5-Undec-3-enylbenzene-1,3-diol

Details

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Internal ID db4fb037-0c11-400c-8542-a2c77ba6a6d4
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 5-undec-3-enylbenzene-1,3-diol
SMILES (Canonical) CCCCCCCC=CCCC1=CC(=CC(=C1)O)O
SMILES (Isomeric) CCCCCCCC=CCCC1=CC(=CC(=C1)O)O
InChI InChI=1S/C17H26O2/c1-2-3-4-5-6-7-8-9-10-11-15-12-16(18)14-17(19)13-15/h8-9,12-14,18-19H,2-7,10-11H2,1H3
InChI Key KBZMDBAMUVCKBO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O2
Molecular Weight 262.40 g/mol
Exact Mass 262.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Undec-3-enylbenzene-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 + 0.8622 86.22%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5227 52.27%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.7426 74.26%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.5462 54.62%
P-glycoprotein inhibitior - 0.8617 86.17%
P-glycoprotein substrate - 0.8285 82.85%
CYP3A4 substrate - 0.5894 58.94%
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 + 0.5481 54.81%
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 + 0.8029 80.29%
Skin irritation + 0.7645 76.45%
Skin corrosion + 0.6007 60.07%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8690 86.90%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6089 60.89%
skin sensitisation + 0.8229 82.29%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5491 54.91%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7517 75.17%
Acute Oral Toxicity (c) III 0.7916 79.16%
Estrogen receptor binding + 0.7093 70.93%
Androgen receptor binding + 0.5952 59.52%
Thyroid receptor binding + 0.7337 73.37%
Glucocorticoid receptor binding + 0.5571 55.71%
Aromatase binding + 0.5252 52.52%
PPAR gamma + 0.9275 92.75%
Honey bee toxicity - 0.9899 98.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.8696 86.96%
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 97.28% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.07% 92.08%
CHEMBL2581 P07339 Cathepsin D 97.00% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL240 Q12809 HERG 93.27% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.76% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.58% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.37% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 83.26% 89.63%
CHEMBL1781 P11387 DNA topoisomerase I 83.08% 97.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.57% 100.00%
CHEMBL242 Q92731 Estrogen receptor beta 81.50% 98.35%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.44% 97.29%

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.
Persoonia elliptica

Cross-Links

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PubChem 71437101
LOTUS LTS0251940
wikiData Q105138633