[(1R,3R)-3-[(1R,4R,8R,10R,12S)-10,12-dimethyl-3-oxo-2,9-dioxatricyclo[6.3.1.04,12]dodecan-10-yl]-1-(furan-3-yl)-4-hydroxybutyl] acetate

Details

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Internal ID b9073f51-740d-4b7f-825c-df7b24dc5884
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name [(1R,3R)-3-[(1R,4R,8R,10R,12S)-10,12-dimethyl-3-oxo-2,9-dioxatricyclo[6.3.1.04,12]dodecan-10-yl]-1-(furan-3-yl)-4-hydroxybutyl] acetate
SMILES (Canonical) CC(=O)OC(CC(CO)C1(CC2C3(C(CCCC3O1)C(=O)O2)C)C)C4=COC=C4
SMILES (Isomeric) CC(=O)O[C@H](C[C@H](CO)[C@]1(C[C@@H]2[C@]3([C@@H](CCC[C@H]3O1)C(=O)O2)C)C)C4=COC=C4
InChI InChI=1S/C22H30O7/c1-13(24)27-17(14-7-8-26-12-14)9-15(11-23)21(2)10-19-22(3)16(20(25)28-19)5-4-6-18(22)29-21/h7-8,12,15-19,23H,4-6,9-11H2,1-3H3/t15-,16+,17-,18-,19-,21-,22+/m1/s1
InChI Key MXLYWBPYDLGJSF-HRSOUWATSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O7
Molecular Weight 406.50 g/mol
Exact Mass 406.19915329 g/mol
Topological Polar Surface Area (TPSA) 95.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,3R)-3-[(1R,4R,8R,10R,12S)-10,12-dimethyl-3-oxo-2,9-dioxatricyclo[6.3.1.04,12]dodecan-10-yl]-1-(furan-3-yl)-4-hydroxybutyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9575 95.75%
Caco-2 - 0.6871 68.71%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8229 82.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7479 74.79%
OATP1B3 inhibitior + 0.8041 80.41%
MATE1 inhibitior - 0.8612 86.12%
OCT2 inhibitior - 0.5364 53.64%
BSEP inhibitior + 0.8806 88.06%
P-glycoprotein inhibitior - 0.5312 53.12%
P-glycoprotein substrate + 0.5644 56.44%
CYP3A4 substrate + 0.6715 67.15%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8401 84.01%
CYP3A4 inhibition - 0.6836 68.36%
CYP2C9 inhibition - 0.6932 69.32%
CYP2C19 inhibition - 0.7854 78.54%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition - 0.8369 83.69%
CYP2C8 inhibition - 0.5782 57.82%
CYP inhibitory promiscuity - 0.8878 88.78%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6509 65.09%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9737 97.37%
Skin irritation - 0.7586 75.86%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8101 81.01%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5389 53.89%
skin sensitisation - 0.9400 94.00%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5947 59.47%
Acute Oral Toxicity (c) III 0.3754 37.54%
Estrogen receptor binding + 0.9108 91.08%
Androgen receptor binding + 0.6244 62.44%
Thyroid receptor binding + 0.6963 69.63%
Glucocorticoid receptor binding + 0.8397 83.97%
Aromatase binding + 0.7189 71.89%
PPAR gamma + 0.6069 60.69%
Honey bee toxicity - 0.7708 77.08%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9627 96.27%

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 97.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.16% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.67% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.61% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.82% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.64% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.73% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.79% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.26% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 86.03% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.99% 93.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.32% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.24% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.24% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.95% 94.80%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.22% 93.04%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.81% 99.17%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.80% 95.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.64% 97.14%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.42% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.10% 100.00%

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.
Syzygiella autumnalis

Cross-Links

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PubChem 162842475
LOTUS LTS0042494
wikiData Q105174321