Page last updated: 2024-12-06

glucosaminic acid

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Glucosaminic acid, also known as D-glucosaminic acid, is a naturally occurring amino sugar that serves as a precursor in the biosynthesis of hyaluronic acid. It is a derivative of glucose with an amino group replacing the hydroxyl group at position 2. The compound is involved in various biological processes, including cell growth, cartilage formation, and immune function. Research on glucosaminic acid focuses on its potential therapeutic applications in treating osteoarthritis, inflammatory diseases, and other conditions. While it is not a well-studied compound, its potential benefits in promoting joint health and reducing inflammation have attracted considerable interest. Studies have explored the use of glucosaminic acid in combination with other compounds, such as chondroitin sulfate, to enhance its effects. However, further research is needed to establish its safety and efficacy in humans.'

glucosaminic acid: RN given refers to cpd with unspecified isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

2-amino-2-deoxy-D-gluconic acid : Hexanoic acid with four hydroxy groups at C-3, C-4, C-5, C-6, and an amino group at C-2. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID73563
CHEMBL ID3039035
CHEBI ID17784
SCHEMBL ID396940
MeSH IDM0108857

Synonyms (64)

Synonym
gluconic acid, 2-amino-2-deoxy-, d-
nsc 404265
einecs 222-879-1
ai3-51894
nsc 37779
glucosaminic acid
d-gluconic acid, 2-amino-2-deoxy-
KBIO1_001495
DIVK1C_006551
SDCCGMLS-0066564.P001
SPECTRUM5_000432
SPECTRUM4_001866
SPECTRUM_001231
(3r,4s,5r)-3,4,5,6-tetrahydroxy-d-norleucine
2-amino-2-deoxy-d-gluconic acid
CHEBI:17784 ,
BSPBIO_003133
NCGC00178247-01
(2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxy-hexanoic acid
d-glucosaminate
d-glucosaminic acid
glucosaminate ,
C03752
3646-68-2
d-glucosaminic acid, >=98%
KBIO3_002353
KBIOSS_001711
KBIO2_004279
KBIO2_006847
KBIOGR_002334
KBIO2_001711
SPECTRUM2_001910
SPBIO_001880
SPECPLUS_000455
SPECTRUM3_001347
SPECTRUM310298
6BA699D8-74A0-43AF-82A9-F68E6BFA0B50
2-amino-2-deoxygluconic acid
BMSE000440
gluconic acid, 2-amino-2-deoxy-
(2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanoic acid
d-glucosamic acid
G0042
6165-14-6
A823258
AKOS006238367
CCG-38481
chembl3039035 ,
bdbm50442917
SCHEMBL396940
W-202514
mfcd00037764
(2r,3r,4s,5r)-2-azanyl-3,4,5,6-tetrakis(oxidanyl)hexanoic acid
sr-05000002429
SR-05000002429-1
d-?glucosamic acid
HY-128745
Q27102608
CS-0102537
T72366
DTXSID60878848
AS-56887
d-lucosamic acid
(2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanoicacid

Research Excerpts

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
bacterial metaboliteAny prokaryotic metabolite produced during a metabolic reaction in bacteria.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
amino acid zwitterionThe zwitterionic form of an amino acid having a negatively charged carboxyl group and a positively charged amino group.
gluconic acid derivativeA hexonic acid derivative that is formally obtained from gluconic acid.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Solute carrier organic anion transporter family member 1B1Homo sapiens (human)IC50 (µMol)11.74900.05002.37979.7000AID977600
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (9)

Processvia Protein(s)Taxonomy
xenobiotic metabolic processSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
monoatomic ion transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
organic anion transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
bile acid and bile salt transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
prostaglandin transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
heme catabolic processSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
sodium-independent organic anion transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
transmembrane transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
thyroid hormone transportSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (5)

Processvia Protein(s)Taxonomy
organic anion transmembrane transporter activitySolute carrier organic anion transporter family member 1B1Homo sapiens (human)
bile acid transmembrane transporter activitySolute carrier organic anion transporter family member 1B1Homo sapiens (human)
prostaglandin transmembrane transporter activitySolute carrier organic anion transporter family member 1B1Homo sapiens (human)
sodium-independent organic anion transmembrane transporter activitySolute carrier organic anion transporter family member 1B1Homo sapiens (human)
thyroid hormone transmembrane transporter activitySolute carrier organic anion transporter family member 1B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (4)

Processvia Protein(s)Taxonomy
plasma membraneSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
basal plasma membraneSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
membraneSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
basolateral plasma membraneSolute carrier organic anion transporter family member 1B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID977600pIC50 values for sodium fluorescein (10 uM) uptake in OATP1B1-transfected CHO cells2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-199011 (35.48)18.7374
1990's3 (9.68)18.2507
2000's9 (29.03)29.6817
2010's8 (25.81)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 25.17

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index25.17 (24.57)
Research Supply Index3.53 (2.92)
Research Growth Index4.69 (4.65)
Search Engine Demand Index29.80 (26.88)
Search Engine Supply Index2.70 (0.95)

This Compound (25.17)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (9.09%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other30 (90.91%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]