Erythramine

Details

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Internal ID 08f4759b-2871-4a4f-975a-5a680fedf316
Taxonomy Alkaloids and derivatives > Erythrina alkaloids > Erythrinanes
IUPAC Name (1S,19S)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraene
SMILES (Canonical) COC1CC=C2CCN3C2(C1)C4=CC5=C(C=C4CC3)OCO5
SMILES (Isomeric) CO[C@H]1CC=C2CCN3[C@]2(C1)C4=CC5=C(C=C4CC3)OCO5
InChI InChI=1S/C18H21NO3/c1-20-14-3-2-13-5-7-19-6-4-12-8-16-17(22-11-21-16)9-15(12)18(13,19)10-14/h2,8-9,14H,3-7,10-11H2,1H3/t14-,18-/m0/s1
InChI Key UGJWEDNGBKKYSX-KSSFIOAISA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H21NO3
Molecular Weight 299.40 g/mol
Exact Mass 299.15214353 g/mol
Topological Polar Surface Area (TPSA) 30.90 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 4
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 Erythramine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9543 95.43%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6212 62.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9357 93.57%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8458 84.58%
P-glycoprotein inhibitior - 0.6557 65.57%
P-glycoprotein substrate - 0.7424 74.24%
CYP3A4 substrate + 0.5973 59.73%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.5702 57.02%
CYP3A4 inhibition - 0.6481 64.81%
CYP2C9 inhibition - 0.9082 90.82%
CYP2C19 inhibition - 0.7351 73.51%
CYP2D6 inhibition + 0.6973 69.73%
CYP1A2 inhibition - 0.6103 61.03%
CYP2C8 inhibition - 0.8192 81.92%
CYP inhibitory promiscuity + 0.5081 50.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5057 50.57%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9380 93.80%
Skin irritation - 0.7784 77.84%
Skin corrosion - 0.9270 92.70%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7961 79.61%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation - 0.7905 79.05%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.4939 49.39%
Acute Oral Toxicity (c) III 0.5211 52.11%
Estrogen receptor binding + 0.5852 58.52%
Androgen receptor binding + 0.6437 64.37%
Thyroid receptor binding + 0.6468 64.68%
Glucocorticoid receptor binding + 0.5411 54.11%
Aromatase binding - 0.5274 52.74%
PPAR gamma + 0.5904 59.04%
Honey bee toxicity - 0.7507 75.07%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.7972 79.72%

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 97.82% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.62% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.26% 94.45%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 95.70% 93.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.65% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.82% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.28% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.87% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.35% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.95% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.47% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.17% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.75% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.44% 95.56%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 83.94% 90.95%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.94% 90.24%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.80% 82.67%

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.
Erythrina fusca
Erythrina leptorhiza
Erythrina sandwicensis

Cross-Links

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PubChem 101289752
LOTUS LTS0266339
wikiData Q104254208