Flavoserpentinine

Details

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Internal ID 6b4b0471-8477-4498-aef6-89bffe186dbb
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 3-ethylindolo[2,3-a]quinolizine
SMILES (Canonical) CCC1=CN2C=CC3=C4C=CC=CC4=NC3=C2C=C1
SMILES (Isomeric) CCC1=CN2C=CC3=C4C=CC=CC4=NC3=C2C=C1
InChI InChI=1S/C17H14N2/c1-2-12-7-8-16-17-14(9-10-19(16)11-12)13-5-3-4-6-15(13)18-17/h3-11H,2H2,1H3
InChI Key BAALMEGRQMMBJQ-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14N2
Molecular Weight 246.31 g/mol
Exact Mass 246.115698455 g/mol
Topological Polar Surface Area (TPSA) 17.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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12H-Indolo[2,3-a]quinolizin-5-ium, 3-ethyl-, inner salt
12h-indolo(2,3-a)quinolizin-5-ium, 3-ethyl-, inner salt
RefChem:197134
Flavopereirine [MI]
UNII-JIG1Q7Z9UH
SCHEMBL3093569
DTXSID401204778
3-Ethylindolo[2,3-a]quinolizin-5-ium-12-ide
Q27281519

2D Structure

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2D Structure of Flavoserpentinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.8605 86.05%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7366 73.66%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9251 92.51%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7069 70.69%
BSEP inhibitior + 0.8792 87.92%
P-glycoprotein inhibitior - 0.8228 82.28%
P-glycoprotein substrate - 0.7558 75.58%
CYP3A4 substrate + 0.5062 50.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7068 70.68%
CYP3A4 inhibition + 0.5077 50.77%
CYP2C9 inhibition - 0.7520 75.20%
CYP2C19 inhibition - 0.5727 57.27%
CYP2D6 inhibition + 0.5276 52.76%
CYP1A2 inhibition + 0.8562 85.62%
CYP2C8 inhibition + 0.8187 81.87%
CYP inhibitory promiscuity + 0.8441 84.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4974 49.74%
Eye corrosion - 0.9330 93.30%
Eye irritation - 0.7738 77.38%
Skin irritation - 0.5386 53.86%
Skin corrosion - 0.9344 93.44%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6849 68.49%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.7556 75.56%
skin sensitisation - 0.8160 81.60%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7441 74.41%
Acute Oral Toxicity (c) III 0.6870 68.70%
Estrogen receptor binding + 0.9785 97.85%
Androgen receptor binding + 0.8262 82.62%
Thyroid receptor binding + 0.8196 81.96%
Glucocorticoid receptor binding + 0.9083 90.83%
Aromatase binding + 0.9302 93.02%
PPAR gamma + 0.7748 77.48%
Honey bee toxicity - 0.9037 90.37%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity - 0.3711 37.11%

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
CHEMBL2581 P07339 Cathepsin D 96.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.96% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.04% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.81% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.11% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 89.31% 96.25%
CHEMBL240 Q12809 HERG 88.80% 89.76%
CHEMBL230 P35354 Cyclooxygenase-2 86.89% 89.63%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.88% 96.67%
CHEMBL1781 P11387 DNA topoisomerase I 85.12% 97.00%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 83.91% 87.50%
CHEMBL4237 O75582 Ribosomal protein S6 kinase alpha 5 83.10% 91.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 82.60% 89.44%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.52% 92.67%
CHEMBL1944 P08473 Neprilysin 81.07% 92.63%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.80% 93.81%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.67% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.05% 94.00%

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.
Geissospermum laeve
Geissospermum sericeum
Strychnos longicaudata

Cross-Links

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PubChem 10131104
LOTUS LTS0061383
wikiData Q27281519