Imperanene

Details

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Internal ID 4fb59549-f689-4992-b048-0dc7b6ca63eb
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 4-[(E,2S)-4-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)but-3-enyl]-2-methoxyphenol
SMILES (Canonical) COC1=C(C=CC(=C1)CC(CO)C=CC2=CC(=C(C=C2)O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C[C@H](CO)/C=C/C2=CC(=C(C=C2)O)OC)O
InChI InChI=1S/C19H22O5/c1-23-18-10-13(5-7-16(18)21)3-4-15(12-20)9-14-6-8-17(22)19(11-14)24-2/h3-8,10-11,15,20-22H,9,12H2,1-2H3/b4-3+/t15-/m1/s1
InChI Key RCQPYMXHGRTMOZ-NHZBNJEXSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O5
Molecular Weight 330.40 g/mol
Exact Mass 330.14672380 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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(S)-(+)-Imperanene
CHEMBL476080
HY-N11929
CS-0889974
4-[(E,2S)-4-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)but-3-enyl]-2-methoxyphenol

2D Structure

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2D Structure of Imperanene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 + 0.5709 57.09%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8130 81.30%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8998 89.98%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5876 58.76%
P-glycoprotein inhibitior - 0.4898 48.98%
P-glycoprotein substrate - 0.8624 86.24%
CYP3A4 substrate - 0.5372 53.72%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.6629 66.29%
CYP3A4 inhibition + 0.5263 52.63%
CYP2C9 inhibition - 0.5458 54.58%
CYP2C19 inhibition + 0.7012 70.12%
CYP2D6 inhibition - 0.8497 84.97%
CYP1A2 inhibition + 0.7709 77.09%
CYP2C8 inhibition + 0.7189 71.89%
CYP inhibitory promiscuity + 0.7505 75.05%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7887 78.87%
Carcinogenicity (trinary) Non-required 0.7462 74.62%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.8786 87.86%
Skin irritation - 0.8160 81.60%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6915 69.15%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6821 68.21%
skin sensitisation - 0.5899 58.99%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.8833 88.33%
Acute Oral Toxicity (c) III 0.7434 74.34%
Estrogen receptor binding + 0.8377 83.77%
Androgen receptor binding + 0.7006 70.06%
Thyroid receptor binding + 0.7631 76.31%
Glucocorticoid receptor binding + 0.7146 71.46%
Aromatase binding + 0.6633 66.33%
PPAR gamma + 0.6558 65.58%
Honey bee toxicity - 0.8725 87.25%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9601 96.01%

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 97.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.82% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 93.67% 91.49%
CHEMBL1255126 O15151 Protein Mdm4 93.02% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.89% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.23% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.92% 96.00%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.30% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.72% 90.24%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.65% 91.71%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.49% 89.62%
CHEMBL3194 P02766 Transthyretin 87.55% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.79% 95.50%
CHEMBL2535 P11166 Glucose transporter 84.48% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.23% 95.89%

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.
Imperata cylindrica

Cross-Links

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PubChem 10903632
LOTUS LTS0141620
wikiData Q105233879