ChemicalBook--->CAS DataBase List--->1396640-59-7

1396640-59-7

1396640-59-7 Structure

1396640-59-7 Structure
IdentificationBack Directory
[Name]

Rezafungin
[CAS]

1396640-59-7
[Synonyms]

SP-3025
Rezafungin
[Molecular Formula]

C63H85N8O17
[MDL Number]

MFCD34593622
[MOL File]

1396640-59-7.mol
[Molecular Weight]

1226.41
Chemical PropertiesBack Directory
[InChIKey]

LNFCWEXGZIEGJW-WIQSWMFQNA-O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Description]

Rezafungin is a novel, once-weekly antifungal being developed for the treatment and prevention of serious fungal infections.Rezafungin is a member of the echinocandin class of drugs. Echinocandins are considered the safest antifungal drugs available and are suggested by the Infectious Disease Society of America (IDSA) as first-line treatment for fungal infections. 
[Uses]

Rezafungin (CD-101) is a second generation echinocandin with a similar spectrum and mechanism of action. Along with fosmanogepix, ibrexafungerp, olorofim, and opelconazole, rezafungin heralds a new era in the treatment of fungal infections.
[Side effects]

Adverse effects associated with the use of Rezzayo may include, but are not limited to, the following: hypokalemia, pyrexia, diarrhea, anemia, vomiting, nausea, hypomagnesemia, abdominal pain, constipation, and hypophosphatemia.
[Mechanism of action]

Rezafungin is a semi-synthetic echinocandin. Rezafungin inhibits the 1,3-B-D-glucan synthase enzyme complex, which is present in fungal cell walls but not in mammalian cells. This results in the inhibition of the formation of 1,3-B-D-glucan, an essential component of the fungal cell wall of many fungi, including Candida species (spp.). Inhibition of 1,3-B-D-glucan synthesis results in concentration-dependent in vitro fungicidal activity against Candida spp., however, the clinical significance of this activity is unknown.
[in vivo]

Rezafungin (Biafungin) shows potent in vivo efficacy as prophylaxis against Pneumocystis in a mouse infection model[1].

Animal Model:C3H/HeN mice[1]
Dosage:1 mg/kg
Administration:Intraperitoneal injection; once daily for 6 days
Result:Significantly reduced nuclei and asci burdens.
[References]

[1] Syed, Yahiya Y. “Rezafungin: First Approval.” Drugs 83 9 (2023): 833–840.
[2] Desnos-Ollivier, Marie and Fanny Lanternier. “New antifungals development: rezafungin in candidiasis treatment.” Lancet Infectious Diseases 22 3 (2023).
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