Natural Products from Rubia cordifolia

Natural Products Isolated from Rubia cordifolia

BioCrick provides high-purity natural products and bioactive compounds isolated and purified from natural sources for scientific research.

  • Natural product compounds selected from diverse chemical and biological sources.
  • Broad structural diversity and coverage of biological activities.
  • Product activity information can be supported by published literature, patents and research reports.
  • Natural products can be selected according to source, target, activity and disease research interests.
  • Compounds should be stored according to the product specifications after receipt.
Natural products isolated from Rubia cordifolia
Natural products isolated from Rubia cordifolia

Natural Products from Rubia cordifolia

20 natural product s associated with Rubia cordifolia

Natural products and bioactive compounds from Rubia cordifolia
Catalog No. Product Name CAS Number COA
BCN6384 1,3,6-Trihydroxy-2-methylanthraquinone 3-O-(6'-O-acetyl)-alpha-L-rhamnosyl-(1->2)-Beta-D-glucoside
1,3,6-Trihydroxy-2-methylanthraquinone 3-O-(6'-O-acetyl)-alpha-L-rhamnosyl-(1->2)-Beta-D-glucoside chemical structure
87686-87-1 COA
BCN8732 1,3,6-Trihydroxy-2-methylanthraquinone 3-O-alpha-L-rhamnosyl-(1->2)-beta-D-glucoside
1,3,6-Trihydroxy-2-methylanthraquinone 3-O-alpha-L-rhamnosyl-(1->2)-beta-D-glucoside chemical structure
87686-88-2 COA
BCN6375 1,4-Dihydroxy-2-carbomethoxy-3-prenylnaphthalene-1-O-beta-glucopyranoside
1,4-Dihydroxy-2-carbomethoxy-3-prenylnaphthalene-1-O-beta-glucopyranoside chemical structure
1415729-43-9 COA
BCN3478 1-Hydroxy-2-methylanthraquinone
1-Hydroxy-2-methylanthraquinone chemical structure
6268-09-3 COA
BCN8571 2-Amino-3-carboxy-1,4-naphthoquinone
2-Amino-3-carboxy-1,4-naphthoquinone chemical structure
173043-38-4 COA
BCN9074 3-(β-D-Glucopyranosyloxy)-1,6-dihydroxy-2-methyl-9,10-anthracenedione
3-(β-D-Glucopyranosyloxy)-1,6-dihydroxy-2-methyl-9,10-anthracenedione chemical structure
125906-49-2 COA
BCN4425 6-Hydroxyrubiadin
6-Hydroxyrubiadin chemical structure
87686-86-0 COA
BCN3479 Alizarin
Alizarin chemical structure
72-48-0 COA
BCN8247 Dihydromollugin
Dihydromollugin chemical structure
60657-93-4 COA
BCC1709 Lucidin
Lucidin chemical structure
478-08-0 COA
BCN8249 Lucidin 3-O-glucoside
Lucidin 3-O-glucoside chemical structure
22255-29-4 COA
BCN8584 Lucidin 3-O-primeveroside
Lucidin 3-O-primeveroside chemical structure
29706-59-0 COA
BCN7597 Methyl 1,4-bisglucosyloxy-3-prenyl-2-naphthoate
Methyl 1,4-bisglucosyloxy-3-prenyl-2-naphthoate chemical structure
90685-26-0 COA
BCN5742 Mollugin
Mollugin chemical structure
55481-88-4 COA
BCN3477 Purpurin
Purpurin chemical structure
81-54-9 COA
BCN6047 Rubiadin
Rubiadin chemical structure
117-02-2 COA
BCN8588 Rubiayannone A
Rubiayannone A chemical structure
517978-25-1 COA
BCN3511 Rubinaphthin A
Rubinaphthin A chemical structure
448962-05-8 COA
BCN7871 Rubioncolin C
Rubioncolin C chemical structure
132242-52-5 COA
BCN8601 Rubipodanone A
Rubipodanone A chemical structure
2170211-22-8 COA

References

ISSR Characterization and Quantification of Purpurin and Alizarin in Rubia cordifolia L. Populations from India.[Pubmed: 30039443]


Rubia cordifolia L., is an industrially viable medicinal crop and is widely exploited for the therapeutic potential of its bioactive metabolite, purpurin. The present investigation aimed to explore the chemotypic and molecular variability in seven wild populations of R. cordifolia from South Eastern Ghats region of India. Thirty-eight individuals were assessed for molecular fingerprinting (ISSR markers) and densitometric quantification of purpurin and alizarin. The populations of Yelagiri Hills and Shervaroy Hills contained the highest levels of alizarin (0.115 and 0.093%, respectively) while Pachamalai and Kolli Hills revealed the highest purpurin content (0.284 and 0.280%, respectively). Genetic diversity was generally higher in the same populations that produced higher metabolite content, with the exception of Pachamalai, suggesting a highly prioritized conservation concern. The study revealed a Nei's total gene diversity at species level of 0.266 and of 0.187 at population level, with an average population genetic differentiation of 0.28. No clear genetic or chemical structure was retrieved between the studied populations, with individuals from different locations clustering together, and no significant correlation was obtained between metabolites and genetic diversity or between these and the populations' geographic distances.