As a leading 1-Cyclopropyl-8-(Difluoromethoxy)-7-[(1R)-1-Methyl-2,3-Dihydro-1H-Isoindol-5-Yl]-4-Oxo-1,4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
This product 1-Cyclopropyl-8- (Difluoromethoxy) -7- [ (1R) -1-Methyl-2,3-Dihydro-1H-Isoindol-5-Yl] -4-Oxo-1, 4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1) What is the chemical structure
This is the chemical structure analysis of 1-cyclopropyl-8- (difluoromethoxy) -7- [ (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl] -4-oxo-1,4-dihydroquinoline-3-carboxylic acid methanesulfonate monohydrate (1:1:1).
Looking at its name, it can be seen that the core structure of this compound is a quinoline ring. In the first position of the quinoline ring, there is a cyclopropyl group, which has a stable structure and affects the steric hindrance and electron cloud distribution of the compound. The difluoromethoxy group attached to the eighth position has strong electronegativity, which can change the lipophilicity and metabolic stability of the compound. In the seventh position [ (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl], the isoindole structure endows the compound with specific biological activity and recognition ability, and the 1-methyl makes the stereochemistry of the structure more complicated. Carbonyl at the fourth position affects the electron cloud conjugation of the compound, which is related to its chemical reactivity. 3-Position carboxylic acid, acidic, can participate in the salt-forming reaction, form methanesulfonic acid with methanesulfonic acid, and improve the solubility of the compound. There is also a monohydrate, where water molecules bind to the compound or affect its physical properties, such as melting point, stability, etc.
The chemical structure of this compound, the interaction of various parts, jointly determines its physical, chemical and biological activities and many other properties.
What is the main use of 1-Cyclopropyl-8- (Difluoromethoxy) -7- [ (1R) -1-Methyl-2, 3-Dihydro-1H-Isoindol-5-Yl] -4-Oxo-1, 4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1)
1-Cyclopropyl-8- (difluoromethoxy) -7- [ (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl] -4-oxo-1,4-dihydroquinoline-3-carboxylic acid methanesulfonate monohydrate (1:1:1), this is a single medicine stone, its use is quite critical.
This medicine is often used in the field of antibacterial in the treatment of diseases. Because it has a unique chemical structure, it can interfere with the specific physiological process of bacteria, thereby inhibiting the growth and reproduction of bacteria. For example, in some infectious diseases, bacteria breed wantonly, endangering human health. And this medicine stone can precisely act on bacteria by virtue of its characteristics, like a sharp blade breaking bamboo, making the life activities of bacteria unsustainable.
In medical practice, it can deal with infections caused by various bacteria, such as respiratory tract infections, common cough, fever and other symptoms, or caused by bacteria. This medicine has the opportunity to show its skills and help patients relieve pain. Or urinary system infections, patients with frequent urination, urgency, urinary pain and other discomforts are also expected to be improved by it.
Furthermore, this medicine stone may also be effective when preventing infection during surgery. Before or after surgery, in order to prevent bacteria from invading the wound and causing infection, the rational use of this medicine can protect the barrier, reduce the risk of infection, and help patients recover smoothly.
What is the market outlook for this product 1-Cyclopropyl-8- (Difluoromethoxy) -7- [ (1R) -1-Methyl-2,3-Dihydro-1H-Isoindol-5-Yl] -4-Oxo-1, 4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1)
There are currently drugs 1 - Cyclopropyl - 8 - (Difluoromethoxy) - 7 - [ (1R) - 1 - Methyl - 2,3 - Dihydro - 1H - Isoindol - 5 - Yl] - 4 - Oxo - 1,4 - Dihydroquinoline - 3 - Carboxylic Acid Methanesulfonate Hydrate (1:1:1). The market prospect of this drug is related to many parties.
The market of Guanfu medicine is changing, the spectrum of diseases is changing, and the demand is changing. In the field of antibacterial drugs, drug-resistant bacteria are thriving, and there is a strong demand for efficient and specific antibacterial agents. If this drug has excellent antibacterial activity and is effective against drug-resistant strains, it will definitely be able to take advantage of the situation and enter the market and be favored.
Furthermore, the process of research and development requires both cost and progress. If the research and development goes well, the cost is controllable, and it can be quickly pushed to the market to seize the opportunity, the prospect is promising. On the contrary, the research and development is blocked, the time is delayed, the cost increases sharply, and the benefits of the market may be lost.
The orientation of the policy is also the key. The pharmaceutical policy strictly controls quality, pricing and access. If this drug complies with the policy norms, it will be approved and supported, and the sales will be smooth. If it violates the policy, it will be difficult for a good drug to be delivered in the world.
The competition situation cannot be ignored There are many similar drugs, and each has its own capabilities. This drug needs to have unique advantages, such as superior efficacy, minimal side effects, and ease of administration, in order to stand out from the competition.
In summary, the market prospects of this drug depend on its antibacterial efficacy, research and development process, policy fit, and competitive response. With advantages, the future is bright, otherwise it may be in trouble.
What is the safety of 1-Cyclopropyl-8- (Difluoromethoxy) -7- [ (1R) -1-Methyl-2, 3-Dihydro-1H-Isoindol-5-Yl] -4-Oxo-1, 4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1)
This is a substance named 1-cyclopropyl-8- (difluoromethoxy) -7- [ (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl] -4-oxo-1,4-dihydroquinoline-3-carboxylic acid methanesulfonate monohydrate (1:1:1). In terms of its safety, it needs to be examined from various angles.
In terms of chemical structure, the existence of groups such as cyclopropyl and difluoromethoxy gives them specific chemical activities. However, these groups react in different environments or with other substances, and the safety of their products should not be ignored. In the field of drug development, compounds with similar structures may have adverse reactions such as allergies and organ damage in animal experiments. For example, there have been drugs containing similar fluorinated groups that have affected the metabolic function of the liver in animal experiments.
Looking at the morphology of methanesulfonate and hydrate, the introduction of methanesulfonate groups will affect the solubility and stability of the substance. During storage, if the ambient humidity and temperature are improper, or deliquescence or decomposition occurs, the safety of the hydrate will be affected. If the number of crystal waters of the hydrate changes, it may also lead to changes in the crystal form, affecting its pharmacological activity and safety. In the past, there have been drugs with significant changes in bioavailability due to changes in crystal form, causing serious side effects.
From a toxicological perspective, the acute toxicity, chronic toxicity, and genetic toxicity of this compound need to be studied in depth. Although detailed toxicological data on this specific substance has not been retrieved yet, some similar structural drugs, after long-term administration, will cause damage to the reproductive system and immune system of experimental animals.
In summary, the safety of this substance requires rigorous experiments and studies, and comprehensive assessments from chemical properties, stability, toxicology, etc. can be determined. It must not be made rashly.
1-Cyclopropyl-8- (Difluoromethoxy) -7- [ (1R) -1-Methyl-2, 3-Dihydro-1H-Isoindol-5-Yl] -4-Oxo-1, 4-Dihydroquinoline-3-Carboxylic Acid Methanesulfonate Hydrate (1:1:1) What are the advantages compared to other congeneric products
1-Cyclopropyl-8- (difluoromethoxy) -7- [ (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl] -4-oxo-1,4-dihydroquinoline-3-carboxylic acid methanesulfonate monohydrate (1:1:1) Compared with other congeneric products, its advantages lie in many aspects.
This compound has a unique structure, and groups such as cyclopropyl and difluoromethoxy give it specific physicochemical properties. From the perspective of pharmacological activity, or due to its delicate structure, it has high affinity and selectivity for specific targets, and can act precisely, with better curative effect and lower side effects. As the ancient law said, "Those who are unique must have the ability to be different from those who are normal." The unique structure makes it possible to open up new paths in the mechanism of action, just like a unique weapon to defeat the enemy.
Furthermore, its methanesulfonate monohydrate form may improve the solubility and stability of the original drug. In the preparation and storage of drugs, good solubility is conducive to the development of preparations, and good stability can ensure the long-lasting effect of the drug, just as the ancient books say "only when the foundation is stable can it last for a long time." In the preparation process, good properties facilitate the preparation of different dosage forms to meet diverse clinical needs.
At the same time, its chiral centers such as (1R) -1-methyl-2,3-dihydro-1H-isoindole-5-yl have a significant impact on activity, and a single chiral configuration may make it more closely bound to the target and enhance pharmacological activity.