Uvariopsine

Details

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Internal ID 735cad7a-c185-48db-b146-5980b67efef0
Taxonomy Alkaloids and derivatives > 6,6a-secoaporphines
IUPAC Name 2-(9-methoxynaphtho[2,1-g][1,3]benzodioxol-5-yl)-N,N-dimethylethanamine
SMILES (Canonical) CN(C)CCC1=CC2=C(C3=C1C=CC4=C3C=CC(=C4)OC)OCO2
SMILES (Isomeric) CN(C)CCC1=CC2=C(C3=C1C=CC4=C3C=CC(=C4)OC)OCO2
InChI InChI=1S/C20H21NO3/c1-21(2)9-8-14-11-18-20(24-12-23-18)19-16(14)6-4-13-10-15(22-3)5-7-17(13)19/h4-7,10-11H,8-9,12H2,1-3H3
InChI Key VOBOKMKHEYYRGG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO3
Molecular Weight 323.40 g/mol
Exact Mass 323.15214353 g/mol
Topological Polar Surface Area (TPSA) 30.90 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2-(9-methoxynaphtho[2,1-g][1,3]benzodioxol-5-yl)-N,N-dimethylethanamine

2D Structure

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2D Structure of Uvariopsine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.9098 90.98%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4750 47.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9238 92.38%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.8716 87.16%
P-glycoprotein inhibitior + 0.7935 79.35%
P-glycoprotein substrate - 0.5727 57.27%
CYP3A4 substrate + 0.5870 58.70%
CYP2C9 substrate - 0.6129 61.29%
CYP2D6 substrate + 0.7342 73.42%
CYP3A4 inhibition - 0.6686 66.86%
CYP2C9 inhibition - 0.6608 66.08%
CYP2C19 inhibition - 0.6914 69.14%
CYP2D6 inhibition + 0.9006 90.06%
CYP1A2 inhibition + 0.6182 61.82%
CYP2C8 inhibition - 0.7557 75.57%
CYP inhibitory promiscuity + 0.5402 54.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5422 54.22%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9161 91.61%
Skin irritation - 0.7728 77.28%
Skin corrosion - 0.9141 91.41%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8743 87.43%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8044 80.44%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8338 83.38%
Acute Oral Toxicity (c) III 0.5992 59.92%
Estrogen receptor binding + 0.8529 85.29%
Androgen receptor binding + 0.8069 80.69%
Thyroid receptor binding + 0.7879 78.79%
Glucocorticoid receptor binding + 0.6377 63.77%
Aromatase binding + 0.7105 71.05%
PPAR gamma + 0.6284 62.84%
Honey bee toxicity - 0.8246 82.46%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8451 84.51%

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
CHEMBL240 Q12809 HERG 99.38% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.80% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.39% 96.77%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.56% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.63% 92.62%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.54% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.28% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.66% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.77% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.98% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.75% 98.95%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 87.81% 80.96%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.09% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.77% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 85.15% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 84.68% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.63% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.63% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.30% 94.45%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.24% 96.67%
CHEMBL4581 P52732 Kinesin-like protein 1 80.29% 93.18%

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.
Uvariopsis tripetala

Cross-Links

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PubChem 13895191
LOTUS LTS0033899
wikiData Q105290086