Apateline

Details

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Internal ID d7c2cecc-4b2f-4c41-8b8f-7d563606962e
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (8R,21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol
SMILES (Canonical) CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC
SMILES (Isomeric) CN1CCC2=CC(=C3C4=C2[C@@H]1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)C[C@@H]7C8=CC(=C(O3)C=C8CCN7)O4)O)OC
InChI InChI=1S/C34H32N2O5/c1-36-12-10-22-17-31(38-2)33-34-32(22)26(36)14-19-3-6-23(7-4-19)39-28-15-20(5-8-27(28)37)13-25-24-18-30(41-34)29(40-33)16-21(24)9-11-35-25/h3-8,15-18,25-26,35,37H,9-14H2,1-2H3/t25-,26+/m1/s1
InChI Key AFGMWONXXNDGGE-FTJBHMTQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H32N2O5
Molecular Weight 548.60 g/mol
Exact Mass 548.23112213 g/mol
Topological Polar Surface Area (TPSA) 72.40 Ų
XlogP 5.50
Atomic LogP (AlogP) 6.61
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEBI:182871
(8R,21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol

2D Structure

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2D Structure of Apateline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8631 86.31%
Caco-2 + 0.4946 49.46%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.7287 72.87%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.9304 93.04%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9919 99.19%
P-glycoprotein inhibitior + 0.9397 93.97%
P-glycoprotein substrate + 0.6893 68.93%
CYP3A4 substrate + 0.6869 68.69%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.7102 71.02%
CYP3A4 inhibition - 0.9736 97.36%
CYP2C9 inhibition - 0.9607 96.07%
CYP2C19 inhibition - 0.9234 92.34%
CYP2D6 inhibition - 0.9157 91.57%
CYP1A2 inhibition - 0.8822 88.22%
CYP2C8 inhibition + 0.4843 48.43%
CYP inhibitory promiscuity - 0.9802 98.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6863 68.63%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.9674 96.74%
Skin irritation - 0.7555 75.55%
Skin corrosion - 0.9418 94.18%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8718 87.18%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.8875 88.75%
skin sensitisation - 0.8700 87.00%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6967 69.67%
Acute Oral Toxicity (c) III 0.5979 59.79%
Estrogen receptor binding + 0.7283 72.83%
Androgen receptor binding + 0.7288 72.88%
Thyroid receptor binding + 0.5976 59.76%
Glucocorticoid receptor binding + 0.7944 79.44%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7065 70.65%
Honey bee toxicity - 0.7289 72.89%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.4343 43.43%

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 99.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.27% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.21% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.18% 93.99%
CHEMBL217 P14416 Dopamine D2 receptor 94.17% 95.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.97% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.91% 85.14%
CHEMBL2056 P21728 Dopamine D1 receptor 92.66% 91.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.60% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.15% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.21% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.89% 91.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.02% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.11% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.09% 86.33%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 85.00% 90.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.56% 89.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.47% 89.50%
CHEMBL4208 P20618 Proteasome component C5 84.41% 90.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.21% 92.94%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.82% 93.40%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.75% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.38% 99.23%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 80.41% 85.00%

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.
Cocculus pendulus
Daphnandra apatela
Guatteria guianensis
Pachygone loyaltiensis

Cross-Links

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PubChem 15560531
LOTUS LTS0024911
wikiData Q104911181