U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C8H15NO6
Molecular Weight 221.2078
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .BETA.-N-ACETYL-D-GALACTOSAMINE

SMILES

CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@H](O)[C@@H]1O

InChI

InChIKey=OVRNDRQMDRJTHS-JAJWTYFOSA-N
InChI=1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6+,7-,8-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H15NO6
Molecular Weight 221.2078
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: The description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/28418238 | https://www.ncbi.nlm.nih.gov/pubmed/26788060 | https://www.ncbi.nlm.nih.gov/pubmed/26854615 | https://www.ncbi.nlm.nih.gov/pubmed/24603437

β-N-Acetyl-D-galactosamine (GalNAc) is an amino sugar derived from galactose found in O-linked and N-linked glycans. As an essential sugar, the role is basically the same for N-acetylgalactosamine as it is for the others, which is to enhance cellular communication. Although there has not been much research to date, what has been done reveals that this saccharide may inhibit the growth of some tumors. For example, colon cancer patients have only half the normal amounts of N-acetylgalactosamine. Studies have shown that colon cancer cells that metastasize make more mucin, making them more likely to form metastases. Therefore, it appears that N-acetylgalactosamine plays an important role in preventing this formation from occurring. N-acetylgalactosamine and N-acetylglucosamine glycans is a predictor of metastasis and poor prognosis in a number of human adenocarcinomas, including breast cancer. Lower than normal levels of this sugar has been found in patients with heart disease implying that these conditions may be reversed if a supplementation of N-acetylgalactosamine were to be added to the diet. It appears that β-N-Acetyl-D-galactosamine plays a role in joint function, sweeping away destructive free radicals that can cause inflammation. N-acetylgalactosamine also seems to play an important role in the immune system. Contained in macrophages and neutrophils, it may play a significant role in the etiology of joint inflammation and could be important in such conditions as rheumatoid arthritis. In humans, it is the terminal carbohydrate forming the antigen of blood group A. N-acetylgalactosamine (GalNAc) is a well-defined liver-targeted moiety benefiting from its high affinity with asialoglycoprotein receptor (ASGPR). By conjugating it directly to the oligonucleotides or decorating it to a certain delivery system as a targeting moiety, GalNAc has achieved compelling successes in the development of nucleic acid therapeutics in recent years. Several oligonucleotide modalities are undergoing pivotal clinical studies, followed by a blooming pipeline in the preclinical stage. N-Acetyl-D-galactosamine is used in affinity chromatography, protein chromatography and in carbohydrate matrices. N-Acetyl-D-galactosamine has been used to study periodontal disease and to facilitate the design of potent small-molecule ice recrystallization inhibitors. N-Acetyl-D-galactosamine has also been used to demonstrate a molecular shuttle between extracellular and cytoplasmic space allows for monitoring of GAG biosynthesis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Capillary electrophoresis for rapid profiling of organic acidurias.
1998 Sep
Unbalanced effects of dermatan sulfates with different sulfation patterns on coagulation, thrombosis and bleeding.
2001 Nov
Structure and anticoagulant properties of sulfated glycosaminoglycans from primitive Chordates.
2002 Mar
Evaluation of filter paper collection of urine samples for detection and measurement of organic acidurias by capillary electrophoresis.
2002 Nov 15
Chemical diagnosis of Lesch-Nyhan syndrome using gas chromatography-mass spectrometry detection.
2003 Jul 15
Conformational behavior of chondroitin and chondroitin sulfate in relation to their physical properties as inferred by molecular modeling.
2003 May
Venous and arterial thrombosis in rat models: dissociation of the antithrombotic effects of glycosaminoglycans.
2004 Jan
Distribution of small proteoglycans and glycosaminoglycans in humerus-related articular cartilage of chickens.
2005 Mar
Characterisation of a secreted N-acetyl-beta-hexosaminidase from Trichinella spiralis.
2006 Jan
Sequence analyses of fimbriae subunit FimA proteins on Actinomyces naeslundii genospecies 1 and 2 and Actinomyces odontolyticus with variant carbohydrate binding specificities.
2006 May 10
Design, synthesis, and radiosensitizing activities of sugar-hybrid hypoxic cell radiosensitizers.
2008 Jan 15
Patents

Patents

Sample Use Guides

When extremely high doses of N-acetylgalactosamine are given to experimental animals, a type of hepatitis is created. It is speculated that as much as 280 mg. twice a day would be safe for a healthy 150-pound adult.
Route of Administration: Oral
Rats alimentary tract was used for activity evaluation. After perfusion, the alimentary tract was removed quickly and immersion-fixed in cold PLP for 24 hr at 4C. The tissue blocks were quickly frozen according to the method of Barthel and Raymond. The 4-mkm-thick sections were cut with a Coldtome HM505E (Carl Zeiss, Jena, Germany) and placed on slide glasses precoated with 0.2% 3-aminopropyltriethoxysilane (Shin- Etsu Chemical Co., Tokyo, Japan). Sections were immersed in absolute methanol for 30 min and 0.5% H2O2 for 30 min, followed by treatment with 1.0% normal wild bullfrog serum for 1 hr at r.t. After reaction with 21 biotinylated lectins (Vector Laboratories, Burlingame, U.S.A.) at concentrations of 0.63–2.50 mkg/ml for 16 hr at 4C, the sections were incubated with peroxidase-conjugated streptavidin (diluted to 1:500; Dako, Glostrup, Denmark) for 1 hr at r.t. These sections were then reacted with 3, 3’-diaminobenzideine (Dojindo Lab., Kumamoto, Japan) containing 0.03% H2O2 and were counterstained with methyl green. The specificity of each lectin was confirmed by pretreatment of the lectin solution containing the appropriate sugars (β-N-Acetyl-D-galactosamine, beta-D-GalNAc 1.25mkg/ml) to inhibit lectin binding. Sections were also incubated in the streptavidin solution or phosphate buffer alone.
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:22:40 GMT 2023
Edited
by admin
on Fri Dec 15 18:22:40 GMT 2023
Record UNII
KM15WK8O5T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
.BETA.-N-ACETYL-D-GALACTOSAMINE
Common Name English
2-DEOXY-2-ACETAMIDO-.BETA.-D-GALACTOPYRANOSE
Systematic Name English
GALACTOPYRANOSE, 2-ACETAMIDO-2-DEOXY-, .BETA.-D-
Systematic Name English
.BETA.-D-GALACTOPYRANOSE, 2-(ACETYLAMINO)-2-DEOXY-
Systematic Name English
N-ACETYL-.BETA.-D-GALACTOSAMINE
Common Name English
.BETA.-D-N-ACETYLGALACTOSAMINE
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
217-321-9
Created by admin on Fri Dec 15 18:22:40 GMT 2023 , Edited by admin on Fri Dec 15 18:22:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID601260928
Created by admin on Fri Dec 15 18:22:40 GMT 2023 , Edited by admin on Fri Dec 15 18:22:40 GMT 2023
PRIMARY
PUBCHEM
440552
Created by admin on Fri Dec 15 18:22:40 GMT 2023 , Edited by admin on Fri Dec 15 18:22:40 GMT 2023
PRIMARY
CAS
14131-60-3
Created by admin on Fri Dec 15 18:22:40 GMT 2023 , Edited by admin on Fri Dec 15 18:22:40 GMT 2023
PRIMARY
FDA UNII
KM15WK8O5T
Created by admin on Fri Dec 15 18:22:40 GMT 2023 , Edited by admin on Fri Dec 15 18:22:40 GMT 2023
PRIMARY