2-Hept-1-enyl-3-(hydroxymethyl)benzene-1,4-diol

Details

Top
Internal ID 92c19a2a-eb4e-4856-9f8b-490d9fd59144
Taxonomy Benzenoids > Phenols > Benzenediols > Hydroquinones
IUPAC Name 2-hept-1-enyl-3-(hydroxymethyl)benzene-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O3/c1-2-3-4-5-6-7-11-12(10-15)14(17)9-8-13(11)16/h6-9,15-17H,2-5,10H2,1H3
InChI Key PTXOZTNDVQYKHC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H20O3
Molecular Weight 236.31 g/mol
Exact Mass 236.14124450 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Hept-1-enyl-3-(hydroxymethyl)benzene-1,4-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.7855 78.55%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8210 82.10%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.7182 71.82%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7588 75.88%
BSEP inhibitior - 0.8576 85.76%
P-glycoprotein inhibitior - 0.9346 93.46%
P-glycoprotein substrate - 0.8851 88.51%
CYP3A4 substrate - 0.6372 63.72%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7105 71.05%
CYP3A4 inhibition + 0.6777 67.77%
CYP2C9 inhibition - 0.5858 58.58%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7447 74.47%
CYP1A2 inhibition + 0.8083 80.83%
CYP2C8 inhibition - 0.7389 73.89%
CYP inhibitory promiscuity + 0.7607 76.07%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8423 84.23%
Carcinogenicity (trinary) Non-required 0.7058 70.58%
Eye corrosion - 0.9442 94.42%
Eye irritation + 0.8015 80.15%
Skin irritation + 0.5212 52.12%
Skin corrosion - 0.8161 81.61%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6767 67.67%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7199 71.99%
skin sensitisation + 0.6993 69.93%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7999 79.99%
Acute Oral Toxicity (c) III 0.7273 72.73%
Estrogen receptor binding + 0.6568 65.68%
Androgen receptor binding + 0.5671 56.71%
Thyroid receptor binding + 0.5153 51.53%
Glucocorticoid receptor binding + 0.5787 57.87%
Aromatase binding - 0.6706 67.06%
PPAR gamma + 0.8679 86.79%
Honey bee toxicity - 0.9881 98.81%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6395 63.95%
Fish aquatic toxicity + 0.9884 98.84%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 95.18% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.33% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.38% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.03% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.33% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.29% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 87.62% 91.49%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 86.69% 91.79%
CHEMBL3401 O75469 Pregnane X receptor 85.95% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.79% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.76% 96.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.02% 91.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.27% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.64% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.51% 96.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 163010414
LOTUS LTS0081160
wikiData Q104195424