[4-[[3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-6,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate

Details

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Internal ID 569d02ad-7c88-4304-a09d-9071af6df258
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name [4-[[3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-6,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate
SMILES (Canonical) CC(C)CC(=O)OC1C2C(CC(C2(C)O)O)C(=CO1)COC3C(C(C(C(O3)CO)O)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC(C)CC(=O)OC1C2C(CC(C2(C)O)O)C(=CO1)COC3C(C(C(C(O3)CO)O)OC(=O)C)OC(=O)C
InChI InChI=1S/C25H38O13/c1-11(2)6-18(30)38-23-19-15(7-17(29)25(19,5)32)14(9-33-23)10-34-24-22(36-13(4)28)21(35-12(3)27)20(31)16(8-26)37-24/h9,11,15-17,19-24,26,29,31-32H,6-8,10H2,1-5H3
InChI Key NSLPUSGFOYUFTE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O13
Molecular Weight 546.60 g/mol
Exact Mass 546.23124126 g/mol
Topological Polar Surface Area (TPSA) 188.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -0.48
H-Bond Acceptor 13
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [4-[[3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-6,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7570 75.70%
Caco-2 - 0.8144 81.44%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.7486 74.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8154 81.54%
OATP1B3 inhibitior + 0.9069 90.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4894 48.94%
P-glycoprotein inhibitior + 0.6214 62.14%
P-glycoprotein substrate - 0.5626 56.26%
CYP3A4 substrate + 0.6785 67.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8787 87.87%
CYP3A4 inhibition - 0.8618 86.18%
CYP2C9 inhibition - 0.8673 86.73%
CYP2C19 inhibition - 0.9092 90.92%
CYP2D6 inhibition - 0.9413 94.13%
CYP1A2 inhibition - 0.9080 90.80%
CYP2C8 inhibition - 0.5976 59.76%
CYP inhibitory promiscuity - 0.9308 93.08%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6169 61.69%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9334 93.34%
Skin irritation - 0.6330 63.30%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5319 53.19%
skin sensitisation - 0.8711 87.11%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.4564 45.64%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.6714 67.14%
Androgen receptor binding + 0.6727 67.27%
Thyroid receptor binding - 0.6028 60.28%
Glucocorticoid receptor binding + 0.5768 57.68%
Aromatase binding - 0.5234 52.34%
PPAR gamma + 0.6049 60.49%
Honey bee toxicity - 0.7404 74.04%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9489 94.89%

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 98.48% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 97.63% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.47% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.11% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.80% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.56% 97.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.80% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.44% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 89.39% 97.79%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.31% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 85.81% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.24% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.44% 85.14%
CHEMBL5255 O00206 Toll-like receptor 4 84.27% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.67% 100.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.42% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.32% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.56% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.37% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 80.89% 94.73%

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.
Viburnum ayavacense

Cross-Links

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PubChem 85219501
LOTUS LTS0069510
wikiData Q105185116