1. Anti-infection
  2. Fungal
  3. CHNQD-02204

CHNQD-02204 is a potent and selective antifungal agent with in vitro activity against Candida albicans, with a MIC of 0.025 μg/mL. CHNQD-02204 inhibits ergosterol biosynthesis, disrupts the membrane integrity and biofilm formation of Candida albicans, and suppresses the morphological transition of Candida albicans from yeast to hyphal form. CHNQD-02204 can be used in studies related to candidal infections.

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CHNQD-02204

CHNQD-02204 Chemical Structure

CAS No. : 3094676-22-6

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Description

CHNQD-02204 is a potent and selective antifungal agent with in vitro activity against Candida albicans, with a MIC of 0.025 μg/mL. CHNQD-02204 inhibits ergosterol biosynthesis, disrupts the membrane integrity and biofilm formation of Candida albicans, and suppresses the morphological transition of Candida albicans from yeast to hyphal form. CHNQD-02204 can be used in studies related to candidal infections[1].

In Vitro

CHNQD-02204 (0.05 μg/mL; 2 h) disrupts the cell surface integrity of Candida albicans ATCC 10231, leading to cell shrinkage and indentation[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Parmacokinetics
Species Dose Route T1/2 Tmax Cmax AUC0-t AUC0-∞ CL
Rat[1] 2.5 mg/kg i.v. 12.7 min 1 min 5952.5 ng/mL 31896.7 min·ng/mL 46463.1 min·ng/mL 53.8 mL/min/kg
In Vivo

CHNQD-02204 (2.5 mg/kg; intravenous injection; administered 3 times) reduces the fungal burden in the spleen, lung and kidney of immunocompromised mice with candidiasis[1].
CHNQD-02204 (2.5 mg/kg; intravenous injection; twice daily; for 3 consecutive days) reduces the fungal burden in the spleen, lung and kidney of immunocompromised mice with disseminated candidiasis, and alleviates infection-induced body weight loss[1].
CHNQD-02204 (10 mg/kg; intravenous injection; single administration) is well tolerated in healthy female C57BL/6J mice, with no mortality, body weight changes or histopathological abnormalities observed within 7 days[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: ICR (female, 6-week-old, 24-26 g, immunocompromised via intraperitoneal cyclophosphamide injection)[1]
Dosage: 2.5 mg/kg
Administration: i.v.; three doses at 2, 6, and 10 h post-infection
Result: Reduced fungal burden in the spleen by 0.40 log10 CFU compared with the infected control group.
Reduced fungal burden in the lung by 0.29 log10 CFU compared with the infected control group.
Reduced fungal burden in the kidney by 0.62 log10 CFU compared with the infected control group.
Animal Model: ICR (female, 6-week-old, 24-26 g, immunocompromised via intraperitoneal cyclophosphamide injection)[1]
Dosage: 2.5 mg/kg
Administration: i.v.; twice daily; 3 consecutive days
Result: Reduced fungal burden in the spleen by 0.37 log10 CFU compared with the infected control group.
Reduced fungal burden in the lung by 0.78 log10 CFU compared with the infected control group.
Reduced fungal burden in the kidney by 0.41 log10 CFU compared with the infected control group.
Marked reduction of fungal content in multiple organs, with almost no fungal growth observed in the lungs via periodic acid-Schiff staining.
Mitigated weight loss induced by fungal infection during the 3-day treatment period.
Molecular Weight

517.31

Formula

C25H18Cl2O8

CAS No.
SMILES

ClC(C=CC=C1)=C1C(OC2=C(Cl)C=CC=C2C3=C(OC)C(C4=C(O)C=C(OC)C(OC)=C4O3)=O)=O

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CHNQD-02204
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HY-183333
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