3-(2-Hydroxyethoxy)-9H-xanthen-9-one

Details

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Internal ID 6de4e3d4-75d2-4384-a588-09979badaf67
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3-(2-hydroxyethoxy)xanthen-9-one
SMILES (Canonical) C1=CC=C2C(=C1)C(=O)C3=C(O2)C=C(C=C3)OCCO
SMILES (Isomeric) C1=CC=C2C(=C1)C(=O)C3=C(O2)C=C(C=C3)OCCO
InChI InChI=1S/C15H12O4/c16-7-8-18-10-5-6-12-14(9-10)19-13-4-2-1-3-11(13)15(12)17/h1-6,9,16H,7-8H2
InChI Key SCGUXZHIYPNDEG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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646063-94-7
DTXSID10802032
RefChem:273718
DTXCID60752775
3-(2-hydroxyethoxy) xanthone

2D Structure

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2D Structure of 3-(2-Hydroxyethoxy)-9H-xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9726 97.26%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6582 65.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9244 92.44%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5552 55.52%
P-glycoprotein inhibitior - 0.5924 59.24%
P-glycoprotein substrate - 0.9209 92.09%
CYP3A4 substrate + 0.5426 54.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7715 77.15%
CYP3A4 inhibition - 0.7477 74.77%
CYP2C9 inhibition - 0.8150 81.50%
CYP2C19 inhibition - 0.5163 51.63%
CYP2D6 inhibition - 0.8708 87.08%
CYP1A2 inhibition + 0.5700 57.00%
CYP2C8 inhibition + 0.6093 60.93%
CYP inhibitory promiscuity - 0.6744 67.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5413 54.13%
Eye corrosion - 0.9749 97.49%
Eye irritation + 0.7917 79.17%
Skin irritation - 0.7406 74.06%
Skin corrosion - 0.9758 97.58%
Ames mutagenesis - 0.5870 58.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6493 64.93%
Micronuclear - 0.6141 61.41%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8298 82.98%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4721 47.21%
Acute Oral Toxicity (c) III 0.6699 66.99%
Estrogen receptor binding + 0.9358 93.58%
Androgen receptor binding + 0.9467 94.67%
Thyroid receptor binding + 0.5803 58.03%
Glucocorticoid receptor binding + 0.9026 90.26%
Aromatase binding + 0.9372 93.72%
PPAR gamma + 0.9314 93.14%
Honey bee toxicity - 0.8816 88.16%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.7856 78.56%

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 99.38% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.87% 94.00%
CHEMBL2039 P27338 Monoamine oxidase B 94.14% 92.51%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.50% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.36% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.10% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.57% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.95% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 88.45% 92.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.97% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.64% 99.15%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.22% 94.62%
CHEMBL4531 P17931 Galectin-3 84.57% 96.90%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.11% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 82.10% 93.31%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.93% 86.92%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.51% 95.50%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.26% 80.78%
CHEMBL4302 P08183 P-glycoprotein 1 80.65% 92.98%

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.
Hedychium gardnerianum

Cross-Links

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PubChem 71379467
LOTUS LTS0158417
wikiData Q82775546