Lycoranine A

Details

Top
Internal ID 0eb33fcb-baba-4498-9137-adcb5425e8c3
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Phenanthridines and derivatives
IUPAC Name 17-methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(19),2,4(8),9,13,15,17-heptaen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H11NO4/c1-20-10-4-9-2-3-18-16(9)12(5-10)11-6-14-15(22-8-21-14)7-13(11)17(18)19/h2-7H,8H2,1H3
InChI Key TUSUUFQLFKJKJW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H11NO4
Molecular Weight 293.27 g/mol
Exact Mass 293.06880783 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Lycoranine A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 + 0.9035 90.35%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4534 45.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9471 94.71%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9348 93.48%
BSEP inhibitior + 0.7358 73.58%
P-glycoprotein inhibitior - 0.6036 60.36%
P-glycoprotein substrate - 0.8883 88.83%
CYP3A4 substrate - 0.5205 52.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8411 84.11%
CYP3A4 inhibition + 0.8652 86.52%
CYP2C9 inhibition - 0.6793 67.93%
CYP2C19 inhibition + 0.5368 53.68%
CYP2D6 inhibition - 0.5993 59.93%
CYP1A2 inhibition + 0.9153 91.53%
CYP2C8 inhibition - 0.8806 88.06%
CYP inhibitory promiscuity + 0.8311 83.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4630 46.30%
Eye corrosion - 0.9833 98.33%
Eye irritation - 0.6585 65.85%
Skin irritation - 0.7917 79.17%
Skin corrosion - 0.9533 95.33%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5750 57.50%
Micronuclear + 0.7574 75.74%
Hepatotoxicity + 0.5823 58.23%
skin sensitisation - 0.8191 81.91%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5419 54.19%
Acute Oral Toxicity (c) III 0.6679 66.79%
Estrogen receptor binding + 0.9355 93.55%
Androgen receptor binding + 0.5748 57.48%
Thyroid receptor binding + 0.7502 75.02%
Glucocorticoid receptor binding + 0.8930 89.30%
Aromatase binding + 0.8623 86.23%
PPAR gamma + 0.6406 64.06%
Honey bee toxicity - 0.8680 86.80%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity - 0.3814 38.14%

Targets

Top

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.88% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.24% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.82% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.80% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.84% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.73% 93.99%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.61% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.18% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.69% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.51% 95.56%
CHEMBL4208 P20618 Proteasome component C5 87.82% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.46% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.28% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.28% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.85% 93.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.06% 99.23%

Plants that contains it

Top
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.
Lycoris radiata

Cross-Links

Top
PubChem 44130139
LOTUS LTS0045441
wikiData Q105265019