1,3-Dioxolo(4,5-g)furo(2,3-b)quinoline, 9-methoxy-4-((3-methyl-2-butenyl)oxy)-

Details

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Internal ID cd319867-e61d-479b-be7c-85ebf152bee3
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Furanoquinolines
IUPAC Name 8-methoxy-16-(3-methylbut-2-enoxy)-4,12,14-trioxa-2-azatetracyclo[7.7.0.03,7.011,15]hexadeca-1(16),2,5,7,9,11(15)-hexaene
SMILES (Canonical) CC(=CCOC1=C2C(=CC3=C1OCO3)C(=C4C=COC4=N2)OC)C
SMILES (Isomeric) CC(=CCOC1=C2C(=CC3=C1OCO3)C(=C4C=COC4=N2)OC)C
InChI InChI=1S/C18H17NO5/c1-10(2)4-6-21-17-14-12(8-13-16(17)24-9-23-13)15(20-3)11-5-7-22-18(11)19-14/h4-5,7-8H,6,9H2,1-3H3
InChI Key YFRPSLMDAOYKNS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H17NO5
Molecular Weight 327.30 g/mol
Exact Mass 327.11067264 g/mol
Topological Polar Surface Area (TPSA) 63.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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1,3-Dioxolo(4,5-g)furo(2,3-b)quinoline, 9-methoxy-4-((3-methyl-2-butenyl)oxy)-
NSC351320
TECLEAMINE
SCHEMBL31221605
DTXSID50233649
NSC 351320
NSC-351320
9-Methoxy-4-[(3-methylbut-2-en-1-yl)oxy]-2H-[1,3]dioxolo[4,5-g]furo[2,3-b]quinoline

2D Structure

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2D Structure of 1,3-Dioxolo(4,5-g)furo(2,3-b)quinoline, 9-methoxy-4-((3-methyl-2-butenyl)oxy)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 + 0.7335 73.35%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5508 55.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6600 66.00%
P-glycoprotein inhibitior - 0.4443 44.43%
P-glycoprotein substrate - 0.7304 73.04%
CYP3A4 substrate + 0.5256 52.56%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7610 76.10%
CYP3A4 inhibition + 0.8966 89.66%
CYP2C9 inhibition + 0.5400 54.00%
CYP2C19 inhibition + 0.5752 57.52%
CYP2D6 inhibition - 0.6932 69.32%
CYP1A2 inhibition + 0.7771 77.71%
CYP2C8 inhibition + 0.5297 52.97%
CYP inhibitory promiscuity + 0.9002 90.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5648 56.48%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.4935 49.35%
Skin irritation - 0.7957 79.57%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis + 0.6846 68.46%
Human Ether-a-go-go-Related Gene inhibition + 0.6795 67.95%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.7751 77.51%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.5694 56.94%
Acute Oral Toxicity (c) III 0.6631 66.31%
Estrogen receptor binding + 0.7084 70.84%
Androgen receptor binding + 0.6119 61.19%
Thyroid receptor binding + 0.7761 77.61%
Glucocorticoid receptor binding + 0.9037 90.37%
Aromatase binding + 0.7148 71.48%
PPAR gamma + 0.8361 83.61%
Honey bee toxicity - 0.8473 84.73%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8383 83.83%

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 98.08% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.12% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.87% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.55% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.32% 96.77%
CHEMBL3401 O75469 Pregnane X receptor 91.68% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.57% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.51% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.50% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.74% 86.33%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 87.64% 89.44%
CHEMBL5747 Q92793 CREB-binding protein 86.52% 95.12%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.51% 93.10%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.46% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.21% 95.56%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.73% 94.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.27% 99.23%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.58% 85.49%
CHEMBL2581 P07339 Cathepsin D 81.49% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.20% 96.67%
CHEMBL1937 Q92769 Histone deacetylase 2 81.04% 94.75%

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.
Vepris oubanguensis

Cross-Links

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PubChem 158686
LOTUS LTS0118312
wikiData Q83115261