Syributin 2

Details

Top
Internal ID 15b74bf4-36c9-4d63-a61c-f349a8d3d8c6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name [(2R,3R)-2,3-dihydroxy-3-(5-oxo-2H-furan-3-yl)propyl] octanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O6/c1-2-3-4-5-6-7-13(17)21-10-12(16)15(19)11-8-14(18)20-9-11/h8,12,15-16,19H,2-7,9-10H2,1H3/t12-,15-/m1/s1
InChI Key CRYYXCIYGAGGEP-IUODEOHRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O6
Molecular Weight 300.35 g/mol
Exact Mass 300.15728848 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Syributin 2

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9155 91.55%
Caco-2 - 0.6258 62.58%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8037 80.37%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6804 68.04%
P-glycoprotein inhibitior - 0.8379 83.79%
P-glycoprotein substrate - 0.6112 61.12%
CYP3A4 substrate + 0.5246 52.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8959 89.59%
CYP3A4 inhibition - 0.7730 77.30%
CYP2C9 inhibition - 0.8349 83.49%
CYP2C19 inhibition - 0.7044 70.44%
CYP2D6 inhibition - 0.8861 88.61%
CYP1A2 inhibition - 0.6965 69.65%
CYP2C8 inhibition - 0.9111 91.11%
CYP inhibitory promiscuity - 0.9397 93.97%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6643 66.43%
Eye corrosion - 0.9846 98.46%
Eye irritation - 0.7556 75.56%
Skin irritation - 0.6210 62.10%
Skin corrosion - 0.9331 93.31%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6701 67.01%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation - 0.9342 93.42%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6617 66.17%
Acute Oral Toxicity (c) III 0.5487 54.87%
Estrogen receptor binding + 0.6168 61.68%
Androgen receptor binding - 0.7011 70.11%
Thyroid receptor binding + 0.6171 61.71%
Glucocorticoid receptor binding + 0.6138 61.38%
Aromatase binding - 0.8153 81.53%
PPAR gamma - 0.5961 59.61%
Honey bee toxicity - 0.9681 96.81%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6528 65.28%
Fish aquatic toxicity + 0.9600 96.00%

Targets

Top

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
CHEMBL230 P35354 Cyclooxygenase-2 98.51% 89.63%
CHEMBL2581 P07339 Cathepsin D 98.11% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.97% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.56% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.34% 94.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.87% 85.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.30% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 87.22% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.84% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.72% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.29% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.94% 90.71%
CHEMBL5255 O00206 Toll-like receptor 4 84.68% 92.50%
CHEMBL299 P17252 Protein kinase C alpha 84.61% 98.03%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.05% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.53% 91.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.17% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.85% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.50% 97.29%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 9994961
LOTUS LTS0004028
wikiData Q104969008