Jaslanceoside B

Details

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Internal ID 25839a39-4ba8-42ac-a19e-b3353381c08a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (4S,5Z,6S)-5-[2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30O14/c1-36-20(30)10-16-15(8-9-37-19(29)7-4-13-2-5-14(28)6-3-13)25(38-12-17(16)24(34)35)40-26-23(33)22(32)21(31)18(11-27)39-26/h2-8,12,16,18,21-23,25-28,31-33H,9-11H2,1H3,(H,34,35)/b7-4+,15-8-/t16-,18+,21+,22-,23+,25-,26-/m0/s1
InChI Key MGEVYVDQMTWJNV-HOPHSATRSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O14
Molecular Weight 566.50 g/mol
Exact Mass 566.16355563 g/mol
Topological Polar Surface Area (TPSA) 219.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.80
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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(4S,5Z,6S)-5-[2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid
188300-82-5
DTXSID701347048

2D Structure

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2D Structure of Jaslanceoside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6083 60.83%
Caco-2 - 0.9037 90.37%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Mitochondria 0.7128 71.28%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.7401 74.01%
OATP1B3 inhibitior + 0.9527 95.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8620 86.20%
P-glycoprotein inhibitior - 0.4798 47.98%
P-glycoprotein substrate - 0.5459 54.59%
CYP3A4 substrate + 0.6586 65.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8725 87.25%
CYP3A4 inhibition - 0.9630 96.30%
CYP2C9 inhibition - 0.8562 85.62%
CYP2C19 inhibition - 0.8298 82.98%
CYP2D6 inhibition - 0.9029 90.29%
CYP1A2 inhibition - 0.8749 87.49%
CYP2C8 inhibition + 0.7954 79.54%
CYP inhibitory promiscuity - 0.8558 85.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7291 72.91%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9324 93.24%
Skin irritation - 0.8203 82.03%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis - 0.5893 58.93%
Human Ether-a-go-go-Related Gene inhibition - 0.4277 42.77%
Micronuclear - 0.6326 63.26%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8534 85.34%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5789 57.89%
Acute Oral Toxicity (c) III 0.6045 60.45%
Estrogen receptor binding + 0.7804 78.04%
Androgen receptor binding + 0.6983 69.83%
Thyroid receptor binding - 0.5276 52.76%
Glucocorticoid receptor binding + 0.6122 61.22%
Aromatase binding - 0.4842 48.42%
PPAR gamma + 0.6996 69.96%
Honey bee toxicity - 0.7523 75.23%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8964 89.64%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.26% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.21% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.03% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.79% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.07% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.26% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.81% 89.00%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 85.37% 89.67%
CHEMBL3194 P02766 Transthyretin 84.70% 90.71%
CHEMBL2581 P07339 Cathepsin D 83.09% 98.95%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 82.54% 95.64%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.88% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 80.83% 91.49%

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.
Chrysojasminum floridum
Jasminum elongatum

Cross-Links

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PubChem 45359788
LOTUS LTS0008178
wikiData Q105163270