Fischeroside A

Details

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Internal ID 05542d70-d6d3-4dec-a731-44d04cb1b0e5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name [(1R,2S,6R,10S,11R,13S,15R)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-8-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40O11/c1-12-6-18-26(35,23(12)34)9-15(11-37-24-21(33)20(32)19(31)17(10-29)38-24)7-16-22-25(4,5)27(22,39-14(3)30)8-13(2)28(16,18)36/h6-7,13,16-22,24,29,31-33,35-36H,8-11H2,1-5H3/t13-,16+,17-,18-,19-,20+,21-,22-,24-,26-,27+,28-/m1/s1
InChI Key JMDGBSYRPFFZBO-WHDWRCRCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O11
Molecular Weight 552.60 g/mol
Exact Mass 552.25706209 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.65
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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RefChem:921619
((1R,2S,6R,10S,11R,13S,15R)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-8-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxymethyl)-13-tetracyclo(8.5.0.02,6.011,13)pentadeca-3,8-dienyl) acetate
CHEBI:69815
Fischerosides A
CHEMBL1813581
Q27138157
(1aR,1bS,4aR,7aS,7bR,8R,9aS)-3-[(beta-D-Glucopyranosyloxy)methyl]-4a,7b-dihydroxy-1,1,6,8-tetramethyl-5-oxo-1,1a,1b,4,4a,5,7a,7b,8,9-decahydro-9aH-cyclopropa[3,4]benzo[1,2-e]azulen-9a-yl acetate
[dihydroxy-tetramethyl-oxo-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl][?]yl] acetate

2D Structure

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2D Structure of Fischeroside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8070 80.70%
Caco-2 - 0.8454 84.54%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6511 65.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8527 85.27%
OATP1B3 inhibitior + 0.9251 92.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6070 60.70%
P-glycoprotein inhibitior - 0.4566 45.66%
P-glycoprotein substrate - 0.5863 58.63%
CYP3A4 substrate + 0.6993 69.93%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.9014 90.14%
CYP3A4 inhibition - 0.8464 84.64%
CYP2C9 inhibition - 0.7193 71.93%
CYP2C19 inhibition - 0.8423 84.23%
CYP2D6 inhibition - 0.9216 92.16%
CYP1A2 inhibition - 0.8177 81.77%
CYP2C8 inhibition + 0.5230 52.30%
CYP inhibitory promiscuity - 0.8714 87.14%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6878 68.78%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9290 92.90%
Skin irritation - 0.6863 68.63%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4509 45.09%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.7429 74.29%
skin sensitisation - 0.8351 83.51%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6832 68.32%
Acute Oral Toxicity (c) III 0.5341 53.41%
Estrogen receptor binding + 0.7160 71.60%
Androgen receptor binding + 0.7100 71.00%
Thyroid receptor binding - 0.5174 51.74%
Glucocorticoid receptor binding + 0.6899 68.99%
Aromatase binding + 0.7503 75.03%
PPAR gamma + 0.6221 62.21%
Honey bee toxicity - 0.7317 73.17%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9159 91.59%

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 97.68% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.65% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.42% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.74% 98.95%
CHEMBL4794 Q8NER1 Vanilloid receptor 89.27% 98.97%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.20% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.64% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.97% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.70% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.35% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.68% 100.00%
CHEMBL4208 P20618 Proteasome component C5 83.89% 90.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.83% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.28% 99.23%
CHEMBL5255 O00206 Toll-like receptor 4 82.15% 92.50%
CHEMBL3401 O75469 Pregnane X receptor 81.96% 94.73%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.72% 96.61%

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.
Euphorbia fischeriana

Cross-Links

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PubChem 53360347
NPASS NPC222307
ChEMBL CHEMBL1813581
LOTUS LTS0063528
wikiData Q27138157