5,7-Dihydroxy-2-(6-phenylhexyl)-gamma-chromene-4-one

Details

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Internal ID f048643a-e4aa-4382-9f45-878098879590
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5,7-dihydroxy-2-(6-phenylhexyl)chromen-4-one
SMILES (Canonical) C1=CC=C(C=C1)CCCCCCC2=CC(=O)C3=C(C=C(C=C3O2)O)O
SMILES (Isomeric) C1=CC=C(C=C1)CCCCCCC2=CC(=O)C3=C(C=C(C=C3O2)O)O
InChI InChI=1S/C21H22O4/c22-16-12-18(23)21-19(24)14-17(25-20(21)13-16)11-7-2-1-4-8-15-9-5-3-6-10-15/h3,5-6,9-10,12-14,22-23H,1-2,4,7-8,11H2
InChI Key FLHVQRQJWZFNJO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O4
Molecular Weight 338.40 g/mol
Exact Mass 338.15180918 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.55
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 5,7-Dihydroxy-2-(6-phenylhexyl)-gamma-chromene-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 + 0.9317 93.17%
Caco-2 - 0.5487 54.87%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5643 56.43%
OATP2B1 inhibitior - 0.7161 71.61%
OATP1B1 inhibitior + 0.9031 90.31%
OATP1B3 inhibitior + 0.9559 95.59%
MATE1 inhibitior - 0.5200 52.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5124 51.24%
P-glycoprotein inhibitior + 0.6646 66.46%
P-glycoprotein substrate - 0.7764 77.64%
CYP3A4 substrate + 0.5288 52.88%
CYP2C9 substrate - 0.5642 56.42%
CYP2D6 substrate - 0.8131 81.31%
CYP3A4 inhibition + 0.9135 91.35%
CYP2C9 inhibition - 0.6297 62.97%
CYP2C19 inhibition + 0.5863 58.63%
CYP2D6 inhibition - 0.8309 83.09%
CYP1A2 inhibition + 0.7412 74.12%
CYP2C8 inhibition + 0.7008 70.08%
CYP inhibitory promiscuity - 0.5332 53.32%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6713 67.13%
Eye corrosion - 0.9765 97.65%
Eye irritation - 0.5447 54.47%
Skin irritation - 0.6944 69.44%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7326 73.26%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.6069 60.69%
skin sensitisation - 0.8428 84.28%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7126 71.26%
Acute Oral Toxicity (c) III 0.7970 79.70%
Estrogen receptor binding + 0.9144 91.44%
Androgen receptor binding + 0.8828 88.28%
Thyroid receptor binding + 0.5267 52.67%
Glucocorticoid receptor binding + 0.7053 70.53%
Aromatase binding + 0.7462 74.62%
PPAR gamma + 0.8565 85.65%
Honey bee toxicity - 0.8880 88.80%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5350 53.50%
Fish aquatic toxicity + 0.8224 82.24%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.39% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.04% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.80% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 92.67% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.68% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.69% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.51% 99.17%
CHEMBL3194 P02766 Transthyretin 87.49% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.63% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.57% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 83.95% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.32% 89.00%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 80.10% 100.00%

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.
Cnidoscolus texanus
Diospyros montana
Dracaena hanningtonii
Flaveria bidentis
Horsfieldia irya
Hymenaea oblongifolia
Lespedeza cyrtobotrya
Ptelea crenulata
Teucrium fragile
Trichilia dregeana
Uvaria ferruginea
Veronica anagallis-aquatica

Cross-Links

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PubChem 101219429
NPASS NPC175611
LOTUS LTS0212986
wikiData Q104997112