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

Details

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Internal ID 9282a28c-c49d-41bb-ac94-4b59d3a7a3f4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name N-[4-[4-[4,5-dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-2,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H45NO18/c1-6-12(30)16(34)18(36)24(39-6)45-22-17(35)13(31)7(2)41-26(22)44-21-14(32)8(3)40-25(19(21)37)43-20-11(27-9(4)29)23(38)42-10(5-28)15(20)33/h6-8,10-26,28,30-38H,5H2,1-4H3,(H,27,29)
InChI Key UTJMWWBYJZRONA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H45NO18
Molecular Weight 659.60 g/mol
Exact Mass 659.26366359 g/mol
Topological Polar Surface Area (TPSA) 296.00 Ų
XlogP -5.90
Atomic LogP (AlogP) -6.52
H-Bond Acceptor 18
H-Bond Donor 11
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9793 97.93%
Caco-2 - 0.8750 87.50%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.6369 63.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7045 70.45%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8430 84.30%
P-glycoprotein inhibitior - 0.5242 52.42%
P-glycoprotein substrate - 0.7643 76.43%
CYP3A4 substrate + 0.5959 59.59%
CYP2C9 substrate - 0.8121 81.21%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition - 0.9308 93.08%
CYP2C9 inhibition - 0.9266 92.66%
CYP2C19 inhibition - 0.9313 93.13%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.9479 94.79%
CYP2C8 inhibition - 0.8164 81.64%
CYP inhibitory promiscuity - 0.7967 79.67%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6860 68.60%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9333 93.33%
Skin irritation - 0.8468 84.68%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3717 37.17%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.7396 73.96%
skin sensitisation - 0.8905 89.05%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.6160 61.60%
Acute Oral Toxicity (c) III 0.5787 57.87%
Estrogen receptor binding + 0.6121 61.21%
Androgen receptor binding - 0.5992 59.92%
Thyroid receptor binding - 0.5419 54.19%
Glucocorticoid receptor binding - 0.4703 47.03%
Aromatase binding + 0.5467 54.67%
PPAR gamma + 0.5233 52.33%
Honey bee toxicity - 0.7257 72.57%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.8955 89.55%

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 94.94% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.98% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.82% 97.36%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.40% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 87.52% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.82% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.64% 94.33%
CHEMBL2581 P07339 Cathepsin D 85.53% 98.95%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.74% 91.24%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.34% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.24% 96.61%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.64% 87.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.23% 96.00%

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 75107039
LOTUS LTS0108227
wikiData Q105278842