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    Fluconazole

    Available from stock

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      Fluconazole

      SKU
      F0104

      Category: Antibiotics

      Synonyms
      2-(2,4-Difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol, UK 49858, Diflucan
      86386-73-4
      CAS-Number
      C13H12F2N6O
      Molecular Formula
      306.27
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White crystalline powder
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in DMSO (10mg/ml), ethanol (10mg/ml), methanol or acetone.
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Hazard statements
      H302 - H360D - H362 - H412
      Precautionary statements
      P202 - P260 - P263 - P273 - P301 + P312 - P308 + P313
      GHS Symbol
      GHS07+GHS08
      Signal word
      Danger
      Transportation
      Not dangerous goods
      Description
      Fluconazole is a triazole broad-spectrum antifungal agent which is effective against most Candida spp., cryptococcus neoformans and dermatophytes. Fluconazole is an inhibitor of CYP2C19, CYP2C9 and CYP3A4. Fluconazole functions by suppressing the production of ergosterol, a vital constituent of the fungal cell membrane. By impeding ergosterol synthesis, the integrity of the fungal cell membrane is compromised, ultimately resulting in fungal death. Moreover, Fluconazole hinders the activity of cytochrome P450 enzymes.
      Smiles
      FC1=CC(F)=C(C(CN2C=NC=N2)(O)CN3N=CN=C3)C=C1
      InChi Key
      RFHAOTPXVQNOHP-UHFFFAOYSA-N
      References
      (1) M.S. Saag & W.E. Dismukes; Antimicrob. Agents Chemother. 32, 1 (1988) , (2) H. Washton; Diagn. Microbiol. Infect. Dis. 12, 229S (1989) , (3) D.W. Warnock; J. Antimicrob. Chemother. 24, 275 (1989) , (4) K. Richardson, et al.; Rev. Infect. Dis. 12, S267 (1990) , (5) S.F. Kowalsky & D.M. Dixon; Clin. Pharm. 10, 179 (1991) , (6) J.D. Morrow; Am. J. Med. Sci. 302, 129 (1991) , (7) C.M. Perry, et al.; Drugs 49, 984 (1995) , (8) M.V. Martin; J. Antimicrob. Chemother. 44, 429 (1999) , (9) N. Thamban Chandrika, et al.; Bioorg. Med. Chem. 26, 573 (2018) , (10) S. Nami, et al.; Biomed. Pharmacother. 110, 857 (2019) , (11) X. Heng, et al.; Antimicrob. Agents Chemother. 65, e02552 (2021) , (12) M.A Elzoheiry, et al.; Exp. Parasitol. 239, 108291 (2022)
      InChi
      InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2

      Fluconazole is a triazole broad-spectrum antifungal agent which is effective against most Candida spp., cryptococcus neoformans and dermatophytes. Fluconazole is an inhibitor of CYP2C19, CYP2C9 and CYP3A4. Fluconazole functions by suppressing the production of ergosterol, a vital constituent of the fungal cell membrane. By impeding ergosterol synthesis, the integrity of the fungal cell membrane is compromised, ultimately resulting in fungal death. Moreover, Fluconazole hinders the activity of cytochrome P450 enzymes.

      SKU: F0104 Category: Antibiotics
      • Additional information

      Additional information

      Synonyms

      2-(2,4-Difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol, UK 49858, Diflucan

      Purity

      ≥98% (HPLC)

      Appearance

      White crystalline powder

      CAS-Number

      86386-73-4

      Molecular Formula

      C13H12F2N6O

      Molecular Weight

      306.27

      Identity

      1H-NMR

      Solvents

      Soluble in DMSO (10mg/ml), ethanol (10mg/ml), methanol or acetone.

      Smiles

      FC1=CC(F)=C(C(CN2C=NC=N2)(O)CN3N=CN=C3)C=C1

      InChi Key

      RFHAOTPXVQNOHP-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Hazard statements

      H302 – H360D – H362 – H412

      Precautionary statements

      P202 – P260 – P263 – P273 – P301 + P312 – P308 + P313

      GHS Symbol

      GHS07+GHS08

      Signal word

      Danger

      Transportation

      Not dangerous goods

      References

      (1) M.S. Saag & W.E. Dismukes; Antimicrob. Agents Chemother. 32, 1 (1988), (2) H. Washton; Diagn. Microbiol. Infect. Dis. 12, 229S (1989), (3) D.W. Warnock; J. Antimicrob. Chemother. 24, 275 (1989), (4) K. Richardson, et al.; Rev. Infect. Dis. 12, S267 (1990), (5) S.F. Kowalsky & D.M. Dixon; Clin. Pharm. 10, 179 (1991), (6) J.D. Morrow; Am. J. Med. Sci. 302, 129 (1991), (7) C.M. Perry, et al.; Drugs 49, 984 (1995), (8) M.V. Martin; J. Antimicrob. Chemother. 44, 429 (1999), (9) N. Thamban Chandrika, et al.; Bioorg. Med. Chem. 26, 573 (2018), (10) S. Nami, et al.; Biomed. Pharmacother. 110, 857 (2019), (11) X. Heng, et al.; Antimicrob. Agents Chemother. 65, e02552 (2021), (12) M.A Elzoheiry, et al.; Exp. Parasitol. 239, 108291 (2022)

      InChi

      InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2

      Quantity

      500 mg, 1 g, Bulk

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