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ChemicalBook >> CAS DataBase List >> Ftivazide

Ftivazide

Ftivazide price.
  • $110 - $605
  • Product name: Ftivazide
  • CAS: 149-17-7
  • MF: C14H13N3O3
  • MW: 271.27
  • EINECS:
  • MDL Number:MFCD00033812
  • Synonyms:Ftivazide;phthivazid;4-pyridinecarboxylic acid, ((4-hydroxy-3-methoxyphenyl)methylene)hydrazide;ftivazid;Isonicotinic acid vanillylidenehydrazide;isonicotinic acid, vanillylidenehydrazide;phtivazid;vanicid
2 prices
Selected condition:
Brand
  • Sigma-Aldrich
  • TRC
Package
  • 50mg
  • 500mg
  • ManufacturerSigma-Aldrich
  • Product numberS730971
  • Product descriptionISONICOTINIC 4-HYDROXY-3-METHOXYBENZYLIDENEHYDRAZIDE Aldrich
  • Packaging50mg
  • Price$110
  • Updated2024-03-01
  • Buy
  • ManufacturerTRC
  • Product numberI821765
  • Product descriptionIsonicotinicAcidVanillylidenehydrazide
  • Packaging500mg
  • Price$605
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich S730971 ISONICOTINIC 4-HYDROXY-3-METHOXYBENZYLIDENEHYDRAZIDE Aldrich 50mg $110 2024-03-01 Buy
TRC I821765 IsonicotinicAcidVanillylidenehydrazide 500mg $605 2021-12-16 Buy

Properties

Melting point :219-220 °C
Boiling point :414.36°C (rough estimate)
Density :1.2122 (rough estimate)
refractive index :1.5700 (estimate)
pka :8.65±0.35(Predicted)

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

Isonicotinic Acid Vanillylidenehydrazide exhibits anti-mycobacterial activity against Mycobacterium tuberculosis and anti-microbial activity against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Candida albicans, and Aspergillus niger.Also, it is derived from Isoniazid (I821450), which is an antibiotic for treatment of Mycobacterium tuberculosis, inhibits mycolic acid biosynthesis. Metabolized by hepatic N-acetyltransferase (NAT) and cytochrome P450 2E1 (CYP2E1) to form hepatotoxins. Selectively induces expression of CYP2E1. Reversibly inhibits CYP2C19 and CYP3A4 activities, and mechanistically inactivates CYP1A2, CYP2A6, CYP2C19 and CYP3A4 at clinically relevant concentrations. Antibacterial (tuberculostatic).

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