3-(3-Acetamido-6-carbamoyl-4,5-dihydroxyoxan-2-yl)oxy-6-(2-acetamido-1,4,5-trihydroxyhexan-3-yl)oxy-5-formamido-4-hydroxyoxane-2-carboxamide

Details

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Internal ID 33ac41cd-76a1-4665-b790-563dcb31a046
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > N-acyl-alpha-hexosamines
IUPAC Name 3-(3-acetamido-6-carbamoyl-4,5-dihydroxyoxan-2-yl)oxy-6-(2-acetamido-1,4,5-trihydroxyhexan-3-yl)oxy-5-formamido-4-hydroxyoxane-2-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H39N5O15/c1-6(31)12(34)16(9(4-29)27-7(2)32)40-22-10(26-5-30)14(36)17(19(43-22)21(25)39)41-23-11(28-8(3)33)13(35)15(37)18(42-23)20(24)38/h5-6,9-19,22-23,29,31,34-37H,4H2,1-3H3,(H2,24,38)(H2,25,39)(H,26,30)(H,27,32)(H,28,33)
InChI Key RLBLYZKFNSJEQQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H39N5O15
Molecular Weight 625.60 g/mol
Exact Mass 625.24426555 g/mol
Topological Polar Surface Area (TPSA) 332.00 Ų
XlogP -7.10
Atomic LogP (AlogP) -7.88
H-Bond Acceptor 15
H-Bond Donor 11
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3-Acetamido-6-carbamoyl-4,5-dihydroxyoxan-2-yl)oxy-6-(2-acetamido-1,4,5-trihydroxyhexan-3-yl)oxy-5-formamido-4-hydroxyoxane-2-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9747 97.47%
Caco-2 - 0.8805 88.05%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.4106 41.06%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8303 83.03%
OATP1B3 inhibitior + 0.9350 93.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8727 87.27%
P-glycoprotein inhibitior - 0.4306 43.06%
P-glycoprotein substrate + 0.6240 62.40%
CYP3A4 substrate + 0.6535 65.35%
CYP2C9 substrate - 0.8133 81.33%
CYP2D6 substrate - 0.8764 87.64%
CYP3A4 inhibition - 0.7810 78.10%
CYP2C9 inhibition - 0.8920 89.20%
CYP2C19 inhibition - 0.9289 92.89%
CYP2D6 inhibition - 0.9330 93.30%
CYP1A2 inhibition - 0.9466 94.66%
CYP2C8 inhibition - 0.5590 55.90%
CYP inhibitory promiscuity - 0.8901 89.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5962 59.62%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9272 92.72%
Skin irritation - 0.8189 81.89%
Skin corrosion - 0.9490 94.90%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7507 75.07%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5997 59.97%
skin sensitisation - 0.8939 89.39%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8530 85.30%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.6550 65.50%
Acute Oral Toxicity (c) III 0.6021 60.21%
Estrogen receptor binding + 0.6490 64.90%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.4928 49.28%
Glucocorticoid receptor binding + 0.5986 59.86%
Aromatase binding - 0.4845 48.45%
PPAR gamma + 0.6281 62.81%
Honey bee toxicity - 0.7032 70.32%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.8829 88.29%

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 96.97% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.86% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.29% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.28% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.23% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 91.25% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.76% 97.25%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 87.93% 94.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.42% 94.45%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 86.38% 97.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.22% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.52% 85.14%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.40% 89.50%
CHEMBL2094135 Q96BI3 Gamma-secretase 84.81% 98.05%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.74% 95.89%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.99% 95.58%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.82% 96.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.56% 94.00%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 82.01% 95.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.95% 97.29%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.50% 96.47%
CHEMBL4015 P41597 C-C chemokine receptor type 2 81.42% 98.57%
CHEMBL3776 Q14790 Caspase-8 81.42% 97.06%
CHEMBL340 P08684 Cytochrome P450 3A4 81.09% 91.19%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 81.08% 88.00%
CHEMBL5028 O14672 ADAM10 80.73% 97.50%
CHEMBL226 P30542 Adenosine A1 receptor 80.29% 95.93%

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 162981926
LOTUS LTS0000174
wikiData Q105239751