11)4-6(2-3-10)5-8(9)12/h10-12H,2-4H2,1H3
InChI Key DSAPZXYPJNSRQY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP -1.00
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(2-hydroxyethyl)-2-methoxycyclohexa-1,3,4-triene-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7768 77.68%
Caco-2 + 0.7364 73.64%
Blood Brain Barrier - 0.6629 66.29%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7507 75.07%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.8104 81.04%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6630 66.30%
BSEP inhibitior - 0.9383 93.83%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.8209 82.09%
CYP3A4 substrate - 0.5801 58.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8237 82.37%
CYP3A4 inhibition - 0.8475 84.75%
CYP2C9 inhibition - 0.8556 85.56%
CYP2C19 inhibition - 0.8271 82.71%
CYP2D6 inhibition - 0.8837 88.37%
CYP1A2 inhibition - 0.8150 81.50%
CYP2C8 inhibition - 0.8947 89.47%
CYP inhibitory promiscuity - 0.7710 77.10%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.7527 75.27%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.8736 87.36%
Skin irritation - 0.6912 69.12%
Skin corrosion - 0.9604 96.04%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5979 59.79%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.6736 67.36%
skin sensitisation - 0.6869 68.69%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6779 67.79%
Acute Oral Toxicity (c) III 0.6252 62.52%
Estrogen receptor binding - 0.7146 71.46%
Androgen receptor binding - 0.8838 88.38%
Thyroid receptor binding - 0.5371 53.71%
Glucocorticoid receptor binding - 0.4782 47.82%
Aromatase binding - 0.7989 79.89%
PPAR gamma - 0.7377 73.77%
Honey bee toxicity - 0.9334 93.34%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.7647 76.47%

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 95.67% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.94% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.32% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.57% 93.99%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.39% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.89% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.32% 95.56%

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.
Alphitonia zizyphoides

Cross-Links

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PubChem 133683206
LOTUS LTS0003378
wikiData Q104987744