5-Nona-3,5-dienylbenzene-1,3-diol

Details

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Internal ID 42c2eb3f-b98b-4a40-ad48-91c689a49144
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 5-nona-3,5-dienylbenzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-2-3-4-5-6-7-8-9-13-10-14(16)12-15(17)11-13/h4-7,10-12,16-17H,2-3,8-9H2,1H3
InChI Key OKTHKZQEUMDKTD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Nona-3,5-dienylbenzene-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 + 0.9822 98.22%
Caco-2 + 0.8693 86.93%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5854 58.54%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8168 81.68%
OATP1B3 inhibitior + 0.9691 96.91%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.4929 49.29%
P-glycoprotein inhibitior - 0.9165 91.65%
P-glycoprotein substrate - 0.8794 87.94%
CYP3A4 substrate - 0.6378 63.78%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate - 0.6697 66.97%
CYP3A4 inhibition + 0.7967 79.67%
CYP2C9 inhibition + 0.5293 52.93%
CYP2C19 inhibition + 0.6461 64.61%
CYP2D6 inhibition - 0.7825 78.25%
CYP1A2 inhibition + 0.7701 77.01%
CYP2C8 inhibition - 0.6627 66.27%
CYP inhibitory promiscuity + 0.8162 81.62%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7011 70.11%
Carcinogenicity (trinary) Non-required 0.6099 60.99%
Eye corrosion + 0.6033 60.33%
Eye irritation + 0.9242 92.42%
Skin irritation + 0.6869 68.69%
Skin corrosion + 0.7567 75.67%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4006 40.06%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.8789 87.89%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6071 60.71%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6456 64.56%
Acute Oral Toxicity (c) III 0.5647 56.47%
Estrogen receptor binding + 0.7747 77.47%
Androgen receptor binding + 0.5337 53.37%
Thyroid receptor binding + 0.5922 59.22%
Glucocorticoid receptor binding + 0.5497 54.97%
Aromatase binding + 0.6793 67.93%
PPAR gamma + 0.8209 82.09%
Honey bee toxicity - 0.9717 97.17%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8645 86.45%

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
CHEMBL2581 P07339 Cathepsin D 92.14% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.92% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.75% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.49% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.14% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.69% 92.08%

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 73062306
LOTUS LTS0210847
wikiData Q104193466