3-Heptadec-10-enyl-4,5-dimethoxyphenol

Details

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Internal ID 426a4c85-a2ef-47d4-af58-750c45fd5ac7
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-heptadec-10-enyl-4,5-dimethoxyphenol
SMILES (Canonical) CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)OC
SMILES (Isomeric) CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)OC
InChI InChI=1S/C25H42O3/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20-23(26)21-24(27-2)25(22)28-3/h9-10,20-21,26H,4-8,11-19H2,1-3H3
InChI Key HQCYNCIUHBEAHB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42O3
Molecular Weight 390.60 g/mol
Exact Mass 390.31339520 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 9.50
Atomic LogP (AlogP) 7.60
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Heptadec-10-enyl-4,5-dimethoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.6862 68.62%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7695 76.95%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8224 82.24%
OATP1B3 inhibitior + 0.9396 93.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8961 89.61%
P-glycoprotein inhibitior + 0.6391 63.91%
P-glycoprotein substrate - 0.7521 75.21%
CYP3A4 substrate + 0.5213 52.13%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.6639 66.39%
CYP2C9 inhibition - 0.8049 80.49%
CYP2C19 inhibition + 0.5548 55.48%
CYP2D6 inhibition - 0.8258 82.58%
CYP1A2 inhibition + 0.6061 60.61%
CYP2C8 inhibition + 0.8685 86.85%
CYP inhibitory promiscuity + 0.5200 52.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7786 77.86%
Carcinogenicity (trinary) Non-required 0.6697 66.97%
Eye corrosion - 0.9313 93.13%
Eye irritation - 0.6848 68.48%
Skin irritation - 0.6121 61.21%
Skin corrosion - 0.8389 83.89%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8231 82.31%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6881 68.81%
skin sensitisation + 0.5689 56.89%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.7249 72.49%
Acute Oral Toxicity (c) III 0.6846 68.46%
Estrogen receptor binding + 0.7394 73.94%
Androgen receptor binding + 0.6156 61.56%
Thyroid receptor binding + 0.5415 54.15%
Glucocorticoid receptor binding + 0.5620 56.20%
Aromatase binding - 0.5995 59.95%
PPAR gamma + 0.5974 59.74%
Honey bee toxicity - 0.9586 95.86%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.8896 88.96%
Fish aquatic toxicity + 0.9939 99.39%

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 98.39% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.37% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.84% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.17% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.45% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.34% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 90.94% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.83% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.52% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.31% 89.62%
CHEMBL240 Q12809 HERG 84.31% 89.76%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.90% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.60% 93.99%
CHEMBL2885 P07451 Carbonic anhydrase III 83.51% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.28% 95.56%
CHEMBL3891 P07384 Calpain 1 82.07% 93.04%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.98% 91.81%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.96% 92.62%
CHEMBL2535 P11166 Glucose transporter 81.93% 98.75%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.85% 82.38%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.71% 92.68%
CHEMBL1907 P15144 Aminopeptidase N 80.89% 93.31%

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.
Iris missouriensis

Cross-Links

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PubChem 78144896
LOTUS LTS0050495
wikiData Q105032185