UCSF

ZINC15553094

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
July 27th, 2008 39 No

Popular Name: Uridine diphosphate-N-acetylglucosamine Uridine diphosphate-N-acetylgluc…

Find On: PubMed — Wikipedia — Google

CAS Numbers: 528-04-1 , [91183-98-1]

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

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) -5.18 -12.9 -152.9 7 20 -2 312 605.339 10 ↓

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

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, L
Formation of the active cofactor, UDP-glucuronate
HS-GAG biosynthesis
Keratan sulfate biosynthesis
Mycothiol biosynthesis
N-Glycan antennae elongation
N-glycan trimming and elongation in the cis-Golgi
O-linked glycosylation of mucins
Pre-NOTCH Processing in Golgi
Reactions specific to the complex N-glycan synthesis pathway
Reactions specific to the hybrid N-glycan synthesis pathway
Sialic acid metabolism
Synthesis of glycosylphosphatidylinositol (GPI)
Synthesis of UDP-N-acetyl-glucosamine
Transport of nucleotide sugars

Analogs ( Draw Identity 99% 90% 80% 70% )