Substance Information
In ZINC since |
Heavy atoms |
Benign functionality |
January 16th, 2014 |
0 |
No
|
Other Names:
528-04-1; C00043; UDP-N-acetyl-D-glucosamine; UDP-N-acetyl-alpha-D-glucosamine; UDP-N-acetylglucosamine
528-04-1; N-[2-[[[5-[(2,4-dioxo-1H-pyrimidin-1-yl)]-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphinoyl]oxy-hydroxy-phosphinoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide; UDP-2-acetamido-2-deoxy-alpha-D-glucose; UDP-GlcN
CHEBI:46243; CHEBI:22115; CHEBI:46287; CHEBI:13456; CHEBI:13473; CHEBI:13475; CHEBI:13476; CHEBI:9823
N-[2-[[[5-[(2,4-Dioxo-1H-pyrimidin-1-yl)]-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphinoyl]oxy-hydroxy-phosphinoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide; UDP-Acetyl-D-glucosamine; UDP-Acetyl-delta-glucosamine; UDP
N-[2-[[[5-[(2,4-Dioxo-1H-pyrimidin-1-yl)]-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphinoyl]oxy-hydroxy-phosphinoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide;UDP-a-D-N-Acetylglucosamine;UDP-Acetyl-D-glucosamine;UDP-Ace
N-[2-[[[5-[(2,4-Dioxo-1H-pyrimidin-1-yl)]-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphinoyl]oxy-hydroxy-phosphinoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide;UDP-Acetyl-D-glucosamine;UDP-Acetyl-delta-glucosamine;UDP-Ac
UDP-GlcNAc
UDP-N-acetyl-alpha-D-glucosamine
UDP-N-acetyl-alpha-D-glucosamine(2-)
UDP-N-acetyl-alpha-D-glucosamine; UDP-N-acetyl-alpha-D-glucosamine dianion
UDP-N-acetyl-D-glucosamine disodium salt
[(2R,3S,4R,5R)-5-(2,4-dioxo-3H-pyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy({[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy(hydroxy)phosphoryl}oxy)phosphinic acid
[[3-acetylamino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-hydroxy-phosphoryl]oxy-[[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy]phosphinate; [[3-acetylamino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-hydroxy-phosphoryl]oxy-[[5-(2,4-d
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SMILES
Flexibase
Annotations
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- UDP-N-ACETYL-D-GLUCOSAMINE
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Vendors
Physical Representations
Type
pH range
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xlogP
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Des A‑Pol
Apolar desolvation
(kcal/mol)
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Des Pol
Polar desolvation
(kcal/mol)
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H Don
H-bond donors
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H Acc
H-bond acceptors
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Chg
Net charge
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tPSA
(Ų)
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MWT
Molecular weight
(g/mol)
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RB
Rotatable bonds
|
DL |
Ref
Reference (pH 7)
|
-5.18 |
-12.79 |
-151.83 |
7 |
20 |
-2 |
312 |
605.339 |
10 |
↓
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Vendor Notes
Note Type |
Comments |
Provided By |
UniProt Database Links |
ALG13_ASHGO; ALG13_ASPFU; ALG13_CANAL; ALG13_CANGA; ALG13_CRYNB; ALG13_CRYNJ; ALG13_DEBHA; ALG13_HUMAN; ALG13_KLULA; ALG13_MOUSE; ALG13_RAT; ALG13_SCHPO; ALG13_YARLI; ALG13_YEAST; ALG14_ASHGO; ALG14_ASPFU; ALG14_CANAL; ALG14_CANGA; ALG14_CRYNB; ALG14_CRYN |
ChEBI |
UniProt Database Links |
EPSC_RALSL; EPSC_RALSO; GCNT1_BOVIN; GCNT1_HUMAN; GCNT1_MOUSE; GCNT2_MOUSE; GCNT3_BHV4; GCNT3_BHV4D; GCNT3_BHV4L; GCNT3_BHV4V; GCNT3_BOSMU; GCNT3_BOVIN; GCNT3_BUBBU; GCNT3_HUMAN; GCNT3_MOUSE; GCNT3_RAT; GCNT3_SHEEP; GCNT3_SYNCA; GCNT3_XENLA; GCNT4_DANRE |
ChEBI |
Reactome Database Links |
REACT_115554; REACT_115905; REACT_116000; REACT_118594; REACT_121050; REACT_121143; REACT_121277; REACT_1240; REACT_22147; REACT_22160; REACT_22287; REACT_22323; REACT_22332; REACT_22397; REACT_25005; REACT_25009; REACT_25236; REACT_25253; REACT_25314; RE |
ChEBI |
Direct Reactome Annotations (via ChEBI)
Description |
Species |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, L |
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Formation of the active cofactor, UDP-glucuronate |
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HS-GAG biosynthesis |
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Keratan sulfate biosynthesis |
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Mycothiol biosynthesis |
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N-Glycan antennae elongation |
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N-glycan trimming and elongation in the cis-Golgi |
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O-linked glycosylation of mucins |
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Pre-NOTCH Processing in Golgi |
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Reactions specific to the complex N-glycan synthesis pathway |
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Reactions specific to the hybrid N-glycan synthesis pathway |
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Sialic acid metabolism |
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Synthesis of glycosylphosphatidylinositol (GPI) |
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Synthesis of UDP-N-acetyl-glucosamine |
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Transport of nucleotide sugars |
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No pre-computed analogs available. Try a structural similarity search.