Hex(?1-3)Hex(?1-4)Hex(?1-4)Hex(?1-6)Hex

Details

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Internal ID e6e8b30a-b6b1-4240-8c7e-2c547ee59d71
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name 6-[[5-[5-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxane-2,3,4,5-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H52O26/c31-1-6-11(35)15(39)19(43)28(50-6)56-25-13(37)7(2-32)51-30(22(25)46)55-24-9(4-34)53-29(21(45)17(24)41)54-23-8(3-33)52-27(20(44)16(23)40)48-5-10-12(36)14(38)18(42)26(47)49-10/h6-47H,1-5H2
InChI Key MHFQYDDXXOOWNG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H52O26
Molecular Weight 828.70 g/mol
Exact Mass 828.27468176 g/mol
Topological Polar Surface Area (TPSA) 427.00 Ų
XlogP -10.60
Atomic LogP (AlogP) -11.92
H-Bond Acceptor 26
H-Bond Donor 17
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hex(?1-3)Hex(?1-4)Hex(?1-4)Hex(?1-6)Hex

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9680 96.80%
Caco-2 - 0.8809 88.09%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.7116 71.16%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9559 95.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5087 50.87%
P-glycoprotein inhibitior + 0.6073 60.73%
P-glycoprotein substrate - 0.9427 94.27%
CYP3A4 substrate + 0.5182 51.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8414 84.14%
CYP3A4 inhibition - 0.9645 96.45%
CYP2C9 inhibition - 0.9376 93.76%
CYP2C19 inhibition - 0.9083 90.83%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.9610 96.10%
CYP2C8 inhibition - 0.8197 81.97%
CYP inhibitory promiscuity - 0.8898 88.98%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6495 64.95%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.8941 89.41%
Skin irritation - 0.8992 89.92%
Skin corrosion - 0.9738 97.38%
Ames mutagenesis - 0.8554 85.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8405 84.05%
Micronuclear - 0.7941 79.41%
Hepatotoxicity - 0.9500 95.00%
skin sensitisation - 0.9455 94.55%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7145 71.45%
Acute Oral Toxicity (c) IV 0.6266 62.66%
Estrogen receptor binding + 0.7195 71.95%
Androgen receptor binding + 0.5651 56.51%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.7086 70.86%
Aromatase binding + 0.6213 62.13%
PPAR gamma + 0.6381 63.81%
Honey bee toxicity - 0.6193 61.93%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.8800 88.00%

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 93.84% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 93.37% 95.93%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.33% 83.57%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.83% 86.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.49% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.34% 96.61%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162947974
LOTUS LTS0004628
wikiData Q105163792