Ilanenoid

Details

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Internal ID ac9022b8-94a6-45e0-af39-b761befbf410
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Cinnamylphenols
IUPAC Name 2-methoxy-4-[(2R)-2-methoxy-3-(2,4,6-trimethoxyphenyl)propyl]phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O6/c1-22-14(8-13-6-7-17(21)20(9-13)26-5)10-16-18(24-3)11-15(23-2)12-19(16)25-4/h6-7,9,11-12,14,21H,8,10H2,1-5H3/t14-/m1/s1
InChI Key VXOTURNUCJNHEU-CQSZACIVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H26O6
Molecular Weight 362.40 g/mol
Exact Mass 362.17293854 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ilanenoid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9898 98.98%
Caco-2 + 0.9510 95.10%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8115 81.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8670 86.70%
OATP1B3 inhibitior + 0.9045 90.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5967 59.67%
P-glycoprotein inhibitior + 0.7441 74.41%
P-glycoprotein substrate - 0.8533 85.33%
CYP3A4 substrate - 0.5538 55.38%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate + 0.4755 47.55%
CYP3A4 inhibition - 0.8174 81.74%
CYP2C9 inhibition - 0.9323 93.23%
CYP2C19 inhibition + 0.7036 70.36%
CYP2D6 inhibition - 0.7628 76.28%
CYP1A2 inhibition - 0.5210 52.10%
CYP2C8 inhibition + 0.7105 71.05%
CYP inhibitory promiscuity + 0.5190 51.90%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7850 78.50%
Carcinogenicity (trinary) Non-required 0.6653 66.53%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.8271 82.71%
Skin irritation - 0.7989 79.89%
Skin corrosion - 0.9733 97.33%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7593 75.93%
Micronuclear - 0.6182 61.82%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8140 81.40%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7916 79.16%
Acute Oral Toxicity (c) III 0.7340 73.40%
Estrogen receptor binding + 0.8566 85.66%
Androgen receptor binding + 0.5317 53.17%
Thyroid receptor binding + 0.7674 76.74%
Glucocorticoid receptor binding + 0.7953 79.53%
Aromatase binding + 0.5243 52.43%
PPAR gamma + 0.5958 59.58%
Honey bee toxicity - 0.8813 88.13%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6051 60.51%
Fish aquatic toxicity + 0.9435 94.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.19% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.52% 99.15%
CHEMBL2581 P07339 Cathepsin D 92.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.15% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 90.60% 90.24%
CHEMBL4208 P20618 Proteasome component C5 90.24% 90.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.96% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.59% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.04% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.00% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 84.71% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.46% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.03% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.84% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.39% 95.89%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.38% 92.68%
CHEMBL2535 P11166 Glucose transporter 82.37% 98.75%

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 139587458
LOTUS LTS0227298
wikiData Q77566506