Dysoxyline

Details

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Internal ID 795948a1-9cbd-4681-a402-29226c214cc7
Taxonomy Organoheterocyclic compounds > Tetrahydroisoquinolines
IUPAC Name (1R)-1-[2-(1,3-benzodioxol-5-yl)ethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H25NO4/c1-22-9-8-15-11-19(23-2)20(24-3)12-16(15)17(22)6-4-14-5-7-18-21(10-14)26-13-25-18/h5,7,10-12,17H,4,6,8-9,13H2,1-3H3/t17-/m1/s1
InChI Key AGCGPVWWLORMQV-QGZVFWFLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H25NO4
Molecular Weight 355.40 g/mol
Exact Mass 355.17835828 g/mol
Topological Polar Surface Area (TPSA) 40.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL519734

2D Structure

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2D Structure of Dysoxyline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9029 90.29%
Caco-2 + 0.9394 93.94%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4414 44.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.9223 92.23%
P-glycoprotein inhibitior + 0.9512 95.12%
P-glycoprotein substrate + 0.5348 53.48%
CYP3A4 substrate + 0.6470 64.70%
CYP2C9 substrate - 0.6129 61.29%
CYP2D6 substrate + 0.7342 73.42%
CYP3A4 inhibition + 0.6526 65.26%
CYP2C9 inhibition - 0.8768 87.68%
CYP2C19 inhibition + 0.5291 52.91%
CYP2D6 inhibition + 0.7529 75.29%
CYP1A2 inhibition - 0.7357 73.57%
CYP2C8 inhibition - 0.7069 70.69%
CYP inhibitory promiscuity + 0.5339 53.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5964 59.64%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9864 98.64%
Skin irritation - 0.8135 81.35%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9315 93.15%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8759 87.59%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8263 82.63%
Acute Oral Toxicity (c) III 0.7426 74.26%
Estrogen receptor binding + 0.5926 59.26%
Androgen receptor binding - 0.5166 51.66%
Thyroid receptor binding + 0.6574 65.74%
Glucocorticoid receptor binding + 0.6813 68.13%
Aromatase binding - 0.7070 70.70%
PPAR gamma - 0.6619 66.19%
Honey bee toxicity - 0.7798 77.98%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9407 94.07%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.51% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.29% 96.77%
CHEMBL2581 P07339 Cathepsin D 95.89% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.84% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.63% 85.14%
CHEMBL261 P00915 Carbonic anhydrase I 95.52% 96.76%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.16% 93.40%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.05% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.67% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.65% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.19% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.10% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.73% 95.17%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 89.52% 90.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.79% 93.99%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.77% 95.78%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.25% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.75% 95.56%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.64% 89.50%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 83.46% 82.67%
CHEMBL2535 P11166 Glucose transporter 83.28% 98.75%
CHEMBL5555 O00767 Acyl-CoA desaturase 83.22% 97.50%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 82.75% 91.43%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.31% 99.17%
CHEMBL4208 P20618 Proteasome component C5 81.48% 90.00%
CHEMBL5747 Q92793 CREB-binding protein 81.36% 95.12%

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.
Didymocheton lenticellare

Cross-Links

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PubChem 44559821
LOTUS LTS0159560
wikiData Q104397580