Compounds > 4-methylumbelliferyl-n,n-diacetylchitobioside
Page last updated: 2024-11-08

4-methylumbelliferyl-n,n-diacetylchitobioside

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

Cross-References

ID SourceID
PubMed CID171284
MeSH IDM0104774

Synonyms (37)

Synonym
4-methyl-umbelliferyl-n-acetyl-chitobiose
DB02759
4-mudacb
4-methylumbelliferyl-n,n-diacetylchitobioside
4-methylumbelliferyl di-n-acetyl-|a-d-chitobiose
n-[(2s,3r,4r,5s,6r)-2-[(2r,3s,4r,5r,6s)-5-acetamido-4-hydroxy-2-(hydroxymethyl)-6-(4-methyl-2-oxochromen-7-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
53643-12-2
4-methylumbelliferyl beta-d-n,n'-diacetylchitobioside
syw68vg2t6 ,
2h-1-benzopyran-2-one, 7-((2-(acetylamino)-4-o-(2-(acetylamino)-2-deoxy-beta-d-glucopyranosyl)-2-deoxy-beta-d-glucopyranosyl)oxy)-4-methyl-
unii-syw68vg2t6
AKOS015897096
4-methylumbelliferyl beta-d-n,n-diacetylchitobiose
4mu-nag2, sigma
n-[(2s,3r,4r,5s,6r)-2-{[(2r,3s,4r,5r,6s)-5-acetamido-4-hydroxy-2-(hydroxymethyl)-6-[(4-methyl-2-oxo-2h-chromen-7-yl)oxy]oxan-3-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
bdbm10848
fluorogenic substrate
n,n'-diacetyl-4-methylumbelliferyl-beta-d-chitobioside
DTXSID30201881
4-methylumbelliferyl beta-d-n,n'-diacetylchitobioside hydrate
4-methyl-2-oxo-2h-chromen-7-yl 2-(acetylamino)-4-o-[2-(acetylamino)-2-deoxy-beta-d-glucopyranosyl]-2-deoxy-beta-d-glucopyranoside
4-methylumbelliferyl n,n'-diacetyl-|a-chitobioside
4-methylumbelliferyl di-n-acetyl-beta-d-chitobiose
n-((2s,3r,4r,5s,6r)-5-((2s,3r,4r,5s,6r)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yloxy)-4-hydroxy-6-(hydroxymethyl)-2-(4-methyl-2-oxo-2h-chromen-7-yloxy)tetrahydro-2h-pyran-3-yl)acetamide
4-methylumbelliferyl beta-d-n,n'-diacetyl-chitobioside
Q27460928
4-methylumbelliferyl n,n-diacetyl--d-chitobioside
4-methylumbelliferyl di-n-acetyl-?-d-chitobiose
4-methylumbelliferyl-n,n'-diacetyl-beta-d-chitobioside
4-methylumbelliferyl beta -d-n,n'-diacetylchitobioside
4-methylumbelliferyl n,n'-diacetyl-.beta.-chitobioside
n-((2r,3r,4r,5s,6s)-2-((2r,3r,4s,5s,6s)-5-acetamido-2-(hydroxymethyl)-6-(4-methyl-2-oxidanylidene-chromen-7-yl)oxy-4-oxidanyl-oxan-3-yl)oxy-6-(hydroxymethyl)-4,5-bis(oxidanyl)oxan-3-yl)ethanamide
4-methylumbelliferyl .beta.-d-nn'-diacetylchitobioside
7-((2-(acetylamino)-4-o-(2-(acetylamino)-2-deoxy-.beta.-d-glucopyranosyl)-2-deoxy-.beta.-d-glucopyranosyl)oxy)-4-methyl-2h-1-benzopyran-2-one
n-((2s,3r,4r,5s,6r)-5-(((2s,3r,4r,5s,6r)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy)-4-hydroxy-6-(hydroxymethyl)-2-((4-methyl-2-oxo-2h-chromen-7-yl)oxy)oxan-3-yl)acetamide
methylumbelliferyl-n,n'-diacetylchitobioside
PD060002
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (14.29)18.7374
1990's3 (42.86)18.2507
2000's2 (28.57)29.6817
2010's1 (14.29)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: 12.57

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.57 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.65 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.57)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
1-anilino-8-naphthalenesulfonate
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd. 8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.		1.9810aminonaphthalene;
naphthalenesulfonic acid		fluorescent probe
guanidine
Guanidine: A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.. guanidine : An aminocarboxamidine, the parent compound of the guanidines.		2.6730carboxamidine;
guanidines;
one-carbon compound
acetylglucosamine
Acetylglucosamine: The N-acetyl derivative of glucosamine.. N-acetyl-beta-D-glucosamine : An N-acetyl-D-glucosamine having beta-configuration at the anomeric centre.		2.0110N-acetyl-D-glucosamineepitope
iodine
[no description available]		1.9810halide anion;
monoatomic iodine		human metabolite
4-methylumbelliferyl 2-acetamido-2-deoxy-beta-d-glucopyranoside
4-methylumbelliferyl 2-acetamido-2-deoxy-beta-D-glucopyranoside: RN given refers to (beta)-isomer		2.0110
chitotriose
chitotriose : An amino trisaccharide comprising of three 2-amino-2-deoxy-D-glucopyranose units joined by beta-(1->4) linkages.		2.0110
glucosamine
D-glucosamine : An amino sugar whose structure comprises D-glucose having an amino substituent at position 2.. 2-amino-2-deoxy-D-glucopyranose : A D-glucosamine whose structure comprises D-glucopyranose having an amino substituent at position 2.		2.0110D-glucosamineEscherichia coli metabolite;
geroprotector;
mouse metabolite
hymecromone
Hymecromone: A coumarin derivative possessing properties as a spasmolytic, choleretic and light-protective agent. It is also used in ANALYTICAL CHEMISTRY TECHNIQUES for the determination of NITRIC ACID.		3.3870hydroxycoumarinantineoplastic agent;
hyaluronic acid synthesis inhibitor
chitosan
[no description available]		2.0110
muramidase
Muramidase: A basic enzyme that is present in saliva, tears, egg white, and many animal fluids. It functions as an antibacterial agent. The enzyme catalyzes the hydrolysis of 1,4-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrin. EC 3.2.1.17.		2.8940
ConditionIndicatedRelationship StrengthStudiesTrials