[(2R,4R,6R,10S,12R,13R)-13-acetyloxy-4,15-dimethyl-12-(2-methyloxiran-2-yl)-8-oxo-3,7,17-trioxatetracyclo[12.2.1.16,9.02,4]octadeca-1(16),9(18),14-trien-10-yl] acetate

Details

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Internal ID da1db21c-cda7-421f-b7e5-4aaef7b69934
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name [(2R,4R,6R,10S,12R,13R)-13-acetyloxy-4,15-dimethyl-12-(2-methyloxiran-2-yl)-8-oxo-3,7,17-trioxatetracyclo[12.2.1.16,9.02,4]octadeca-1(16),9(18),14-trien-10-yl] acetate
SMILES (Canonical) CC1=C2C(C(CC(C3=CC(CC4(C(O4)C(=C1)O2)C)OC3=O)OC(=O)C)C5(CO5)C)OC(=O)C
SMILES (Isomeric) CC1=C2[C@@H]([C@@H](C[C@@H](C3=C[C@@H](C[C@@]4([C@@H](O4)C(=C1)O2)C)OC3=O)OC(=O)C)C5(CO5)C)OC(=O)C
InChI InChI=1S/C24H28O9/c1-11-6-18-21-23(4,33-21)9-14-7-15(22(27)31-14)17(29-12(2)25)8-16(24(5)10-28-24)20(19(11)32-18)30-13(3)26/h6-7,14,16-17,20-21H,8-10H2,1-5H3/t14-,16+,17-,20+,21-,23+,24?/m0/s1
InChI Key ZKPQWDXTJKFKDU-MPROZZDNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28O9
Molecular Weight 460.50 g/mol
Exact Mass 460.17333247 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,4R,6R,10S,12R,13R)-13-acetyloxy-4,15-dimethyl-12-(2-methyloxiran-2-yl)-8-oxo-3,7,17-trioxatetracyclo[12.2.1.16,9.02,4]octadeca-1(16),9(18),14-trien-10-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 + 0.9941 99.41%
Caco-2 - 0.5502 55.02%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7757 77.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8510 85.10%
OATP1B3 inhibitior + 0.8989 89.89%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9265 92.65%
P-glycoprotein inhibitior + 0.8235 82.35%
P-glycoprotein substrate + 0.5271 52.71%
CYP3A4 substrate + 0.6783 67.83%
CYP2C9 substrate - 0.8097 80.97%
CYP2D6 substrate - 0.8842 88.42%
CYP3A4 inhibition - 0.6084 60.84%
CYP2C9 inhibition - 0.7246 72.46%
CYP2C19 inhibition - 0.7727 77.27%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.6580 65.80%
CYP2C8 inhibition + 0.5703 57.03%
CYP inhibitory promiscuity - 0.7807 78.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5232 52.32%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.9089 90.89%
Skin irritation - 0.7201 72.01%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5519 55.19%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5175 51.75%
skin sensitisation - 0.7721 77.21%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6454 64.54%
Acute Oral Toxicity (c) III 0.3625 36.25%
Estrogen receptor binding + 0.7405 74.05%
Androgen receptor binding + 0.7101 71.01%
Thyroid receptor binding + 0.5183 51.83%
Glucocorticoid receptor binding + 0.8189 81.89%
Aromatase binding - 0.5458 54.58%
PPAR gamma + 0.7522 75.22%
Honey bee toxicity - 0.6855 68.55%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9968 99.68%

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 97.43% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.05% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.77% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.71% 89.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.15% 94.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.01% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.88% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.93% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.68% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.63% 96.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.16% 81.11%
CHEMBL2581 P07339 Cathepsin D 85.48% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.62% 94.73%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.79% 93.04%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.22% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.73% 97.09%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.21% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.18% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.64% 94.00%

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.
There are no matching plants.

Cross-Links

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PubChem 101607297
LOTUS LTS0251058
wikiData Q105378635