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CasNo: 1075240-43-5
Omadacycline Tosylate 1075240-43-5 with purity >99% Low price in stock We supply high quality OMadacycline (tosylate) (CAS 1075240-43-5), in stock, factory directly supply to clients, lower prices, more competitiveness.
OMadacycline (tosylate) is , while it's Molecular Formula is C7H8O3S*C29H40N4O7. Used in Pharmaceutical Industry:
OMadacycline (tosylate) is used as an antibiotic for treating a wide range of bacterial infections due to its broad-spectrum activity and effectiveness against both Gram-positive and Gram-negative organisms.
Used in Combating Antibiotic Resistance:
OMadacycline (tosylate) is utilized as a tool in the fight against antibiotic resistance, given its efficacy against drug-resistant strains of bacteria, which is crucial in managing and preventing the spread of resistant infections.
Used in Patient Care:
OMadacycline (tosylate) is employed as a therapeutic option for patients with various infections, offering a valuable choice due to its well-tolerated nature and favorable safety profile, ensuring patient comfort and compliance during treatment.
The CAS number of OMadacycline (tosylate) is 1075240-43-5.
More information of OMadacycline (tosylate) 1075240-43-5 are:
CAS Number |
1075240-43-5 |
Molecular Formula |
C7H8O3S*C29H40N4O7 |
Molecular Weight |
728.864 |
OMadacycline (tosylate) is a novel tetracycline antibiotic characterized by its broad-spectrum activity against various bacterial infections. It functions by inhibiting protein synthesis in bacterial cells, which results in their death. OMadacycline (tosylate) is notable for its effectiveness against both Gram-positive and Gram-negative bacteria, as well as its activity against drug-resistant strains, positioning it as a significant asset in combating antibiotic resistance. Additionally, OMadacycline (tosylate) is recognized for its favorable safety profile and good tolerability, making it a valuable treatment option for patients with diverse infections.
Articles related to OMadacycline (tosylate):
Article |
Source |
Synthesis development of an aminomethylcycline antibiotic via an electronically tuned acyliminium Friedel-Crafts reaction |
Chung, John Y.L.,Hartner, Frederick W.,Cvetovich, Raymond J. body text, p. 6095 - 6100 (2009/04/05) |
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