Nalidixic acid structure
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Common Name | Nalidixic acid | ||
|---|---|---|---|---|
| CAS Number | 389-08-2 | Molecular Weight | 232.235 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 413.1±45.0 °C at 760 mmHg | |
| Molecular Formula | C12H12N2O3 | Melting Point | 227-229 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 203.6±28.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of Nalidixic acidNalidixic acid is a synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum.Target: AntibacterialNalidixic acid is the first of the synthetic quinolone antibiotics. Nalidixic acid is effective against both gram-positive and gram-negative bacteria. 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. Nalidixic selectively and reversibly blocks DNA replication in susceptible bacteria. Nalidixic acid and related antibiotics inhibit a subunit of DNA gyrase and topoisomerase IV and induce formation of cleavage complexes. It also inhibits the nicking-closing activity on the subunit of DNA gyrase that releases the positive binding stress on the supercoiled DNA. From Wikipedia. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | nalidixic acid |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Nalidixic acid is a synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum.Target: AntibacterialNalidixic acid is the first of the synthetic quinolone antibiotics. Nalidixic acid is effective against both gram-positive and gram-negative bacteria. 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. Nalidixic selectively and reversibly blocks DNA replication in susceptible bacteria. Nalidixic acid and related antibiotics inhibit a subunit of DNA gyrase and topoisomerase IV and induce formation of cleavage complexes. It also inhibits the nicking-closing activity on the subunit of DNA gyrase that releases the positive binding stress on the supercoiled DNA. From Wikipedia. |
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| Related Catalog | |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 413.1±45.0 °C at 760 mmHg |
| Melting Point | 227-229 °C(lit.) |
| Molecular Formula | C12H12N2O3 |
| Molecular Weight | 232.235 |
| Flash Point | 203.6±28.7 °C |
| Exact Mass | 232.084793 |
| PSA | 72.19000 |
| LogP | 1.19 |
| Vapour Pressure | 0.0±1.0 mmHg at 25°C |
| Index of Refraction | 1.605 |
| InChIKey | MHWLWQUZZRMNGJ-UHFFFAOYSA-N |
| SMILES | CCn1cc(C(=O)O)c(=O)c2ccc(C)nc21 |
| Storage condition | 0-6°C |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| Water Solubility | 0.1 G/L (23 ºC) |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Precautionary Statements | P301 + P312 + P330 |
| Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
| Hazard Codes | Xn:Harmful; |
| Risk Phrases | R40;R42/43;R63 |
| Safety Phrases | S22-S36/37-S45-S24 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 2 |
| RTECS | QN2885000 |
| HS Code | 2933990090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 6 | |
|---|---|
| DownStream 1 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
This table lists relevant public references with title, journal and publication metadata for this compound.
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Brucella abortus depends on pyruvate phosphate dikinase and malic enzyme but not on Fbp and GlpX fructose-1,6-bisphosphatases for full virulence in laboratory models.
J. Bacteriol. 196(16) , 3045-57, (2014) The brucellae are the etiological agents of brucellosis, a worldwide-distributed zoonosis. These bacteria are facultative intracellular parasites and thus are able to adjust their metabolism to the ex... |
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Recovery of Pseudomonas aeruginosa culturability following copper- and chlorine-induced stress.
FEMS Microbiol. Lett. 356(2) , 226-34, (2014) This study investigated how quickly cells of the opportunistic pathogen Pseudomonas aeruginosa recover culturability after exposure to two of the most common environmental stressors present in drinkin... |
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Intestinal Epithelial Cell Tyrosine Kinase 2 Transduces IL-22 Signals To Protect from Acute Colitis.
J. Immunol. 195 , 5011-24, (2015) In the intestinal tract, IL-22 activates STAT3 to promote intestinal epithelial cell (IEC) homeostasis and tissue healing. The mechanism has remained obscure, but we demonstrate that IL-22 acts via ty... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| uriben |
| EINECS 206-864-7 |
| uroman |
| uropan |
| NegGram |
| NOGRAM |
| WIN-18320 |
| nalidixic acid |
| Urisal |
| nalix |
| 1-Ethyl-7-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid |
| Ethyl-7-methyl-1,8-naphthyridin-4-one-3-carboxylic Acid |
| 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid |
| T66 BV EN GNJ CVQ E2 H1 |
| poleon |
| negram |
| WINTOMYLON |
| cybis |
| uroneg |
| MFCD00006884 |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What are the upstream materials of nalidixic acid? |
| A: Related upstream materials(CAS) of nalidixic acid: 34748-19-1;33331-59-8;1824-81-3;13250-95-8;13250-96-9;174814-96-1. |
| Q: What is the safety information for nalidixic acid? |
| A: Safety information for nalidixic acid: S22-S36/37-S45-S24. |
| Q: What is the SMILES notation of nalidixic acid? |
| A: SMILES notation of nalidixic acid is CCn1cc(C(=O)O)c(=O)c2ccc(C)nc21. |
| Q: What is the English name of nalidixic acid? |
| A: The English name of nalidixic acid is nalidixic acid. |
| Q: What is the molecular weight of nalidixic acid? |
| A: Molecular weight of nalidixic acid is 232.235. |
| Q: How is the water solubility of nalidixic acid? |
| A: Water solubility of nalidixic acid: 0.1 G/L (23 ºC). |
| Q: What is the boiling point of nalidixic acid? |
| A: Boiling point of nalidixic acid is 413.1±45.0 °C at 760 mmHg. |
| Q: What is the InChIKey of nalidixic acid? |
| A: InChIKey of nalidixic acid is MHWLWQUZZRMNGJ-UHFFFAOYSA-N. |
| Q: What is the molecular formula of nalidixic acid? |
| A: Molecular formula of nalidixic acid is C12H12N2O3. |
| Q: What is the melting point of nalidixic acid? |
| A: Melting point of nalidixic acid is 227-229 °C(lit.). |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |
| Henan Tianfu Chemical Co., Ltd. |