(S)-(-)-Nadifloxacin
- Product Name
- (S)-(-)-Nadifloxacin
- CAS No.
- 154357-42-3
- Chemical Name
- (S)-(-)-Nadifloxacin
- Synonyms
- (S)-(-)-OPC-7251;LEVONADIFLOXACIN;(S)-(-)-Nadifloxacin;Nadifloxacin (S)-Isomer;Nadifloxacin Impurity 5;JYJTVFIEFKZWCJ-JTQLQIEISA-N;Nadifloxacin impurities1236;(S)-(-)-Nadifloxacin USP/EP/BP;Nadifloxacin Impurity 5 (S-Nadifloxacin);(4S)-1-Oxo-4β-methyl-5,6-dihydro-7-(4-hydroxypiperidino)-8-fluoro-4H-3a-aza-1H-phenalene-2-carboxylic acid
- CBNumber
- CB71269801
- Molecular Formula
- C19H21FN2O4
- Formula Weight
- 360.38
- MOL File
- 154357-42-3.mol
(S)-(-)-Nadifloxacin Property
- Boiling point:
- 624.9±55.0 °C(Predicted)
- Density
- 1.46
- storage temp.
- Store at -20°C
- solubility
- DMSO : 125 mg/mL (346.86 mM; Need ultrasonic)
- pka
- 5.55±0.40(Predicted)
- form
- Solid
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- N200705
- Product name
- (S)-(-)-Nadifloxacin
- Packaging
- 5mg
- Price
- $250
- Updated
- 2021/12/16
- Product number
- N200705
- Product name
- (S)-(-)-Nadifloxacin
- Packaging
- 10mg
- Price
- $445
- Updated
- 2021/12/16
(S)-(-)-Nadifloxacin Chemical Properties,Usage,Production
Uses
(S)-(-)-Nadifloxacin is an anti-bacterial agent against multidrug-resistant Staphylococcus aureus. Also, it is derived from 6-Fluoro-2-methylquinoline (F595900), which is an quinoline derivative, a highly potent thrombin receptor antagonist.
Definition
ChEBI: (S)-nadifloxacin is a nadifloxacin. It is an enantiomer of a (R)-nadifloxacin.
Biological Activity
Levonadifloxacin is a potent benzoquinolizine fluoroquinolone antibiotic th at is affective against Gram-positive and Gram-negative bacteria, including methicillin- and quinolone-resistant Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae, and Moraxella catarrhalis and atypical pathogens. It appears th at Levonadifloxacin targets staphylococcal DNA gyrase, unlike other quinolones, which primarily inhibit DNA topoisomerase IV.
Synthesis
Starting from 2-bromo-4,5-difluoroacetylaniline, it was reacted with crotonaldehyde under Skraup-Doeber-VonMiller reaction conditions to generate quinoline 2 in 67% yield. Pd-on-carbon catalytic hydrogenation was used to reduce the carbon-bromine bond in 2, and the catalyst was removed by filtration. Platinum-on-carbon was added to the reaction mixture and the hydrogenation conditions were again applied to give tetrahydroquinoline 3 in 97% yield. Tetrahydroquinoline 3 was reacted with 2,3-di-O-benzyl-L-tartaric acid (L-DBTA) and subsequently recrystallized from 60% methanol-water solution to give S-isomer 4 in 35% yield and 100% enantiomeric excess. The recovered R-isomer could be racemized by treatment with methanesulfonic acid. Compound 4 was reacted with diethylethoxymethylvinylmalonate in polyphosphoric acid and subsequently treated with hydrochloric acid to give tricyclic acid 5 in 88% yield. The tricyclic acid 5 chelates with the in situ generated borotriacetate to form the cyclic boronic ester complex 6. The cyclic boronic ester complex 6 is reacted with 4-hydroxypiperidine to afford levonadifloxacin 8 in good yield in a two-step reaction.
Mechanism of action
Levofloxacin is a fluoroquinolone antibiotic that works by inhibiting bacterial DNA gyrase.
Advantages
(S)-(-)-Nadifloxacin is 60-250 times more potent than its R-isomer, nadifloxacin.
(S)-(-)-Nadifloxacin Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from (S)-(-)-Nadifloxacin manufacturers
- Product
- (S)-(-)-Nadifloxacin 154357-42-3
- Price
- US $1.10/g
- Min. Order
- 1g
- Purity
- 99.9%
- Supply Ability
- 100 Tons min
- Release date
- 2021-07-20