Page last updated: 2024-12-08

lac dye

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

Description

lac dye: possible food coloring agent which is completely nontoxic at low doses; lac dye is water soluble constituent of stick lac (commercial lac resin); lac resin is hardened secretion of insect Laccifer lacca (lac insect) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

4-{[4-(dimethylamino)phenyl]diazenyl}phenyl-beta-lactoside : A glycoside comprising beta-lactose having a p-(p-dimethylaminophenylazo)phenyl group at the 1-position. [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]

LAC dye : A four-component mixture of dyes obtained from the secretions of the insect species Laccifer lacca. The four components of LAC are laccaic acids A, B, C and D of which laccaic acid A is the most abundant. [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 CID134264
CHEBI ID61710
MeSH IDM0054753

Synonyms (19)

Synonym
lac resin, c.i. natural red 25
glucopyranoside, p-((p-(dimethylamino)phenyl)azo)phenyl 4-o-beta-d-galactopyranosyl-, beta-d-
beta-d-glucopyranoside, 4-((4-(dimethylamino)phenyl)azo)phenyl 4-o-beta-d-galactopyranosyl-
lac dye
p-(p-dimethylaminophenylazo)-phenyl-beta-lactoside
4-(4-dimethylaminophenylazo) beta-lactoside
4-{[4-(dimethylamino)phenyl]diazenyl}phenyl 4-o-beta-d-galactopyranosyl-beta-d-glucopyranoside
4-{[4-(dimethylamino)phenyl]diazenyl}phenyl beta-d-galactopyranosyl-(1->4)-beta-d-glucopyranoside
4-{[4-(dimethylamino)phenyl]diazenyl}phenyl beta-d-galactosyl-(1->4)-beta-d-glucoside
CHEBI:61710 ,
27597-77-9
4-{[4-(dimethylamino)phenyl]diazenyl}phenyl-beta-lactoside
EPITOPE ID:142490
Q27131305
(2s,3r,4s,5r,6r)-2-(((2r,3s,4r,5r,6s)-6-(4-((e)-(4-(dimethylamino)phenyl)diazenyl)phenoxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2h-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol
(2s,3r,4s,5r,6r)-2-[(2r,3s,4r,5r,6s)-6-[4-[[4-(dimethylamino)phenyl]diazenyl]phenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
beta-d-glucopyranoside, 4-[[4-(dimethylamino)phenyl]azo]phenyl 4-o-beta-d-galactopyranosyl-
DTXSID201127805
AKOS040752370

Research Excerpts

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

Roles (1)

RoleDescription
dyenull
[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 (3)

ClassDescription
glycosideA glycosyl compound resulting from the attachment of a glycosyl group to a non-acyl group RO-, RS-, RSe-, etc. The bond between the glycosyl group and the non-acyl group is called a glycosidic bond. By extension, the terms N-glycosides and C-glycosides are used as class names for glycosylamines and for compounds having a glycosyl group attached to a hydrocarbyl group respectively. These terms are misnomers and should not be used. The preferred terms are glycosylamines and C-glycosyl compounds, respectively.
monoazo compoundCompounds containing single -N=N- group.
disaccharide derivativeA carbohydrate derivative that is formally obtained from a disaccharide.
[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]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (9.09)18.7374
1990's2 (9.09)18.2507
2000's4 (18.18)29.6817
2010's9 (40.91)24.3611
2020's5 (22.73)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 41.98

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

MetricThis Compound (vs All)
Research Demand Index41.98 (24.57)
Research Supply Index3.37 (2.92)
Research Growth Index4.98 (4.65)
Search Engine Demand Index60.61 (26.88)
Search Engine Supply Index2.06 (0.95)

This Compound (41.98)

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%
Other28 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]