N-noratherosperminine

Details

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Internal ID 166d9ea5-9e14-4ab5-94d0-0dec9c04d729
Taxonomy Alkaloids and derivatives > 6,6a-secoaporphines
IUPAC Name 2-(3,4-dimethoxyphenanthren-1-yl)-N-methylethanamine
SMILES (Canonical) CNCCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC
SMILES (Isomeric) CNCCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC
InChI InChI=1S/C19H21NO2/c1-20-11-10-14-12-17(21-2)19(22-3)18-15-7-5-4-6-13(15)8-9-16(14)18/h4-9,12,20H,10-11H2,1-3H3
InChI Key BRMNMGRFCCRFNA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO2
Molecular Weight 295.40 g/mol
Exact Mass 295.157228913 g/mol
Topological Polar Surface Area (TPSA) 30.50 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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74606-53-4
Noratherosperminine
AKOS040763686

2D Structure

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2D Structure of N-noratherosperminine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9504 95.04%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5245 52.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7255 72.55%
P-glycoprotein inhibitior + 0.6083 60.83%
P-glycoprotein substrate + 0.5633 56.33%
CYP3A4 substrate + 0.5711 57.11%
CYP2C9 substrate - 0.5742 57.42%
CYP2D6 substrate + 0.8048 80.48%
CYP3A4 inhibition - 0.7697 76.97%
CYP2C9 inhibition - 0.9123 91.23%
CYP2C19 inhibition - 0.9019 90.19%
CYP2D6 inhibition + 0.6372 63.72%
CYP1A2 inhibition + 0.7474 74.74%
CYP2C8 inhibition + 0.7518 75.18%
CYP inhibitory promiscuity - 0.8350 83.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6811 68.11%
Eye corrosion - 0.9712 97.12%
Eye irritation - 0.9155 91.55%
Skin irritation - 0.5522 55.22%
Skin corrosion - 0.8270 82.70%
Ames mutagenesis + 0.8063 80.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8043 80.43%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7992 79.92%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8643 86.43%
Acute Oral Toxicity (c) II 0.5522 55.22%
Estrogen receptor binding + 0.7761 77.61%
Androgen receptor binding + 0.8105 81.05%
Thyroid receptor binding + 0.7866 78.66%
Glucocorticoid receptor binding + 0.7431 74.31%
Aromatase binding + 0.5762 57.62%
PPAR gamma + 0.6729 67.29%
Honey bee toxicity - 0.7957 79.57%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.6781 67.81%

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 99.04% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.15% 91.11%
CHEMBL1914 P06276 Butyrylcholinesterase 95.91% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 91.14% 90.20%
CHEMBL2535 P11166 Glucose transporter 90.54% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.26% 94.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 88.69% 95.83%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.47% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.46% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.45% 86.33%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 88.21% 94.67%
CHEMBL3959 P16083 Quinone reductase 2 87.94% 89.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.76% 92.62%
CHEMBL4302 P08183 P-glycoprotein 1 85.60% 92.98%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.82% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.32% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.77% 93.99%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.11% 96.67%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.74% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 81.49% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.97% 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.
Curcuma wenyujin
Ficus septica
Fissistigma glaucescens

Cross-Links

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PubChem 10957406
NPASS NPC252620
LOTUS LTS0247972
wikiData Q104944908