1-(2,4,6-Trihydroxyphenyl)octadeca-6,9,12,15-tetraen-1-one

Details

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Internal ID 1bc3d282-97fa-4838-9a58-3844717314c1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,4,6-trihydroxyphenyl)octadeca-6,9,12,15-tetraen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H32O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(26)24-22(27)18-20(25)19-23(24)28/h3-4,6-7,9-10,12-13,18-19,25,27-28H,2,5,8,11,14-17H2,1H3
InChI Key JPYHHZQJCSQRJY-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H32O4
Molecular Weight 384.50 g/mol
Exact Mass 384.23005950 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.35
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,4,6-Trihydroxyphenyl)octadeca-6,9,12,15-tetraen-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 + 0.9697 96.97%
Caco-2 - 0.7223 72.23%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8759 87.59%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior - 0.3462 34.62%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8338 83.38%
BSEP inhibitior + 0.7520 75.20%
P-glycoprotein inhibitior + 0.7682 76.82%
P-glycoprotein substrate - 0.8733 87.33%
CYP3A4 substrate - 0.5873 58.73%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8310 83.10%
CYP3A4 inhibition + 0.7903 79.03%
CYP2C9 inhibition + 0.5160 51.60%
CYP2C19 inhibition + 0.6540 65.40%
CYP2D6 inhibition - 0.7966 79.66%
CYP1A2 inhibition + 0.6441 64.41%
CYP2C8 inhibition - 0.6563 65.63%
CYP inhibitory promiscuity + 0.6318 63.18%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8134 81.34%
Carcinogenicity (trinary) Non-required 0.7416 74.16%
Eye corrosion - 0.9531 95.31%
Eye irritation - 0.8056 80.56%
Skin irritation - 0.5261 52.61%
Skin corrosion - 0.9051 90.51%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7923 79.23%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.6965 69.65%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5701 57.01%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8031 80.31%
Acute Oral Toxicity (c) III 0.7490 74.90%
Estrogen receptor binding + 0.8468 84.68%
Androgen receptor binding - 0.5054 50.54%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6477 64.77%
Aromatase binding + 0.5930 59.30%
PPAR gamma + 0.8270 82.70%
Honey bee toxicity - 0.9776 97.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9809 98.09%

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 97.05% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.95% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.08% 91.11%
CHEMBL4208 P20618 Proteasome component C5 87.00% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.76% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.34% 89.00%

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 74052109
LOTUS LTS0237944
wikiData Q104169770