[18,21,22,24-Tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] 1-methyl-6-oxopyridine-3-carboxylate

Details

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Internal ID aa456de5-6ced-4f19-993f-614e0bea3444
Taxonomy Alkaloids and derivatives
IUPAC Name [18,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] 1-methyl-6-oxopyridine-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C43H50N2O19/c1-19-20(2)37(52)62-34-32(59-23(5)48)36(63-38(53)26-13-14-28(51)45(10)16-26)42(18-56-21(3)46)35(61-25(7)50)31(58-22(4)47)29-33(60-24(6)49)43(42,41(34,9)55)64-40(29,8)17-57-39(54)27-12-11-15-44-30(19)27/h11-16,19-20,29,31-36,55H,17-18H2,1-10H3
InChI Key XORHGUAWVKAJST-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C43H50N2O19
Molecular Weight 898.90 g/mol
Exact Mass 898.30077737 g/mol
Topological Polar Surface Area (TPSA) 273.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 21
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [18,21,22,24-Tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] 1-methyl-6-oxopyridine-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5512 55.12%
Caco-2 - 0.8538 85.38%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4826 48.26%
OATP2B1 inhibitior - 0.7142 71.42%
OATP1B1 inhibitior + 0.8343 83.43%
OATP1B3 inhibitior + 0.9294 92.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9544 95.44%
BSEP inhibitior + 0.9854 98.54%
P-glycoprotein inhibitior + 0.8156 81.56%
P-glycoprotein substrate + 0.7859 78.59%
CYP3A4 substrate + 0.7254 72.54%
CYP2C9 substrate + 0.5985 59.85%
CYP2D6 substrate - 0.8841 88.41%
CYP3A4 inhibition - 0.7977 79.77%
CYP2C9 inhibition - 0.6218 62.18%
CYP2C19 inhibition - 0.6195 61.95%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.7401 74.01%
CYP2C8 inhibition + 0.7189 71.89%
CYP inhibitory promiscuity - 0.5932 59.32%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4845 48.45%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9031 90.31%
Skin irritation - 0.8186 81.86%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7118 71.18%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8970 89.70%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7233 72.33%
Acute Oral Toxicity (c) III 0.5223 52.23%
Estrogen receptor binding + 0.7899 78.99%
Androgen receptor binding + 0.7510 75.10%
Thyroid receptor binding + 0.6590 65.90%
Glucocorticoid receptor binding + 0.7608 76.08%
Aromatase binding + 0.6445 64.45%
PPAR gamma + 0.7742 77.42%
Honey bee toxicity - 0.7191 71.91%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.8743 87.43%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.00% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.62% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.16% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 98.11% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.26% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 97.25% 91.49%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 94.81% 81.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 94.34% 93.10%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.85% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.81% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 92.18% 94.42%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.00% 82.69%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 90.40% 96.00%
CHEMBL4208 P20618 Proteasome component C5 89.26% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.85% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.73% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.36% 93.00%
CHEMBL3891 P07384 Calpain 1 86.22% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.13% 95.89%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.39% 95.17%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.63% 96.90%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.66% 89.34%
CHEMBL2996 Q05655 Protein kinase C delta 81.82% 97.79%
CHEMBL5028 O14672 ADAM10 81.62% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.60% 95.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.21% 96.67%

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.
Semialarium mexicanum

Cross-Links

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PubChem 162855350
LOTUS LTS0263677
wikiData Q105337887