(-)-N-nornuciferine

Details

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Internal ID d8ba5b97-fd07-4fb4-b52b-b83578147f61
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
SMILES (Canonical) COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC
SMILES (Isomeric) COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC
InChI InChI=1S/C18H19NO2/c1-20-15-10-12-7-8-19-14-9-11-5-3-4-6-13(11)17(16(12)14)18(15)21-2/h3-6,10,14,19H,7-9H2,1-2H3
InChI Key QQKAHDMMPBQDAC-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C18H19NO2
Molecular Weight 281.30 g/mol
Exact Mass 281.141578849 g/mol
Topological Polar Surface Area (TPSA) 30.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEMBL36496
ACon1_001877
AKOS037514752
NCGC00180048-01
FT-0775684

2D Structure

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2D Structure of (-)-N-nornuciferine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9333 93.33%
Blood Brain Barrier + 0.9129 91.29%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6148 61.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.6314 63.14%
P-glycoprotein inhibitior - 0.7372 73.72%
P-glycoprotein substrate - 0.5935 59.35%
CYP3A4 substrate + 0.5985 59.85%
CYP2C9 substrate - 0.6489 64.89%
CYP2D6 substrate + 0.8137 81.37%
CYP3A4 inhibition - 0.7542 75.42%
CYP2C9 inhibition - 0.9230 92.30%
CYP2C19 inhibition - 0.8547 85.47%
CYP2D6 inhibition + 0.6857 68.57%
CYP1A2 inhibition + 0.5221 52.21%
CYP2C8 inhibition + 0.6019 60.19%
CYP inhibitory promiscuity - 0.7345 73.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7115 71.15%
Eye corrosion - 0.9742 97.42%
Eye irritation - 0.9849 98.49%
Skin irritation - 0.5995 59.95%
Skin corrosion - 0.8919 89.19%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8641 86.41%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8799 87.99%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7358 73.58%
Acute Oral Toxicity (c) II 0.5643 56.43%
Estrogen receptor binding - 0.5171 51.71%
Androgen receptor binding + 0.7133 71.33%
Thyroid receptor binding + 0.7415 74.15%
Glucocorticoid receptor binding + 0.5976 59.76%
Aromatase binding - 0.6529 65.29%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8455 84.55%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity - 0.6471 64.71%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4806 Q14761 Protein tyrosine phosphatase receptor type C-associated protein 5300 nM
IC50
DOI: 10.1016/0960-894X(95)00250-W

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.88% 91.11%
CHEMBL2535 P11166 Glucose transporter 92.57% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.62% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.16% 97.09%
CHEMBL2056 P21728 Dopamine D1 receptor 91.04% 91.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.40% 93.99%
CHEMBL2581 P07339 Cathepsin D 90.28% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.58% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.34% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 86.16% 95.62%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.01% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.65% 96.95%
CHEMBL1951 P21397 Monoamine oxidase A 84.60% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.38% 95.89%
CHEMBL4208 P20618 Proteasome component C5 84.03% 90.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.68% 94.03%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 82.28% 95.55%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.81% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.15% 94.00%

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.
Annickia polycarpa
Annona glabra
Annona muricata
Artabotrys hexapetalus
Chelonanthus albus
Guatteria blepharophylla
Hexalobus crispiflorus
Liriodendron tulipifera
Magnolia grandiflora
Magnolia obovata
Magnolia officinalis
Nelumbo lutea
Nelumbo nucifera
Piptostigma fugax

Cross-Links

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PubChem 624491
NPASS NPC126519
ChEMBL CHEMBL36496
LOTUS LTS0034266
wikiData Q105225883