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Catalog Number:
05906
CAS Number:
123314-39-6
L-Citrulline 7-amido-4-methylcoumarin hydrobromide
Synonym(s):
L-Cit-AMC·HBr, (S-2-Amino-5-ureidopentanoic acid 7-amido-4-methylcoumarinhydrobromide, H-Cit-AMC·HBr
Documents
$402.50 /25MG
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Product Information

L-Citrulline 7-amido-4-methylcoumarin hydrobromide is a versatile compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound serves as a valuable tool in the study of nitric oxide synthesis and has been utilized in various assays to evaluate enzyme activity, particularly in the context of arginine metabolism. Its unique structure allows for effective interaction with biological systems, making it an ideal candidate for researchers focused on cardiovascular health and metabolic studies.

In addition to its research applications, L-Citrulline 7-amido-4-methylcoumarin hydrobromide has potential uses in drug formulation, particularly in the development of therapeutics aimed at enhancing blood flow and reducing fatigue. Its ability to act as a substrate for specific enzymes opens avenues for innovative treatments in sports medicine and geriatric care. Researchers and industry professionals can leverage this compound to explore new therapeutic pathways, making it a significant addition to any laboratory focused on health and wellness.

Synonyms
L-Cit-AMC·HBr, (S-2-Amino-5-ureidopentanoic acid 7-amido-4-methylcoumarinhydrobromide, H-Cit-AMC·HBr
CAS Number
123314-39-6
Molecular Formula
C16H20N4O4·HBr
Molecular Weight
413.26
MDL Number
MFCD00152040
PubChem ID
71433869
Conditions
Store at 0-8°C
General Information
Synonyms
L-Cit-AMC·HBr, (S-2-Amino-5-ureidopentanoic acid 7-amido-4-methylcoumarinhydrobromide, H-Cit-AMC·HBr
CAS Number
123314-39-6
Molecular Formula
C16H20N4O4·HBr
Molecular Weight
413.26
MDL Number
MFCD00152040
PubChem ID
71433869
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L-Citrulline 7-amido-4-methylcoumarin hydrobromide is widely utilized in research focused on:

  • Biochemical Research: This compound is often used as a substrate in studies examining enzyme activity, particularly in the context of nitric oxide synthesis and metabolic pathways.
  • Pharmaceutical Development: It plays a role in the formulation of drugs aimed at enhancing cardiovascular health by improving blood flow and reducing blood pressure.
  • Nutrition Science: Researchers explore its potential benefits in sports nutrition, particularly for its ability to enhance exercise performance and recovery through improved blood circulation.
  • Diagnostic Applications: The compound is investigated for use in diagnostic assays that measure enzyme activity related to certain metabolic disorders, offering insights into patient health.
  • Cosmetic Formulations: Its properties are leveraged in skin care products for their potential to improve skin hydration and elasticity, making it appealing for cosmetic chemists.

Citations