Methyl 18-hydroxy-13-(1-hydroxyethyl)-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate

Details

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Internal ID 59d109c2-343a-4718-9a96-dbaa62de1031
Taxonomy Alkaloids and derivatives > Corynanthean-type alkaloids
IUPAC Name methyl 18-hydroxy-13-(1-hydroxyethyl)-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H28N2O4/c1-11(25)12-10-24-16-8-14(12)22(20(27)28-3)17(24)9-21(19(22)26)13-6-4-5-7-15(13)23(2)18(16)21/h4-7,11-12,14,16-19,25-26H,8-10H2,1-3H3
InChI Key OEGZONSWPCBTKS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28N2O4
Molecular Weight 384.50 g/mol
Exact Mass 384.20490738 g/mol
Topological Polar Surface Area (TPSA) 73.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 0.75
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 18-hydroxy-13-(1-hydroxyethyl)-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8051 80.51%
Caco-2 + 0.7402 74.02%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5288 52.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9080 90.80%
OATP1B3 inhibitior + 0.9231 92.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5123 51.23%
P-glycoprotein inhibitior - 0.6695 66.95%
P-glycoprotein substrate + 0.7009 70.09%
CYP3A4 substrate + 0.6934 69.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4782 47.82%
CYP3A4 inhibition - 0.9310 93.10%
CYP2C9 inhibition - 0.8762 87.62%
CYP2C19 inhibition - 0.8298 82.98%
CYP2D6 inhibition - 0.6923 69.23%
CYP1A2 inhibition - 0.8403 84.03%
CYP2C8 inhibition - 0.7506 75.06%
CYP inhibitory promiscuity - 0.8972 89.72%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6117 61.17%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9875 98.75%
Skin irritation - 0.7966 79.66%
Skin corrosion - 0.9470 94.70%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6572 65.72%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5060 50.60%
skin sensitisation - 0.8800 88.00%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7186 71.86%
Acute Oral Toxicity (c) III 0.4751 47.51%
Estrogen receptor binding + 0.7525 75.25%
Androgen receptor binding + 0.7052 70.52%
Thyroid receptor binding + 0.6559 65.59%
Glucocorticoid receptor binding - 0.4779 47.79%
Aromatase binding + 0.5278 52.78%
PPAR gamma - 0.5129 51.29%
Honey bee toxicity - 0.7947 79.47%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9601 96.01%

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 99.33% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.36% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.91% 85.14%
CHEMBL2535 P11166 Glucose transporter 92.49% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.61% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.09% 97.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.29% 93.56%
CHEMBL4208 P20618 Proteasome component C5 87.19% 90.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.05% 82.69%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.51% 94.62%
CHEMBL5028 O14672 ADAM10 86.15% 97.50%
CHEMBL221 P23219 Cyclooxygenase-1 85.37% 90.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.50% 96.47%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.39% 91.07%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.01% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.68% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.03% 100.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.88% 94.08%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.46% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.30% 96.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.97% 97.09%

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.
Alstonia macrophylla

Cross-Links

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PubChem 163009473
LOTUS LTS0159243
wikiData Q104888658