methoxy-xanthocillin X dimethylether

Details

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Internal ID fc4807d3-fb65-4d20-8617-3fd3bc40e0cb
IUPAC Name 4-[(1Z,3Z)-2,3-diisocyano-4-(4-methoxyphenyl)buta-1,3-dienyl]-1,2-dimethoxybenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18N2O3/c1-22-18(12-15-6-9-17(24-3)10-7-15)19(23-2)13-16-8-11-20(25-4)21(14-16)26-5/h6-14H,3-5H3/b18-12-,19-13-
InChI Key GTCYCSHLUXYSAO-BKHHGCLFSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18N2O3
Molecular Weight 346.40 g/mol
Exact Mass 346.13174244 g/mol
Topological Polar Surface Area (TPSA) 36.40 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.93
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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methoxy-xanthocillin X dimethylether

2D Structure

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2D Structure of methoxy-xanthocillin X dimethylether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.6101 61.01%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6516 65.16%
OATP2B1 inhibitior - 0.7137 71.37%
OATP1B1 inhibitior + 0.9386 93.86%
OATP1B3 inhibitior + 0.9594 95.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9235 92.35%
P-glycoprotein inhibitior + 0.6508 65.08%
P-glycoprotein substrate - 0.8849 88.49%
CYP3A4 substrate - 0.5500 55.00%
CYP2C9 substrate - 0.8200 82.00%
CYP2D6 substrate - 0.7866 78.66%
CYP3A4 inhibition + 0.8607 86.07%
CYP2C9 inhibition - 0.7725 77.25%
CYP2C19 inhibition - 0.5377 53.77%
CYP2D6 inhibition - 0.8942 89.42%
CYP1A2 inhibition + 0.7823 78.23%
CYP2C8 inhibition + 0.4932 49.32%
CYP inhibitory promiscuity + 0.9110 91.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7431 74.31%
Carcinogenicity (trinary) Danger 0.3849 38.49%
Eye corrosion - 0.9779 97.79%
Eye irritation - 0.5450 54.50%
Skin irritation - 0.8385 83.85%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8828 88.28%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.5789 57.89%
skin sensitisation - 0.8663 86.63%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6474 64.74%
Acute Oral Toxicity (c) III 0.5339 53.39%
Estrogen receptor binding + 0.9001 90.01%
Androgen receptor binding + 0.6636 66.36%
Thyroid receptor binding + 0.8388 83.88%
Glucocorticoid receptor binding + 0.7587 75.87%
Aromatase binding + 0.6881 68.81%
PPAR gamma + 0.7555 75.55%
Honey bee toxicity - 0.9477 94.77%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9625 96.25%

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
CHEMBL4208 P20618 Proteasome component C5 93.06% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.68% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.55% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.57% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.51% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 86.70% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.35% 96.09%
CHEMBL2535 P11166 Glucose transporter 85.91% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.65% 99.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.57% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.33% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.94% 95.89%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.66% 90.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 59594915
LOTUS LTS0189937
wikiData Q77372646