N,N-dimethyl-2-(3,4,8-trimethoxyphenanthren-1-yl)ethanamine

Details

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Internal ID d6ea7ba8-b113-4161-8257-fdaeca86d136
Taxonomy Alkaloids and derivatives > 6,6a-secoaporphines
IUPAC Name N,N-dimethyl-2-(3,4,8-trimethoxyphenanthren-1-yl)ethanamine
SMILES (Canonical) CN(C)CCC1=CC(=C(C2=C1C=CC3=C2C=CC=C3OC)OC)OC
SMILES (Isomeric) CN(C)CCC1=CC(=C(C2=C1C=CC3=C2C=CC=C3OC)OC)OC
InChI InChI=1S/C21H25NO3/c1-22(2)12-11-14-13-19(24-4)21(25-5)20-15(14)9-10-16-17(20)7-6-8-18(16)23-3/h6-10,13H,11-12H2,1-5H3
InChI Key BRVAMLXEJGKDSX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H25NO3
Molecular Weight 339.40 g/mol
Exact Mass 339.18344366 g/mol
Topological Polar Surface Area (TPSA) 30.90 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.12
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N,N-dimethyl-2-(3,4,8-trimethoxyphenanthren-1-yl)ethanamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.9569 95.69%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6750 67.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior + 0.8162 81.62%
P-glycoprotein inhibitior + 0.7060 70.60%
P-glycoprotein substrate + 0.5132 51.32%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.8602 86.02%
CYP3A4 inhibition - 0.7627 76.27%
CYP2C9 inhibition - 0.5252 52.52%
CYP2C19 inhibition - 0.8385 83.85%
CYP2D6 inhibition + 0.5558 55.58%
CYP1A2 inhibition + 0.7977 79.77%
CYP2C8 inhibition + 0.5268 52.68%
CYP inhibitory promiscuity - 0.7874 78.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6465 64.65%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8681 86.81%
Skin irritation - 0.7307 73.07%
Skin corrosion - 0.8752 87.52%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9297 92.97%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8526 85.26%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.9004 90.04%
Acute Oral Toxicity (c) III 0.4922 49.22%
Estrogen receptor binding + 0.7281 72.81%
Androgen receptor binding + 0.6613 66.13%
Thyroid receptor binding + 0.7300 73.00%
Glucocorticoid receptor binding + 0.7511 75.11%
Aromatase binding + 0.8096 80.96%
PPAR gamma - 0.4849 48.49%
Honey bee toxicity - 0.7569 75.69%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9304 93.04%

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 97.97% 89.76%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.58% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.38% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.18% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.91% 95.56%
CHEMBL2535 P11166 Glucose transporter 92.18% 98.75%
CHEMBL2581 P07339 Cathepsin D 91.90% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.12% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 90.23% 90.20%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 89.59% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.19% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.03% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.82% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.45% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 85.03% 93.31%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.87% 96.67%
CHEMBL1914 P06276 Butyrylcholinesterase 84.41% 95.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.32% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.17% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 80.15% 94.73%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.04% 95.48%

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.
Fissistigma glaucescens

Cross-Links

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PubChem 14635657
LOTUS LTS0157316
wikiData Q104945032