[(4R,12S,13R,14S,19R,21S)-11-acetyl-9-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-14-yl] acetate

Details

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Internal ID 6e5c85e6-ea2d-4990-8e4b-6937b1a9b661
Taxonomy Alkaloids and derivatives > Strychnos alkaloids
IUPAC Name [(4R,12S,13R,14S,19R,21S)-11-acetyl-9-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-14-yl] acetate
SMILES (Canonical) CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3OC(=O)C)C6=C1C(=C(C=C6)OC)O
SMILES (Isomeric) CC(=O)N1[C@H]2[C@H]3[C@H]4C[C@H]5[C@@]2(CCN5CC4=CCO[C@H]3OC(=O)C)C6=C1C(=C(C=C6)OC)O
InChI InChI=1S/C24H28N2O6/c1-12(27)26-20-16(4-5-17(30-3)21(20)29)24-7-8-25-11-14-6-9-31-23(32-13(2)28)19(22(24)26)15(14)10-18(24)25/h4-6,15,18-19,22-23,29H,7-11H2,1-3H3/t15-,18-,19+,22-,23-,24+/m0/s1
InChI Key WUSIMBJXHMBCII-ZKHBPZIFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H28N2O6
Molecular Weight 440.50 g/mol
Exact Mass 440.19473662 g/mol
Topological Polar Surface Area (TPSA) 88.50 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 7
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 [(4R,12S,13R,14S,19R,21S)-11-acetyl-9-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-14-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9201 92.01%
Caco-2 + 0.7449 74.49%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6771 67.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9033 90.33%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.7631 76.31%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7815 78.15%
P-glycoprotein inhibitior + 0.7343 73.43%
P-glycoprotein substrate + 0.6700 67.00%
CYP3A4 substrate + 0.6993 69.93%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7193 71.93%
CYP3A4 inhibition - 0.6421 64.21%
CYP2C9 inhibition - 0.8709 87.09%
CYP2C19 inhibition - 0.8843 88.43%
CYP2D6 inhibition - 0.9173 91.73%
CYP1A2 inhibition - 0.8829 88.29%
CYP2C8 inhibition + 0.6808 68.08%
CYP inhibitory promiscuity - 0.8958 89.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4774 47.74%
Eye corrosion - 0.9845 98.45%
Eye irritation - 0.9624 96.24%
Skin irritation - 0.7675 76.75%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6842 68.42%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8549 85.49%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.5866 58.66%
Acute Oral Toxicity (c) III 0.6314 63.14%
Estrogen receptor binding + 0.7641 76.41%
Androgen receptor binding + 0.7175 71.75%
Thyroid receptor binding - 0.6639 66.39%
Glucocorticoid receptor binding + 0.7233 72.33%
Aromatase binding + 0.5763 57.63%
PPAR gamma + 0.6709 67.09%
Honey bee toxicity - 0.7790 77.90%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5499 54.99%
Fish aquatic toxicity + 0.9548 95.48%

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 99.47% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.04% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.47% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.12% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.83% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 91.45% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.80% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.38% 95.89%
CHEMBL4208 P20618 Proteasome component C5 88.12% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.59% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.55% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.35% 90.71%
CHEMBL2581 P07339 Cathepsin D 85.23% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.72% 89.62%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 84.49% 92.29%
CHEMBL5028 O14672 ADAM10 82.98% 97.50%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.06% 94.42%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.78% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.45% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.36% 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.
Strychnos staudtii

Cross-Links

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PubChem 13994708
LOTUS LTS0098174
wikiData Q105313270