5-O-Ethylhirsutanonol

Details

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Internal ID 75921132-7220-4a67-9a80-231576b4a466
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (5S)-1,7-bis(3,4-dihydroxyphenyl)-5-ethoxyheptan-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H26O6/c1-2-27-17(8-4-15-6-10-19(24)21(26)12-15)13-16(22)7-3-14-5-9-18(23)20(25)11-14/h5-6,9-12,17,23-26H,2-4,7-8,13H2,1H3/t17-/m0/s1
InChI Key HISINPGPQCFGLB-KRWDZBQOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O6
Molecular Weight 374.40 g/mol
Exact Mass 374.17293854 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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875918-12-0
DTXSID90873740

2D Structure

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2D Structure of 5-O-Ethylhirsutanonol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9574 95.74%
Caco-2 - 0.5787 57.87%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9570 95.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9262 92.62%
P-glycoprotein inhibitior - 0.4370 43.70%
P-glycoprotein substrate - 0.7357 73.57%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition - 0.7936 79.36%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.6873 68.73%
CYP2D6 inhibition - 0.8367 83.67%
CYP1A2 inhibition + 0.8954 89.54%
CYP2C8 inhibition - 0.6406 64.06%
CYP inhibitory promiscuity - 0.5862 58.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6721 67.21%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.7328 73.28%
Skin irritation - 0.7748 77.48%
Skin corrosion - 0.9592 95.92%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8088 80.88%
Micronuclear - 0.7341 73.41%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.6785 67.85%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6335 63.35%
Acute Oral Toxicity (c) III 0.7362 73.62%
Estrogen receptor binding + 0.8941 89.41%
Androgen receptor binding + 0.8113 81.13%
Thyroid receptor binding + 0.6814 68.14%
Glucocorticoid receptor binding + 0.7435 74.35%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6661 66.61%
Honey bee toxicity - 0.8087 80.87%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9891 98.91%

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 97.33% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.05% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.27% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.20% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 89.06% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.11% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.88% 96.95%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 82.59% 100.00%
CHEMBL2535 P11166 Glucose transporter 82.12% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.57% 95.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.94% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.87% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.61% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.30% 95.56%

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 11710535
NPASS NPC156116