Goniomitine

Details

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Internal ID 189e7ad6-8e2c-4eea-a338-85341776cda9
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Naphthyridines
IUPAC Name 2-[(4aR,12aS)-4a-ethyl-2,3,4,5,6,12a-hexahydro-1H-indolo[1,2-a][1,8]naphthyridin-7-yl]ethanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H26N2O/c1-2-19-10-5-12-20-18(19)21-16-7-4-3-6-14(16)15(9-13-22)17(21)8-11-19/h3-4,6-7,18,20,22H,2,5,8-13H2,1H3/t18-,19+/m0/s1
InChI Key CGWKMDYVWRDDRF-RBUKOAKNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H26N2O
Molecular Weight 298.40 g/mol
Exact Mass 298.204513457 g/mol
Topological Polar Surface Area (TPSA) 37.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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SCHEMBL30832987
CHEBI:141908
2-[(4aR,12aS)-4a-ethyl-2,3,4,5,6,12a-hexahydro-1H-indolo[1,2-a][1,8]naphthyridin-7-yl]ethanol

2D Structure

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2D Structure of Goniomitine

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 + 0.8814 88.14%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.6782 67.82%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8464 84.64%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.8612 86.12%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.7094 70.94%
P-glycoprotein inhibitior - 0.7590 75.90%
P-glycoprotein substrate + 0.5420 54.20%
CYP3A4 substrate + 0.5943 59.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7106 71.06%
CYP3A4 inhibition - 0.7222 72.22%
CYP2C9 inhibition - 0.8885 88.85%
CYP2C19 inhibition - 0.7845 78.45%
CYP2D6 inhibition - 0.6189 61.89%
CYP1A2 inhibition - 0.7987 79.87%
CYP2C8 inhibition - 0.6302 63.02%
CYP inhibitory promiscuity - 0.7524 75.24%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6498 64.98%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.9833 98.33%
Skin irritation - 0.7677 76.77%
Skin corrosion - 0.8887 88.87%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8367 83.67%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5340 53.40%
skin sensitisation - 0.8588 85.88%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.9268 92.68%
Acute Oral Toxicity (c) III 0.6600 66.00%
Estrogen receptor binding + 0.5885 58.85%
Androgen receptor binding - 0.5084 50.84%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding - 0.4863 48.63%
Aromatase binding - 0.6280 62.80%
PPAR gamma + 0.7772 77.72%
Honey bee toxicity - 0.9314 93.14%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.5212 52.12%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.24% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.52% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.66% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.37% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.19% 93.99%
CHEMBL230 P35354 Cyclooxygenase-2 90.48% 89.63%
CHEMBL1937 Q92769 Histone deacetylase 2 90.05% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.70% 91.11%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 89.00% 90.71%
CHEMBL1914 P06276 Butyrylcholinesterase 88.50% 95.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 88.42% 96.25%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 87.85% 95.83%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.56% 90.08%
CHEMBL255 P29275 Adenosine A2b receptor 85.49% 98.59%
CHEMBL228 P31645 Serotonin transporter 84.79% 95.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.56% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.70% 89.00%
CHEMBL5028 O14672 ADAM10 82.61% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.26% 92.62%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.00% 96.39%

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.
Gonioma malagasy

Cross-Links

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PubChem 24767757
LOTUS LTS0154256
wikiData Q104958314