1-[(4R,5R)-4,5-Dihydroxy-L-ornithine]echinocandin B hydrochloride

  • Product Code: 73963
  CAS:    1029890-89-8
Molecular Weight: 834.27 g./mol Molecular Formula: C₃₄H₅₂ClN₇O₁₅
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry, sealed
Product Description: Primarily used as an antifungal agent, this compound is effective against a range of fungal infections, particularly those caused by Candida and Aspergillus species. It works by inhibiting the synthesis of beta-(1,3)-D-glucan, an essential component of the fungal cell wall, leading to cell lysis and death. Its application is crucial in treating invasive fungal infections in immunocompromised patients, such as those undergoing chemotherapy or organ transplantation. Additionally, it is utilized in research settings to study fungal cell wall biosynthesis and the mechanisms of antifungal resistance. Its hydrochloride form enhances solubility, making it more suitable for intravenous administration in clinical settings.
Product Specification:
Test Specification
APPEARANCE White to Off-White Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days ฿9,880.00
+
-
0.050 10-20 days ฿24,700.00
+
-
0.250 10-20 days ฿63,700.00
+
-
1-[(4R,5R)-4,5-Dihydroxy-L-ornithine]echinocandin B hydrochloride
Primarily used as an antifungal agent, this compound is effective against a range of fungal infections, particularly those caused by Candida and Aspergillus species. It works by inhibiting the synthesis of beta-(1,3)-D-glucan, an essential component of the fungal cell wall, leading to cell lysis and death. Its application is crucial in treating invasive fungal infections in immunocompromised patients, such as those undergoing chemotherapy or organ transplantation. Additionally, it is utilized in research settings to study fungal cell wall biosynthesis and the mechanisms of antifungal resistance. Its hydrochloride form enhances solubility, making it more suitable for intravenous administration in clinical settings.
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