Methylevoxine

Details

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Internal ID 877be136-3ef7-4afb-a1c6-161e9784aa21
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Furanoquinolines
IUPAC Name 1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methoxy-3-methylbutan-2-ol
SMILES (Canonical) CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)OC
SMILES (Isomeric) CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)OC
InChI InChI=1S/C19H23NO6/c1-19(2,24-5)14(21)10-26-13-7-6-11-15(17(13)23-4)20-18-12(8-9-25-18)16(11)22-3/h6-9,14,21H,10H2,1-5H3
InChI Key UPLMFBXLYYAFTF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO6
Molecular Weight 361.40 g/mol
Exact Mass 361.15253745 g/mol
Topological Polar Surface Area (TPSA) 83.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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56775-80-5
DTXSID601346497

2D Structure

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2D Structure of Methylevoxine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9735 97.35%
Caco-2 + 0.6845 68.45%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6101 61.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9079 90.79%
P-glycoprotein inhibitior - 0.7408 74.08%
P-glycoprotein substrate - 0.5681 56.81%
CYP3A4 substrate + 0.5465 54.65%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.6667 66.67%
CYP3A4 inhibition - 0.6434 64.34%
CYP2C9 inhibition - 0.8365 83.65%
CYP2C19 inhibition - 0.8215 82.15%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition + 0.8576 85.76%
CYP2C8 inhibition + 0.5721 57.21%
CYP inhibitory promiscuity - 0.6107 61.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5810 58.10%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9190 91.90%
Skin irritation - 0.8151 81.51%
Skin corrosion - 0.9440 94.40%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7499 74.99%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8250 82.50%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8313 83.13%
Acute Oral Toxicity (c) III 0.6155 61.55%
Estrogen receptor binding + 0.7986 79.86%
Androgen receptor binding + 0.6865 68.65%
Thyroid receptor binding + 0.8252 82.52%
Glucocorticoid receptor binding + 0.8874 88.74%
Aromatase binding + 0.7834 78.34%
PPAR gamma + 0.7760 77.60%
Honey bee toxicity - 0.8821 88.21%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.6624 66.24%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.33% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.59% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.50% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.42% 96.00%
CHEMBL5747 Q92793 CREB-binding protein 91.37% 95.12%
CHEMBL213 P08588 Beta-1 adrenergic receptor 88.04% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.76% 99.17%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.57% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 85.28% 94.73%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.56% 96.90%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.29% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.97% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.49% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.69% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.49% 93.65%
CHEMBL2581 P07339 Cathepsin D 80.48% 98.95%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.02% 94.03%

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.
Haplophyllum acutifolium
Haplophyllum obtusifolium
Haplophyllum ramosissimum

Cross-Links

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PubChem 3569287
LOTUS LTS0118277
wikiData Q104396871