5-Undeca-2,5-dienylbenzene-1,3-diol

Details

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Internal ID 26013b7b-6a00-43f0-9af0-38aa003d8819
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 5-undeca-2,5-dienylbenzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24O2/c1-2-3-4-5-6-7-8-9-10-11-15-12-16(18)14-17(19)13-15/h6-7,9-10,12-14,18-19H,2-5,8,11H2,1H3
InChI Key CPVMKSWWHSPLON-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O2
Molecular Weight 260.40 g/mol
Exact Mass 260.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.72
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Undeca-2,5-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 + 0.9906 99.06%
Caco-2 + 0.9147 91.47%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5227 52.27%
OATP2B1 inhibitior - 0.7158 71.58%
OATP1B1 inhibitior - 0.4489 44.89%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.6245 62.45%
P-glycoprotein inhibitior - 0.8101 81.01%
P-glycoprotein substrate - 0.8233 82.33%
CYP3A4 substrate - 0.6124 61.24%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3567 35.67%
CYP3A4 inhibition + 0.8505 85.05%
CYP2C9 inhibition - 0.5926 59.26%
CYP2C19 inhibition + 0.5358 53.58%
CYP2D6 inhibition - 0.7401 74.01%
CYP1A2 inhibition + 0.7543 75.43%
CYP2C8 inhibition + 0.5680 56.80%
CYP inhibitory promiscuity + 0.8169 81.69%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7411 74.11%
Carcinogenicity (trinary) Non-required 0.6401 64.01%
Eye corrosion + 0.4493 44.93%
Eye irritation + 0.8710 87.10%
Skin irritation + 0.7645 76.45%
Skin corrosion + 0.6007 60.07%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7042 70.42%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8229 82.29%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5491 54.91%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6785 67.85%
Acute Oral Toxicity (c) III 0.7916 79.16%
Estrogen receptor binding + 0.8874 88.74%
Androgen receptor binding - 0.6253 62.53%
Thyroid receptor binding + 0.7510 75.10%
Glucocorticoid receptor binding + 0.6582 65.82%
Aromatase binding + 0.6257 62.57%
PPAR gamma + 0.9589 95.89%
Honey bee toxicity - 0.9912 99.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7246 72.46%
Fish aquatic toxicity + 0.9895 98.95%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.88% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.86% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.75% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.24% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.25% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.80% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.64% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.19% 96.95%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 83.40% 90.75%
CHEMBL240 Q12809 HERG 81.52% 89.76%
CHEMBL1781 P11387 DNA topoisomerase I 81.04% 97.00%

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 85995281
LOTUS LTS0136957
wikiData Q104967802