HexA(?1-3)Hex(?1-3)Hex

Details

Top
Internal ID befa657f-6dc6-4515-83ec-df4b76b72cfd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name 6-[3,5-dihydroxy-2-(hydroxymethyl)-6-[2,3,5-trihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H30O17/c19-1-3-5(21)12(10(26)16(30)31-3)33-18-11(27)13(6(22)4(2-20)32-18)34-17-9(25)7(23)8(24)14(35-17)15(28)29/h3-14,16-27,30H,1-2H2,(H,28,29)
InChI Key WSTUGTMIAHVIJD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H30O17
Molecular Weight 518.40 g/mol
Exact Mass 518.14829948 g/mol
Topological Polar Surface Area (TPSA) 286.00 Ų
XlogP -5.50
Atomic LogP (AlogP) -7.48
H-Bond Acceptor 16
H-Bond Donor 11
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of HexA(?1-3)Hex(?1-3)Hex

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9451 94.51%
Caco-2 - 0.9218 92.18%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7647 76.47%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9180 91.80%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9349 93.49%
P-glycoprotein inhibitior - 0.7971 79.71%
P-glycoprotein substrate - 0.9818 98.18%
CYP3A4 substrate - 0.5252 52.52%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8798 87.98%
CYP3A4 inhibition - 0.9569 95.69%
CYP2C9 inhibition - 0.9464 94.64%
CYP2C19 inhibition - 0.9418 94.18%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.9680 96.80%
CYP2C8 inhibition - 0.8153 81.53%
CYP inhibitory promiscuity - 0.9098 90.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7125 71.25%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9263 92.63%
Skin irritation - 0.8918 89.18%
Skin corrosion - 0.9694 96.94%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4542 45.42%
Micronuclear - 0.7541 75.41%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9416 94.16%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6468 64.68%
Acute Oral Toxicity (c) IV 0.5991 59.91%
Estrogen receptor binding + 0.5823 58.23%
Androgen receptor binding + 0.5225 52.25%
Thyroid receptor binding - 0.5068 50.68%
Glucocorticoid receptor binding - 0.6443 64.43%
Aromatase binding + 0.6756 67.56%
PPAR gamma + 0.5810 58.10%
Honey bee toxicity - 0.7414 74.14%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6955 69.55%
Fish aquatic toxicity - 0.8332 83.32%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.46% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.78% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.52% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.75% 86.92%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.02% 94.33%
CHEMBL5255 O00206 Toll-like receptor 4 80.59% 92.50%

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.
Aegle marmelos

Cross-Links

Top
PubChem 162988862
LOTUS LTS0264736
wikiData Q105312103