HexA(?1-3)Hex(?1-2)6-deoxy-Hex

Details

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Internal ID 7f12008e-5619-4b4f-b0ca-7fdfcbf3ac42
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name 6-[3,5-dihydroxy-2-(hydroxymethyl)-6-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxyoxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H30O16/c1-3-5(20)8(23)14(16(29)30-3)34-18-11(26)12(6(21)4(2-19)31-18)32-17-10(25)7(22)9(24)13(33-17)15(27)28/h3-14,16-26,29H,2H2,1H3,(H,27,28)
InChI Key ITRSBVNKBJUKEK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O16
Molecular Weight 502.40 g/mol
Exact Mass 502.15338487 g/mol
Topological Polar Surface Area (TPSA) 266.00 Ų
XlogP -5.00
Atomic LogP (AlogP) -6.45
H-Bond Acceptor 15
H-Bond Donor 10
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of HexA(?1-3)Hex(?1-2)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 - 0.8040 80.40%
Caco-2 - 0.9172 91.72%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.8119 81.19%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8947 89.47%
OATP1B3 inhibitior + 0.9276 92.76%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9140 91.40%
P-glycoprotein inhibitior - 0.8035 80.35%
P-glycoprotein substrate - 0.9362 93.62%
CYP3A4 substrate + 0.5374 53.74%
CYP2C9 substrate - 0.8076 80.76%
CYP2D6 substrate - 0.8878 88.78%
CYP3A4 inhibition - 0.9581 95.81%
CYP2C9 inhibition - 0.9653 96.53%
CYP2C19 inhibition - 0.9657 96.57%
CYP2D6 inhibition - 0.9677 96.77%
CYP1A2 inhibition - 0.9608 96.08%
CYP2C8 inhibition - 0.8014 80.14%
CYP inhibitory promiscuity - 0.9056 90.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7510 75.10%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9473 94.73%
Skin irritation - 0.8647 86.47%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.6654 66.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5648 56.48%
Micronuclear - 0.7041 70.41%
Hepatotoxicity - 0.8591 85.91%
skin sensitisation - 0.9338 93.38%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.8206 82.06%
Acute Oral Toxicity (c) III 0.5751 57.51%
Estrogen receptor binding + 0.6050 60.50%
Androgen receptor binding - 0.5893 58.93%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6237 62.37%
Aromatase binding + 0.6200 62.00%
PPAR gamma + 0.5236 52.36%
Honey bee toxicity - 0.7975 79.75%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7355 73.55%
Fish aquatic toxicity - 0.8158 81.58%

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
CHEMBL1951 P21397 Monoamine oxidase A 90.37% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.61% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.61% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.71% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 82.70% 92.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.75% 94.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.85% 86.92%

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.
Aegle marmelos

Cross-Links

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PubChem 162913076
LOTUS LTS0234563
wikiData Q105120254