Lycoranine B

Details

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Internal ID a266218f-79e6-457e-9f72-e42c4de5a4e4
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Phenanthridines and derivatives
IUPAC Name 17-methoxy-13-methyl-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) CC1=CC2=CC(=CC3=C2N1C(=O)C4=CC5=C(C=C43)OCO5)OC
SMILES (Isomeric) CC1=CC2=CC(=CC3=C2N1C(=O)C4=CC5=C(C=C43)OCO5)OC
InChI InChI=1S/C18H13NO4/c1-9-3-10-4-11(21-2)5-13-12-6-15-16(23-8-22-15)7-14(12)18(20)19(9)17(10)13/h3-7H,8H2,1-2H3
InChI Key VNGXAACSTLPKAN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H13NO4
Molecular Weight 307.30 g/mol
Exact Mass 307.08445790 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lycoranine B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 + 0.9339 93.39%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4131 41.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9348 93.48%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9598 95.98%
BSEP inhibitior + 0.7028 70.28%
P-glycoprotein inhibitior - 0.5855 58.55%
P-glycoprotein substrate - 0.8962 89.62%
CYP3A4 substrate - 0.5228 52.28%
CYP2C9 substrate - 0.7847 78.47%
CYP2D6 substrate - 0.8781 87.81%
CYP3A4 inhibition + 0.8566 85.66%
CYP2C9 inhibition - 0.6363 63.63%
CYP2C19 inhibition + 0.5511 55.11%
CYP2D6 inhibition - 0.6506 65.06%
CYP1A2 inhibition + 0.9053 90.53%
CYP2C8 inhibition - 0.9087 90.87%
CYP inhibitory promiscuity + 0.8520 85.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5084 50.84%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.5596 55.96%
Skin irritation - 0.8033 80.33%
Skin corrosion - 0.9572 95.72%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7474 74.74%
Hepatotoxicity + 0.5698 56.98%
skin sensitisation - 0.8319 83.19%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5338 53.38%
Acute Oral Toxicity (c) III 0.6225 62.25%
Estrogen receptor binding + 0.8954 89.54%
Androgen receptor binding + 0.5531 55.31%
Thyroid receptor binding + 0.7216 72.16%
Glucocorticoid receptor binding + 0.8918 89.18%
Aromatase binding + 0.8035 80.35%
PPAR gamma + 0.5603 56.03%
Honey bee toxicity - 0.8465 84.65%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.6596 65.96%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.38% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.14% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.36% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.84% 93.99%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.63% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.06% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.46% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.11% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.43% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.30% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.46% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.51% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.81% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.89% 89.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.35% 86.00%

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.
Coptis chinensis
Coptis deltoidea
Coptis japonica
Coptis teeta
Lycoris radiata

Cross-Links

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PubChem 44130138
NPASS NPC243044
LOTUS LTS0001774
wikiData Q105289614