Hex(?1-4)Hex(?1-4)6-deoxy-Hex(?1-4)6-deoxy-Hex

Details

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Internal ID 804cd886-d113-4ed5-943d-9f7a2be7cf3c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name 5-[5-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-6-methyloxane-2,3,4-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H42O19/c1-5-18(11(29)14(32)21(36)37-5)41-22-16(34)12(30)19(6(2)38-22)42-24-17(35)13(31)20(8(4-26)40-24)43-23-15(33)10(28)9(27)7(3-25)39-23/h5-36H,3-4H2,1-2H3
InChI Key YJEQJHRHYMPDHN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H42O19
Molecular Weight 634.60 g/mol
Exact Mass 634.23202911 g/mol
Topological Polar Surface Area (TPSA) 307.00 Ų
XlogP -6.90
Atomic LogP (AlogP) -7.69
H-Bond Acceptor 19
H-Bond Donor 12
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hex(?1-4)Hex(?1-4)6-deoxy-Hex(?1-4)6-deoxy-Hex

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9613 96.13%
Caco-2 - 0.8882 88.82%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.7522 75.22%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8963 89.63%
OATP1B3 inhibitior + 0.9587 95.87%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9281 92.81%
P-glycoprotein inhibitior - 0.5752 57.52%
P-glycoprotein substrate - 0.9430 94.30%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8500 85.00%
CYP3A4 inhibition - 0.9566 95.66%
CYP2C9 inhibition - 0.9476 94.76%
CYP2C19 inhibition - 0.9392 93.92%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition - 0.9592 95.92%
CYP2C8 inhibition - 0.9027 90.27%
CYP inhibitory promiscuity - 0.8786 87.86%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6902 69.02%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9255 92.55%
Skin irritation - 0.9042 90.42%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7594 75.94%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.9478 94.78%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7734 77.34%
Acute Oral Toxicity (c) III 0.4818 48.18%
Estrogen receptor binding + 0.6084 60.84%
Androgen receptor binding + 0.5519 55.19%
Thyroid receptor binding + 0.5477 54.77%
Glucocorticoid receptor binding - 0.5913 59.13%
Aromatase binding + 0.6730 67.30%
PPAR gamma + 0.5376 53.76%
Honey bee toxicity - 0.6724 67.24%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.8499 84.99%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.94% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 90.12% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.63% 86.92%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.58% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 81.98% 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.
Balanites aegyptiaca

Cross-Links

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PubChem 163011486
LOTUS LTS0146015
wikiData Q105349213