28587-43-1 Usage
Uses
Used in Pharmaceutical Industry:
7-Geranyloxy-6-methoxycoumarin is used as a potential therapeutic agent for its anti-inflammatory properties, which can help in reducing inflammation and associated symptoms in various conditions.
Used in Antimicrobial Applications:
In the field of microbiology, 7-Geranyloxy-6-methoxycoumarin is used as an antibacterial agent, leveraging its ability to inhibit bacterial growth and potentially combat infections.
Used in Anticancer Research:
7-Geranyloxy-6-methoxycoumarin is used as a subject of study in cancer research due to its potential anticancer activities. It is being investigated for its ability to target and inhibit cancer cell growth, which could lead to the development of new cancer treatments.
Used in Scientific Research:
7-Geranyloxy-6-methoxycoumarin is used as a research compound in various scientific studies aimed at understanding its bioactivity, mechanism of action, and potential applications in different fields, including but not limited to medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 28587-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,8 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28587-43:
(7*2)+(6*8)+(5*5)+(4*8)+(3*7)+(2*4)+(1*3)=151
151 % 10 = 1
So 28587-43-1 is a valid CAS Registry Number.
28587-43-1Relevant academic research and scientific papers
Natural oxyprenylated coumarins are modulators of melanogenesis
Fiorito, Serena,Epifano, Francesco,Preziuso, Francesca,Cacciatore, Ivana,di Stefano, Antonio,Taddeo, Vito Alessandro,de Medina, Philippe,Genovese, Salvatore
, p. 274 - 282 (2018/05/14)
Naturally occurring coumarins 7-isopentenyloxycoumarin, auraptene, and umbelliprenin are able to modulate the biosynthesis of melanin in murine Melan-a cells probably through the interaction with selected biological targets like estrogen receptor β and aryl hydrocarbon receptor. Such a modulation strictly depends on the individual structure of the coumarin: the presence of a 3,3-dimethylallyloxy side chain is a structural determinant for tanning activation whereas a farnesyl one leads to the opposite effect. The parent compound with a free OH group, umbelliferone, did not provide any interaction. Other coumarins assayed, having shorter chains and/or being substituted in other positions, and prenyloxypsoralens, were not active or not further investigated in this context being cytotoxic at low doses.
