2,4-Dimethoxy-6-pentadec-10-enylphenol

Details

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Internal ID cc243e7c-0f07-467a-9e4b-b4bebcd6d4f5
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2,4-dimethoxy-6-pentadec-10-enylphenol
SMILES (Canonical) CCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)OC)OC)O
SMILES (Isomeric) CCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)OC)OC)O
InChI InChI=1S/C23H38O3/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-18-21(25-2)19-22(26-3)23(20)24/h7-8,18-19,24H,4-6,9-17H2,1-3H3
InChI Key GBCXPDPXQWPCTG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H38O3
Molecular Weight 362.50 g/mol
Exact Mass 362.28209507 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 8.40
Atomic LogP (AlogP) 6.82
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4-Dimethoxy-6-pentadec-10-enylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.6381 63.81%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8068 80.68%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.7607 76.07%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8092 80.92%
P-glycoprotein inhibitior + 0.6413 64.13%
P-glycoprotein substrate - 0.7073 70.73%
CYP3A4 substrate - 0.5207 52.07%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.5965 59.65%
CYP2C9 inhibition - 0.7398 73.98%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8274 82.74%
CYP1A2 inhibition + 0.6756 67.56%
CYP2C8 inhibition + 0.7535 75.35%
CYP inhibitory promiscuity - 0.5137 51.37%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7886 78.86%
Carcinogenicity (trinary) Non-required 0.6554 65.54%
Eye corrosion - 0.9102 91.02%
Eye irritation - 0.6175 61.75%
Skin irritation - 0.6721 67.21%
Skin corrosion - 0.8100 81.00%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7887 78.87%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6540 65.40%
skin sensitisation + 0.5090 50.90%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.7315 73.15%
Acute Oral Toxicity (c) III 0.6682 66.82%
Estrogen receptor binding + 0.8341 83.41%
Androgen receptor binding + 0.6394 63.94%
Thyroid receptor binding + 0.5530 55.30%
Glucocorticoid receptor binding + 0.6089 60.89%
Aromatase binding - 0.5700 57.00%
PPAR gamma + 0.7073 70.73%
Honey bee toxicity - 0.9716 97.16%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6937 69.37%
Fish aquatic toxicity + 0.9942 99.42%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.54% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.93% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.11% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.09% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.20% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.60% 92.62%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 88.34% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.57% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.50% 93.99%
CHEMBL240 Q12809 HERG 86.29% 89.76%
CHEMBL1907 P15144 Aminopeptidase N 85.68% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.66% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.79% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 82.79% 89.63%
CHEMBL4208 P20618 Proteasome component C5 82.41% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.44% 89.62%
CHEMBL2885 P07451 Carbonic anhydrase III 81.34% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.06% 96.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.05% 92.94%

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 domestica

Cross-Links

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PubChem 78385594
LOTUS LTS0103456
wikiData Q105005785