MedKoo Cat#: 318300 | Name: Nalidixic Acid
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Nalidixic Acid is the first of the synthetic quinolone antibiotics. Nalidixic acid is effective primarily against gram-negative bacteria, with minor anti-gram-positive activity. In lower concentrations, it acts in a bacteriostatic manner; that is, it inhibits growth and reproduction. In higher concentrations, it is bactericidal, meaning that it kills bacteria instead of merely inhibiting their growth.

Chemical Structure

Nalidixic Acid
Nalidixic Acid
CAS#389-08-2

Theoretical Analysis

MedKoo Cat#: 318300

Name: Nalidixic Acid

CAS#: 389-08-2

Chemical Formula: C12H12N2O3

Exact Mass: 232.0848

Molecular Weight: 232.24

Elemental Analysis: C, 62.06; H, 5.21; N, 12.06; O, 20.67

Price and Availability

Size Price Availability Quantity
10g USD 150.00
100g USD 450.00
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Synonym
Nalidixic Acid, Nevigramon, Neggram, Wintomylon, WIN 18,320
IUPAC/Chemical Name
1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid
InChi Key
MHWLWQUZZRMNGJ-UHFFFAOYSA-N
InChi Code
InChI=1S/C12H12N2O3/c1-3-14-6-9(12(16)17)10(15)8-5-4-7(2)13-11(8)14/h4-6H,3H2,1-2H3,(H,16,17)
SMILES Code
O=C(C1=CN(CC)C2=C(C=CC(C)=N2)C1=O)O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO, not in water
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
Nalidixic acid, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria.
In vitro activity:
Sodium nalidixate inhibited the cell growth and division of several respiratory competent strains of Saccharomyces cerevisiae. Reference: Mol Gen Genet. 1976 Jul 5;146(1):95-100. https://pubmed.ncbi.nlm.nih.gov/785214/
In vivo activity:
Nalidixic acid preferentially suppressed growth in soft agar of transformed Balb/3T3 mouse cells induced by methylcholanthrene. Nalidixic acid suppressed growth in soft agar of NIH/3T3 mouse cells transformed by an activated c-Ha-ras, without affecting the amount of ras p21 proteins as detected by an immunoblotting analysis using a monoclonal antibody. Reference: Br J Cancer. 1989 Dec;60(6):880-6. https://pubmed.ncbi.nlm.nih.gov/2690912/
Solvent mg/mL mM
Solubility
DMSO 6.0 25.84
Water 5.0 21.53
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 232.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
1. Chadha J, Khullar L. Subinhibitory concentrations of nalidixic acid alter bacterial physiology and induce anthropogenic resistance in a commensal strain of Escherichia coli in vitro. Lett Appl Microbiol. 2021 Nov;73(5):623-633. doi: 10.1111/lam.13550. Epub 2021 Aug 24. PMID: 34376018. 2. Carnevali F, Sarcoe LE, Whittaker PA. Differential effects of nalidixate on the cell growth of respiratory competent strains and cytoplasmic petite mutants of Saccharomyces cerevisiae. Mol Gen Genet. 1976 Jul 5;146(1):95-100. doi: 10.1007/BF00267988. PMID: 785214. 3. Kaneko M, Horikoshi J. Reversible suppression by nalidixic acid of anchorage-independent growth of mouse cells transformed by 3-methylcholanthrene or an activated c-Ha-ras gene. Br J Cancer. 1989 Dec;60(6):880-6. doi: 10.1038/bjc.1989.384. PMID: 2690912; PMCID: PMC2247252. 4. McQueen CA, Rosado RR, Williams GM. Effect of nalidixic acid on DNA repair in rat hepatocytes. Cell Biol Toxicol. 1989 Jun;5(2):201-6. doi: 10.1007/BF00122653. PMID: 2504447.
In vitro protocol:
1. Chadha J, Khullar L. Subinhibitory concentrations of nalidixic acid alter bacterial physiology and induce anthropogenic resistance in a commensal strain of Escherichia coli in vitro. Lett Appl Microbiol. 2021 Nov;73(5):623-633. doi: 10.1111/lam.13550. Epub 2021 Aug 24. PMID: 34376018. 2. Carnevali F, Sarcoe LE, Whittaker PA. Differential effects of nalidixate on the cell growth of respiratory competent strains and cytoplasmic petite mutants of Saccharomyces cerevisiae. Mol Gen Genet. 1976 Jul 5;146(1):95-100. doi: 10.1007/BF00267988. PMID: 785214.
In vivo protocol:
1. Kaneko M, Horikoshi J. Reversible suppression by nalidixic acid of anchorage-independent growth of mouse cells transformed by 3-methylcholanthrene or an activated c-Ha-ras gene. Br J Cancer. 1989 Dec;60(6):880-6. doi: 10.1038/bjc.1989.384. PMID: 2690912; PMCID: PMC2247252. 2. McQueen CA, Rosado RR, Williams GM. Effect of nalidixic acid on DNA repair in rat hepatocytes. Cell Biol Toxicol. 1989 Jun;5(2):201-6. doi: 10.1007/BF00122653. PMID: 2504447.
1: Gu B, Cao Y, Pan S, Zhuang L, Yu R, Peng Z, Qian H, Wei Y, Zhao L, Liu G, Tong M. Comparison of the prevalence and changing resistance to nalidixic acid and ciprofloxacin of Shigella between Europe-America and Asia-Africa from 1998 to 2009. Int J Antimicrob Agents. 2012 Jul;40(1):9-17. doi: 10.1016/j.ijantimicag.2012.02.005. Epub 2012 Apr 5. Review. PubMed PMID: 22483324. 2: Shakespeare WA, Davie D, Tonnerre C, Rubin MA, Strong M, Petti CA. Nalidixic acid-resistant Salmonella enterica serotype Typhi presenting as a primary psoas abscess: case report and review of the literature. J Clin Microbiol. 2005 Feb;43(2):996-8. Review. PubMed PMID: 15695728; PubMed Central PMCID: PMC548044. 3: Singh H, Sachdev HP. Nalidixic acid. Indian Pediatr. 1988 Mar;25(3):279-81. Review. PubMed PMID: 3069738. 4: Albrecht R. Development of antibacterial agents of the nalidixic acid type. Prog Drug Res. 1977;21:9-104. Review. PubMed PMID: 339272. 5: Zinsser HH. Nalidixic acid in acute and chronic urinary tract infections. Med Clin North Am. 1970 Sep;54(5):1347-50. Review. PubMed PMID: 4248514. 6: Pagnini G. [Nalidixic acid]. Antibiotica. 1967 Jun;5(2):134-59. Review. Multiple languages. PubMed PMID: 4389549. 7: Parry CM. The treatment of multidrug-resistant and nalidixic acid-resistant typhoid fever in Viet Nam. Trans R Soc Trop Med Hyg. 2004 Jul;98(7):413-22. Review. PubMed PMID: 15138078. 8: Petersen U. [The evolution of quinolone: from nalidixic acid to the quinolones of the third generation]. Pharm Unserer Zeit. 2001;30(5):376-81. Review. German. PubMed PMID: 11575173. 9: Gleckman R, Alvarez S, Joubert DW, Matthews SJ. Drug therapy reviews: nalidixic acid. Am J Hosp Pharm. 1979 Aug;36(8):1071-6. Review. PubMed PMID: 384787. 10: Bauernfeind A. Mode of action of nalidixic acid. Antibiot Chemother (1971). 1971;17:122-36. Review. PubMed PMID: 4950999. 11: Finegold SM, Ziment I. Sulfonamides, nitrofurans and nalidixic acid. Pediatr Clin North Am. 1968 Feb;15(1):95-105. Review. PubMed PMID: 4866909.