[(1R,3S,5R,7R,8R,9R,10R,15R)-15-[(3R)-2,2-dimethyl-5-oxooxolan-3-yl]-7-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-8,15-dimethyl-2-methylidene-12-oxo-4,11-dioxatetracyclo[8.5.0.03,5.03,8]pentadec-13-en-9-yl] acetate

Details

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Internal ID c40b8c3f-c18e-43dc-9034-ea1f8370ec51
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name [(1R,3S,5R,7R,8R,9R,10R,15R)-15-[(3R)-2,2-dimethyl-5-oxooxolan-3-yl]-7-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-8,15-dimethyl-2-methylidene-12-oxo-4,11-dioxatetracyclo[8.5.0.03,5.03,8]pentadec-13-en-9-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O10/c1-12-21-22(35-18(30)7-8-26(21,5)16-11-20(32)38-25(16,3)4)23(34-13(2)29)27(6)15(10-17-28(12,27)37-17)14-9-19(31)36-24(14)33/h7-9,15-17,21-24,33H,1,10-11H2,2-6H3/t15-,16-,17+,21+,22+,23-,24+,26-,27+,28+/m0/s1
InChI Key QBKSPXLEBYOGMB-HAPGUVSRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O10
Molecular Weight 528.50 g/mol
Exact Mass 528.19954721 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,3S,5R,7R,8R,9R,10R,15R)-15-[(3R)-2,2-dimethyl-5-oxooxolan-3-yl]-7-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-8,15-dimethyl-2-methylidene-12-oxo-4,11-dioxatetracyclo[8.5.0.03,5.03,8]pentadec-13-en-9-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 + 0.9685 96.85%
Caco-2 - 0.7805 78.05%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7170 71.70%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.7994 79.94%
OATP1B3 inhibitior + 0.8005 80.05%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8963 89.63%
P-glycoprotein inhibitior + 0.7965 79.65%
P-glycoprotein substrate + 0.6191 61.91%
CYP3A4 substrate + 0.7127 71.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8855 88.55%
CYP3A4 inhibition + 0.7842 78.42%
CYP2C9 inhibition - 0.8121 81.21%
CYP2C19 inhibition - 0.7592 75.92%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.8710 87.10%
CYP2C8 inhibition + 0.6461 64.61%
CYP inhibitory promiscuity - 0.7681 76.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4924 49.24%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.8958 89.58%
Skin irritation - 0.6487 64.87%
Skin corrosion - 0.8906 89.06%
Ames mutagenesis - 0.5970 59.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.7327 73.27%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5364 53.64%
Acute Oral Toxicity (c) I 0.3404 34.04%
Estrogen receptor binding + 0.7277 72.77%
Androgen receptor binding + 0.7364 73.64%
Thyroid receptor binding + 0.6234 62.34%
Glucocorticoid receptor binding + 0.8038 80.38%
Aromatase binding + 0.6713 67.13%
PPAR gamma + 0.7272 72.72%
Honey bee toxicity - 0.6713 67.13%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9799 97.99%

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 98.85% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.59% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 93.97% 91.19%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.55% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.82% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.80% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.29% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.69% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.33% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.55% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.55% 85.14%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.54% 91.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.21% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.72% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.45% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.23% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.21% 96.77%
CHEMBL2996 Q05655 Protein kinase C delta 81.00% 97.79%

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.
Munronia pinnata

Cross-Links

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PubChem 162932545
LOTUS LTS0265057
wikiData Q105217864