5-Hydroxy-2-(8-phenyloctyl)chromen-4-one

Details

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Internal ID 0ae3cf1a-b1e9-4143-8c3a-d801e0e751f8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-2-(8-phenyloctyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H26O3/c24-20-15-10-16-22-23(20)21(25)17-19(26-22)14-9-4-2-1-3-6-11-18-12-7-5-8-13-18/h5,7-8,10,12-13,15-17,24H,1-4,6,9,11,14H2
InChI Key CMLCLJURVZTMAX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O3
Molecular Weight 350.40 g/mol
Exact Mass 350.18819469 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.62
H-Bond Acceptor 3
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 5-Hydroxy-2-(8-phenyloctyl)chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 - 0.6554 65.54%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.5056 50.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9226 92.26%
OATP1B3 inhibitior + 0.9790 97.90%
MATE1 inhibitior - 0.5200 52.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6249 62.49%
P-glycoprotein inhibitior + 0.7989 79.89%
P-glycoprotein substrate - 0.7964 79.64%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5642 56.42%
CYP2D6 substrate - 0.8131 81.31%
CYP3A4 inhibition - 0.5425 54.25%
CYP2C9 inhibition - 0.7238 72.38%
CYP2C19 inhibition + 0.7002 70.02%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition + 0.7820 78.20%
CYP2C8 inhibition + 0.4526 45.26%
CYP inhibitory promiscuity - 0.7712 77.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5620 56.20%
Eye corrosion - 0.9474 94.74%
Eye irritation + 0.5460 54.60%
Skin irritation - 0.6167 61.67%
Skin corrosion - 0.9643 96.43%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7477 74.77%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5069 50.69%
skin sensitisation - 0.7951 79.51%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6669 66.69%
Acute Oral Toxicity (c) III 0.8211 82.11%
Estrogen receptor binding + 0.8309 83.09%
Androgen receptor binding + 0.8004 80.04%
Thyroid receptor binding + 0.6460 64.60%
Glucocorticoid receptor binding + 0.6298 62.98%
Aromatase binding + 0.7090 70.90%
PPAR gamma + 0.7742 77.42%
Honey bee toxicity - 0.9186 91.86%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5250 52.50%
Fish aquatic toxicity + 0.8084 80.84%

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 98.56% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.74% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.35% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 93.72% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.27% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.42% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.96% 94.45%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.18% 94.62%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.61% 92.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.73% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.47% 99.17%
CHEMBL3891 P07384 Calpain 1 80.67% 93.04%

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.
Myristica castaneifolia

Cross-Links

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PubChem 129688855
LOTUS LTS0222363
wikiData Q104964809