5-(Tricos-1-EN-1-YL)benzene-1,3-diol

Details

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Internal ID 8ead6457-276a-4414-b5ab-273bbe57f112
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 5-tricos-1-enylbenzene-1,3-diol
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCC=CC1=CC(=CC(=C1)O)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCC=CC1=CC(=CC(=C1)O)O
InChI InChI=1S/C29H50O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-24-28(30)26-29(31)25-27/h22-26,30-31H,2-21H2,1H3
InChI Key MCDSNVQSEUOTPK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H50O2
Molecular Weight 430.70 g/mol
Exact Mass 430.381080833 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 12.90
Atomic LogP (AlogP) 9.93
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 21

Synonyms

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5-(TRICOS-1-EN-1-YL)BENZENE-1,3-DIOL
DTXSID00847598

2D Structure

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2D Structure of 5-(Tricos-1-EN-1-YL)benzene-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 + 0.9947 99.47%
Caco-2 - 0.6072 60.72%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4432 44.32%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.7960 79.60%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8588 85.88%
BSEP inhibitior - 0.5413 54.13%
P-glycoprotein inhibitior - 0.5990 59.90%
P-glycoprotein substrate - 0.9322 93.22%
CYP3A4 substrate - 0.6221 62.21%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate - 0.6697 66.97%
CYP3A4 inhibition + 0.8019 80.19%
CYP2C9 inhibition - 0.6470 64.70%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7974 79.74%
CYP1A2 inhibition + 0.7439 74.39%
CYP2C8 inhibition - 0.5775 57.75%
CYP inhibitory promiscuity + 0.7561 75.61%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7311 73.11%
Carcinogenicity (trinary) Non-required 0.6446 64.46%
Eye corrosion + 0.5455 54.55%
Eye irritation + 0.6266 62.66%
Skin irritation + 0.7150 71.50%
Skin corrosion + 0.5813 58.13%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6830 68.30%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6157 61.57%
skin sensitisation + 0.8683 86.83%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5372 53.72%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5708 57.08%
Acute Oral Toxicity (c) III 0.8480 84.80%
Estrogen receptor binding + 0.7579 75.79%
Androgen receptor binding + 0.5343 53.43%
Thyroid receptor binding + 0.5609 56.09%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5458 54.58%
PPAR gamma + 0.6815 68.15%
Honey bee toxicity - 0.9793 97.93%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8550 85.50%
Fish aquatic toxicity + 0.9878 98.78%

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 96.86% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.04% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.21% 92.08%
CHEMBL2581 P07339 Cathepsin D 95.01% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.09% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.12% 96.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.94% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.80% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.31% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.47% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 87.24% 91.49%
CHEMBL240 Q12809 HERG 86.92% 89.76%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.85% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.13% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.83% 92.68%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.81% 97.21%
CHEMBL242 Q92731 Estrogen receptor beta 80.59% 98.35%

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.
Triticum aestivum

Cross-Links

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PubChem 71428886
LOTUS LTS0118876
wikiData Q82839777