[(1S,2S,5S,6S,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-21-yl] acetate

Details

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Internal ID 07d32d2c-1dfe-496d-bf33-827825973196
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(1S,2S,5S,6S,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-21-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H36O9/c1-13(29)36-20-9-19(32)27-12-35-23(33)25(20,3)17(27)8-18(31)26(4)22(27)16(30)10-24(2)15(14-5-6-34-11-14)7-21-28(24,26)37-21/h5-6,11,15,17-23,31-33H,7-10,12H2,1-4H3/t15-,17-,18+,19-,20+,21+,22+,23+,24-,25+,26+,27+,28+/m0/s1
InChI Key DTKVYFQSFHHKAR-PPQCXHAGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H36O9
Molecular Weight 516.60 g/mol
Exact Mass 516.23593272 g/mol
Topological Polar Surface Area (TPSA) 139.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,5S,6S,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-21-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 + 0.9723 97.23%
Caco-2 - 0.7405 74.05%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7978 79.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3683 36.83%
OATP1B3 inhibitior + 0.8467 84.67%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8614 86.14%
BSEP inhibitior + 0.9215 92.15%
P-glycoprotein inhibitior + 0.6183 61.83%
P-glycoprotein substrate + 0.5566 55.66%
CYP3A4 substrate + 0.7202 72.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8417 84.17%
CYP3A4 inhibition - 0.5471 54.71%
CYP2C9 inhibition - 0.8020 80.20%
CYP2C19 inhibition - 0.8689 86.89%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition - 0.8660 86.60%
CYP2C8 inhibition + 0.6435 64.35%
CYP inhibitory promiscuity - 0.9222 92.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5684 56.84%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9200 92.00%
Skin irritation - 0.7312 73.12%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7918 79.18%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8944 89.44%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.5434 54.34%
Acute Oral Toxicity (c) I 0.5851 58.51%
Estrogen receptor binding + 0.8496 84.96%
Androgen receptor binding + 0.7458 74.58%
Thyroid receptor binding + 0.5693 56.93%
Glucocorticoid receptor binding + 0.7473 74.73%
Aromatase binding + 0.7546 75.46%
PPAR gamma + 0.6472 64.72%
Honey bee toxicity - 0.7241 72.41%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9890 98.90%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.60% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.43% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.98% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.34% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.18% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.52% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.14% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 89.85% 91.19%
CHEMBL2581 P07339 Cathepsin D 87.80% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.18% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.70% 85.14%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.98% 97.28%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.12% 99.23%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.42% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.77% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.98% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.98% 82.69%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.64% 92.62%
CHEMBL5028 O14672 ADAM10 80.39% 97.50%

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.
Pterorhachis zenkeri

Cross-Links

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PubChem 162946249
LOTUS LTS0213120
wikiData Q104988851