Lycorenine

Details

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Internal ID e94f1246-2611-4757-91b2-1c96cd9b724b
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Homolycorine-type amaryllidaceae alkaloids
IUPAC Name (5aR,7S,11bS,11cS)-9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indol-7-ol
SMILES (Canonical) CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)O)OC)OC
SMILES (Isomeric) CN1CCC2=CC[C@@H]3[C@H]([C@@H]21)C4=CC(=C(C=C4[C@H](O3)O)OC)OC
InChI InChI=1S/C18H23NO4/c1-19-7-6-10-4-5-13-16(17(10)19)11-8-14(21-2)15(22-3)9-12(11)18(20)23-13/h4,8-9,13,16-18,20H,5-7H2,1-3H3/t13-,16-,17-,18+/m1/s1
InChI Key VHYYSQODIQWPDO-PILAGYSTSA-N
Popularity 61 references in papers

Physical and Chemical Properties

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Molecular Formula C18H23NO4
Molecular Weight 317.40 g/mol
Exact Mass 317.16270821 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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477-19-0
Lycorenin
(5aR,7S,11bS,11cS)-9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indol-7-ol
(7alpha)-9,10-Dimethoxy-1-methyllycorenan-7-ol
CHEBI:6599
CHEMBL4208558
DTXSID20963901
HY-N6050
MFCD09954183
AKOS040750451
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lycorenine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9189 91.89%
Caco-2 + 0.8349 83.49%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6005 60.05%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9292 92.92%
OATP1B3 inhibitior + 0.9303 93.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.4878 48.78%
P-glycoprotein inhibitior - 0.7931 79.31%
P-glycoprotein substrate - 0.5193 51.93%
CYP3A4 substrate + 0.5687 56.87%
CYP2C9 substrate + 0.6075 60.75%
CYP2D6 substrate + 0.6868 68.68%
CYP3A4 inhibition - 0.8733 87.33%
CYP2C9 inhibition - 0.9194 91.94%
CYP2C19 inhibition - 0.8291 82.91%
CYP2D6 inhibition + 0.7060 70.60%
CYP1A2 inhibition - 0.6981 69.81%
CYP2C8 inhibition - 0.7614 76.14%
CYP inhibitory promiscuity - 0.8654 86.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5298 52.98%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9763 97.63%
Skin irritation - 0.7717 77.17%
Skin corrosion - 0.9385 93.85%
Ames mutagenesis - 0.5437 54.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6445 64.45%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8534 85.34%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6368 63.68%
Acute Oral Toxicity (c) III 0.5791 57.91%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5467 54.67%
Thyroid receptor binding + 0.6002 60.02%
Glucocorticoid receptor binding + 0.7261 72.61%
Aromatase binding - 0.6224 62.24%
PPAR gamma + 0.5773 57.73%
Honey bee toxicity - 0.8027 80.27%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9515 95.15%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.00% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.16% 85.14%
CHEMBL4208 P20618 Proteasome component C5 92.58% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.99% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.66% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.40% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.87% 93.40%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.61% 97.36%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.22% 89.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.96% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.66% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.28% 94.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.01% 90.24%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.02% 91.03%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.77% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.75% 90.71%

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.
Hymenocallis littoralis
Lycoris radiata
Narcissus munozii-garmendiae
Narcissus pseudonarcissus

Cross-Links

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PubChem 160472
LOTUS LTS0115054
wikiData Q27107263