methyl 2-[(1S,2S,4R,5R,10S,12S,14R)-2,5-diacetyloxy-7,12-dimethyl-17-oxo-11,16,18,19-tetraoxapentacyclo[12.2.2.16,9.01,15.010,12]nonadeca-6,8-dien-4-yl]prop-2-enoate

Details

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Internal ID ef8d3582-90c7-46bf-8c8a-11bb06be77d5
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name methyl 2-[(1S,2S,4R,5R,10S,12S,14R)-2,5-diacetyloxy-7,12-dimethyl-17-oxo-11,16,18,19-tetraoxapentacyclo[12.2.2.16,9.01,15.010,12]nonadeca-6,8-dien-4-yl]prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28O11/c1-10-7-15-20-24(5,35-20)9-16-21-25(36-21,23(29)34-16)17(31-12(3)26)8-14(11(2)22(28)30-6)19(18(10)33-15)32-13(4)27/h7,14,16-17,19-21H,2,8-9H2,1,3-6H3/t14-,16-,17+,19-,20-,21?,24+,25+/m1/s1
InChI Key SETTUTVEWZFWRZ-JELJFLFASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O11
Molecular Weight 504.50 g/mol
Exact Mass 504.16316171 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 11
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 2-[(1S,2S,4R,5R,10S,12S,14R)-2,5-diacetyloxy-7,12-dimethyl-17-oxo-11,16,18,19-tetraoxapentacyclo[12.2.2.16,9.01,15.010,12]nonadeca-6,8-dien-4-yl]prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 - 0.6776 67.76%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6046 60.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8626 86.26%
OATP1B3 inhibitior + 0.9259 92.59%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9040 90.40%
P-glycoprotein inhibitior + 0.8208 82.08%
P-glycoprotein substrate + 0.6222 62.22%
CYP3A4 substrate + 0.7067 70.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition + 0.7116 71.16%
CYP2C9 inhibition - 0.8767 87.67%
CYP2C19 inhibition - 0.6712 67.12%
CYP2D6 inhibition - 0.9282 92.82%
CYP1A2 inhibition - 0.6517 65.17%
CYP2C8 inhibition + 0.5890 58.90%
CYP inhibitory promiscuity - 0.6851 68.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4720 47.20%
Eye corrosion - 0.9786 97.86%
Eye irritation - 0.8813 88.13%
Skin irritation - 0.7423 74.23%
Skin corrosion - 0.9236 92.36%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5414 54.14%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.6460 64.60%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6157 61.57%
Acute Oral Toxicity (c) III 0.3861 38.61%
Estrogen receptor binding + 0.8640 86.40%
Androgen receptor binding + 0.7292 72.92%
Thyroid receptor binding + 0.6167 61.67%
Glucocorticoid receptor binding + 0.8054 80.54%
Aromatase binding + 0.5931 59.31%
PPAR gamma + 0.7767 77.67%
Honey bee toxicity - 0.6208 62.08%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9688 96.88%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.78% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.02% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.90% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.77% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.47% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.48% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 88.08% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.00% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.72% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.92% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.04% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.70% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.35% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 84.22% 94.73%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.38% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.22% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.70% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.70% 94.80%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.56% 93.04%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.69% 91.07%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163187182
LOTUS LTS0205508
wikiData Q105251493