Vasconine

Details

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Internal ID 0afa0632-fffb-472e-8778-3813325e7f29
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Phenanthridines and derivatives
IUPAC Name 4,5-dimethoxy-9-azoniatetracyclo[7.6.1.02,7.012,16]hexadeca-1(15),2,4,6,8,12(16),13-heptaene
SMILES (Canonical) COC1=C(C=C2C3=CC=CC4=C3[N+](=CC2=C1)CC4)OC
SMILES (Isomeric) COC1=C(C=C2C3=CC=CC4=C3[N+](=CC2=C1)CC4)OC
InChI InChI=1S/C17H16NO2/c1-19-15-8-12-10-18-7-6-11-4-3-5-13(17(11)18)14(12)9-16(15)20-2/h3-5,8-10H,6-7H2,1-2H3/q+1
InChI Key DYLVVAHQPYKZRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16NO2+
Molecular Weight 266.31 g/mol
Exact Mass 266.118103753 g/mol
Topological Polar Surface Area (TPSA) 22.30 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEBI:32290
C12188
AC1L9F0H
CHEMBL3306558
DYLVVAHQPYKZRX-UHFFFAOYSA-N
Q27114857
9,10-Dimethoxy-4,5-dihydropyrrolo[3,2,1-de]phenanthridin-6-ium
Pyrrolo[3,2,1-de]phenanthridinium, 4,5-dihydro-9,10-dimethoxy-
4,5-dimethoxy-9-azoniatetracyclo[7.6.1.02,7.012,16]hexadeca-1(15),2,4,6,8,12(16),13-heptaene

2D Structure

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2D Structure of Vasconine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9541 95.41%
Caco-2 + 0.9682 96.82%
Blood Brain Barrier + 0.8879 88.79%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.7223 72.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9453 94.53%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior + 0.7152 71.52%
BSEP inhibitior + 0.5769 57.69%
P-glycoprotein inhibitior - 0.7293 72.93%
P-glycoprotein substrate - 0.7467 74.67%
CYP3A4 substrate + 0.5530 55.30%
CYP2C9 substrate - 0.8233 82.33%
CYP2D6 substrate + 0.3791 37.91%
CYP3A4 inhibition - 0.7075 70.75%
CYP2C9 inhibition - 0.7168 71.68%
CYP2C19 inhibition - 0.6284 62.84%
CYP2D6 inhibition + 0.8331 83.31%
CYP1A2 inhibition + 0.7796 77.96%
CYP2C8 inhibition - 0.6559 65.59%
CYP inhibitory promiscuity + 0.7815 78.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5318 53.18%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.7525 75.25%
Skin irritation - 0.7307 73.07%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6885 68.85%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8897 88.97%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8277 82.77%
Acute Oral Toxicity (c) II 0.4990 49.90%
Estrogen receptor binding + 0.8187 81.87%
Androgen receptor binding + 0.6536 65.36%
Thyroid receptor binding + 0.7337 73.37%
Glucocorticoid receptor binding + 0.7625 76.25%
Aromatase binding + 0.5780 57.80%
PPAR gamma - 0.7095 70.95%
Honey bee toxicity - 0.8940 89.40%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity - 0.7595 75.95%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.30% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.57% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.75% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.35% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.19% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.37% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.07% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.85% 96.09%
CHEMBL2056 P21728 Dopamine D1 receptor 86.41% 91.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 86.31% 92.38%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.95% 94.03%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 85.94% 94.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.33% 92.62%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 81.76% 96.39%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.57% 100.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.50% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.51% 95.89%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.33% 92.67%

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.
Narcissus poeticus subsp. radiiflorus
Narcissus pseudonarcissus subsp. minor
Narcissus pseudonarcissus subsp. moschatus

Cross-Links

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PubChem 443690
LOTUS LTS0212704
wikiData Q27114857