Orixinone

Details

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Internal ID 7b14c0e8-d157-409e-8fce-0f6fbaa88369
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives
IUPAC Name 1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutan-2-one
SMILES (Canonical) CC(C)C(=O)CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC
SMILES (Isomeric) CC(C)C(=O)CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC
InChI InChI=1S/C17H19NO5/c1-9(2)12(19)7-11-15(20-3)10-5-6-13-16(23-8-22-13)14(10)18-17(11)21-4/h5-6,9H,7-8H2,1-4H3
InChI Key JNSVENVWIBKRQR-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO5
Molecular Weight 317.34 g/mol
Exact Mass 317.12632271 g/mol
Topological Polar Surface Area (TPSA) 66.90 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL519190
1-(6,8-Dimethoxy-1,3-dioxolo[4,5-h]quinolin-7-yl)-3-methyl-2-butanone

2D Structure

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2D Structure of Orixinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9698 96.98%
Caco-2 + 0.8537 85.37%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6359 63.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9244 92.44%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8123 81.23%
P-glycoprotein inhibitior - 0.7530 75.30%
P-glycoprotein substrate - 0.8508 85.08%
CYP3A4 substrate + 0.5151 51.51%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.7539 75.39%
CYP3A4 inhibition + 0.8218 82.18%
CYP2C9 inhibition - 0.6571 65.71%
CYP2C19 inhibition - 0.5404 54.04%
CYP2D6 inhibition - 0.8847 88.47%
CYP1A2 inhibition + 0.8130 81.30%
CYP2C8 inhibition - 0.8159 81.59%
CYP inhibitory promiscuity + 0.7979 79.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5874 58.74%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.7922 79.22%
Skin irritation - 0.8303 83.03%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis + 0.6046 60.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6102 61.02%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.8115 81.15%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6634 66.34%
Acute Oral Toxicity (c) III 0.6387 63.87%
Estrogen receptor binding + 0.7838 78.38%
Androgen receptor binding + 0.5568 55.68%
Thyroid receptor binding + 0.7001 70.01%
Glucocorticoid receptor binding + 0.8975 89.75%
Aromatase binding + 0.5487 54.87%
PPAR gamma + 0.7672 76.72%
Honey bee toxicity - 0.9023 90.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6555 65.55%
Fish aquatic toxicity + 0.6858 68.58%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.31% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.03% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.49% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.99% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.78% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.53% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.23% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.33% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.95% 95.56%
CHEMBL2535 P11166 Glucose transporter 85.54% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.62% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.29% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.64% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.27% 94.80%

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.
Orixa japonica

Cross-Links

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PubChem 5320309
NPASS NPC31289
LOTUS LTS0149997
wikiData Q104398944