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

Details

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Internal ID a7a3d14a-5fdf-4b0b-a3ce-115c2e77021c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name 6-[[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]oxane-2,3,4,5-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O14/c1-4-7(19)10(22)13(25)18(30-4)32-15-8(20)5(2)29-17(14(15)26)28-3-6-9(21)11(23)12(24)16(27)31-6/h4-27H,3H2,1-2H3
InChI Key BOYXSBZYWFJKTN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O14
Molecular Weight 472.40 g/mol
Exact Mass 472.17920569 g/mol
Topological Polar Surface Area (TPSA) 228.00 Ų
XlogP -5.30
Atomic LogP (AlogP) -5.52
H-Bond Acceptor 14
H-Bond Donor 9
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-deoxy-Hex(?1-3)6-deoxy-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 - 0.9326 93.26%
Caco-2 - 0.8947 89.47%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7970 79.70%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9046 90.46%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9176 91.76%
P-glycoprotein inhibitior - 0.8235 82.35%
P-glycoprotein substrate - 0.9037 90.37%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8457 84.57%
CYP3A4 inhibition - 0.9279 92.79%
CYP2C9 inhibition - 0.9373 93.73%
CYP2C19 inhibition - 0.9389 93.89%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.9545 95.45%
CYP2C8 inhibition - 0.8598 85.98%
CYP inhibitory promiscuity - 0.8475 84.75%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6893 68.93%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9554 95.54%
Skin irritation - 0.8836 88.36%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis - 0.7108 71.08%
Human Ether-a-go-go-Related Gene inhibition + 0.6908 69.08%
Micronuclear - 0.6267 62.67%
Hepatotoxicity - 0.7822 78.22%
skin sensitisation - 0.9388 93.88%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7667 76.67%
Acute Oral Toxicity (c) III 0.6264 62.64%
Estrogen receptor binding - 0.5754 57.54%
Androgen receptor binding - 0.7403 74.03%
Thyroid receptor binding + 0.6823 68.23%
Glucocorticoid receptor binding - 0.6374 63.74%
Aromatase binding + 0.6575 65.75%
PPAR gamma + 0.5511 55.11%
Honey bee toxicity - 0.7623 76.23%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.7183 71.83%

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 92.78% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.26% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 92.23% 95.93%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 90.41% 83.57%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.68% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.37% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.83% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.79% 86.92%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.58% 97.25%

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.
Rhamnus cathartica

Cross-Links

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PubChem 162994272
LOTUS LTS0203976
wikiData Q104197892