(1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-11-one

Details

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Internal ID 199631cd-a8a9-42fc-bc5e-c9dab53b8082
Taxonomy Alkaloids and derivatives > Ibogan-type alkaloids
IUPAC Name (1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24N2O2/c1-3-12-6-11-7-15-19-18(17(23)10-22(9-11)20(12)15)14-8-13(24-2)4-5-16(14)21-19/h4-5,8,11-12,15,20-21H,3,6-7,9-10H2,1-2H3/t11-,12-,15-,20-/m0/s1
InChI Key KQABPFRLIMUVDP-CFOBNSSQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24N2O2
Molecular Weight 324.40 g/mol
Exact Mass 324.183778013 g/mol
Topological Polar Surface Area (TPSA) 45.30 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,15S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-11-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8032 80.32%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5938 59.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.6633 66.33%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.9159 91.59%
P-glycoprotein inhibitior - 0.6250 62.50%
P-glycoprotein substrate + 0.6691 66.91%
CYP3A4 substrate + 0.6147 61.47%
CYP2C9 substrate + 0.8046 80.46%
CYP2D6 substrate + 0.3606 36.06%
CYP3A4 inhibition + 0.6046 60.46%
CYP2C9 inhibition - 0.5169 51.69%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.6337 63.37%
CYP1A2 inhibition - 0.5529 55.29%
CYP2C8 inhibition - 0.6403 64.03%
CYP inhibitory promiscuity + 0.7002 70.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6191 61.91%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9334 93.34%
Skin irritation - 0.8017 80.17%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9168 91.68%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8782 87.82%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6269 62.69%
Acute Oral Toxicity (c) III 0.4668 46.68%
Estrogen receptor binding + 0.6010 60.10%
Androgen receptor binding + 0.8064 80.64%
Thyroid receptor binding - 0.5217 52.17%
Glucocorticoid receptor binding + 0.6990 69.90%
Aromatase binding + 0.7097 70.97%
PPAR gamma - 0.5737 57.37%
Honey bee toxicity - 0.8504 85.04%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.4388 43.88%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.38% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.10% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.19% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.77% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 95.65% 93.31%
CHEMBL255 P29275 Adenosine A2b receptor 95.15% 98.59%
CHEMBL2581 P07339 Cathepsin D 94.64% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.49% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.36% 93.99%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.11% 86.92%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.43% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.55% 92.94%
CHEMBL2535 P11166 Glucose transporter 87.35% 98.75%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.47% 92.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.45% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.80% 94.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.60% 96.77%
CHEMBL1781 P11387 DNA topoisomerase I 82.97% 97.00%
CHEMBL4208 P20618 Proteasome component C5 81.77% 90.00%
CHEMBL4805 Q99572 P2X purinoceptor 7 81.56% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.57% 92.62%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.42% 97.21%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.41% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.18% 97.14%

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.
Tabernaemontana corymbosa

Cross-Links

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PubChem 122179182
LOTUS LTS0096451
wikiData Q105144433