Erysopine

Details

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Internal ID bf7ba65b-ffa6-4c76-9eca-81784e5a0857
Taxonomy Alkaloids and derivatives > Erythrina alkaloids > Erythrinanes
IUPAC Name 2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-11,12-diol
SMILES (Canonical) COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)O)C=C1
SMILES (Isomeric) COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)O)C=C1
InChI InChI=1S/C17H19NO3/c1-21-13-3-2-12-5-7-18-6-4-11-8-15(19)16(20)9-14(11)17(12,18)10-13/h2-3,5,8-9,13,19-20H,4,6-7,10H2,1H3
InChI Key GNBQGLMYBIWCOO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO3
Molecular Weight 285.34 g/mol
Exact Mass 285.13649347 g/mol
Topological Polar Surface Area (TPSA) 52.90 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Erysopine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9787 97.87%
Caco-2 + 0.8077 80.77%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8125 81.25%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.6517 65.17%
P-glycoprotein inhibitior - 0.8974 89.74%
P-glycoprotein substrate - 0.6022 60.22%
CYP3A4 substrate + 0.6064 60.64%
CYP2C9 substrate + 0.5925 59.25%
CYP2D6 substrate + 0.5274 52.74%
CYP3A4 inhibition - 0.9419 94.19%
CYP2C9 inhibition - 0.8591 85.91%
CYP2C19 inhibition - 0.7510 75.10%
CYP2D6 inhibition + 0.5504 55.04%
CYP1A2 inhibition - 0.6209 62.09%
CYP2C8 inhibition - 0.7957 79.57%
CYP inhibitory promiscuity - 0.7974 79.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5264 52.64%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8731 87.31%
Skin irritation - 0.7398 73.98%
Skin corrosion - 0.9203 92.03%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5263 52.63%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8190 81.90%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.7776 77.76%
Acute Oral Toxicity (c) III 0.4616 46.16%
Estrogen receptor binding + 0.6629 66.29%
Androgen receptor binding + 0.5686 56.86%
Thyroid receptor binding + 0.7150 71.50%
Glucocorticoid receptor binding + 0.7485 74.85%
Aromatase binding + 0.5376 53.76%
PPAR gamma + 0.6280 62.80%
Honey bee toxicity - 0.8195 81.95%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.7945 79.45%

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 98.33% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.39% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.39% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.55% 94.45%
CHEMBL4208 P20618 Proteasome component C5 89.72% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.24% 95.89%
CHEMBL2581 P07339 Cathepsin D 88.07% 98.95%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 87.25% 91.03%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.30% 93.40%
CHEMBL217 P14416 Dopamine D2 receptor 84.98% 95.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.18% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.39% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.07% 100.00%

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.
Erythrina berteroana
Erythrina fusca
Erythrina variegata

Cross-Links

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PubChem 12308892
LOTUS LTS0242537
wikiData Q105012278