(Z)-1-(2,6-dihydroxy-4-methoxyphenyl)oct-5-en-1-one

Details

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Internal ID 03d9a240-c85e-4d5d-ad94-87456203ea88
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name (Z)-1-(2,6-dihydroxy-4-methoxyphenyl)oct-5-en-1-one
SMILES (Canonical) CCC=CCCCC(=O)C1=C(C=C(C=C1O)OC)O
SMILES (Isomeric) CC/C=C\CCCC(=O)C1=C(C=C(C=C1O)OC)O
InChI InChI=1S/C15H20O4/c1-3-4-5-6-7-8-12(16)15-13(17)9-11(19-2)10-14(15)18/h4-5,9-10,17-18H,3,6-8H2,1-2H3/b5-4-
InChI Key ZZIKFTFHMPJATM-PLNGDYQASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O4
Molecular Weight 264.32 g/mol
Exact Mass 264.13615911 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-1-(2,6-dihydroxy-4-methoxyphenyl)oct-5-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9671 96.71%
Caco-2 + 0.8639 86.39%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.9034 90.34%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.7441 74.41%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7838 78.38%
BSEP inhibitior - 0.5068 50.68%
P-glycoprotein inhibitior - 0.8867 88.67%
P-glycoprotein substrate - 0.8930 89.30%
CYP3A4 substrate - 0.5770 57.70%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8099 80.99%
CYP3A4 inhibition + 0.7015 70.15%
CYP2C9 inhibition - 0.6033 60.33%
CYP2C19 inhibition + 0.7428 74.28%
CYP2D6 inhibition - 0.7153 71.53%
CYP1A2 inhibition + 0.6716 67.16%
CYP2C8 inhibition - 0.6523 65.23%
CYP inhibitory promiscuity + 0.6711 67.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7778 77.78%
Carcinogenicity (trinary) Non-required 0.7772 77.72%
Eye corrosion - 0.9621 96.21%
Eye irritation - 0.5809 58.09%
Skin irritation - 0.7405 74.05%
Skin corrosion - 0.9474 94.74%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3871 38.71%
Micronuclear - 0.8141 81.41%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation + 0.4895 48.95%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7923 79.23%
Acute Oral Toxicity (c) III 0.5947 59.47%
Estrogen receptor binding + 0.7463 74.63%
Androgen receptor binding - 0.5502 55.02%
Thyroid receptor binding - 0.5095 50.95%
Glucocorticoid receptor binding + 0.6695 66.95%
Aromatase binding + 0.7892 78.92%
PPAR gamma + 0.8881 88.81%
Honey bee toxicity - 0.9580 95.80%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5345 53.45%
Fish aquatic toxicity + 0.9724 97.24%

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 97.11% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.20% 96.09%
CHEMBL4208 P20618 Proteasome component C5 88.66% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.41% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.49% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.18% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.21% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.91% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.18% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.42% 96.95%

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.
Ephedra equisetina
Morus alba
Syzygium levinei

Cross-Links

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PubChem 11957912
NPASS NPC193691
LOTUS LTS0224593
wikiData Q105386831