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3-Isoxazolecarboxylic acid hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62438-02-2

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62438-02-2 Usage

Function

Antibiotic medication for treating tuberculosis

Mechanism of Action

Inhibits production of mycolic acids in bacterial cell wall

Typical Usage

First-line treatment for tuberculosis, often used in combination with other medications

Side Effects

Potential for liver toxicity and nerve damage

Importance

Critical tool in fighting against tuberculosis, successfully used for decades to treat and prevent spread of disease.

Check Digit Verification of cas no

The CAS Registry Mumber 62438-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,3 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62438-02:
(7*6)+(6*2)+(5*4)+(4*3)+(3*8)+(2*0)+(1*2)=112
112 % 10 = 2
So 62438-02-2 is a valid CAS Registry Number.

62438-02-2Downstream Products

62438-02-2Relevant academic research and scientific papers

Compounds Which Selectively Modulate The CB2 Receptor

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Page/Page column 25, (2011/04/18)

Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.

5,6,7,8-TETRAHYDRO[1,2,4]TRIAZOLO[4,3-a]PYRAZINE DERIVATIVES AS P2X7 MODULATORS

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Page/Page column 106, (2010/11/17)

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein A is hydrogen, C1-4alkyl, C3-6cycloalkyl, C1-3alkoxy, C1-3alkoxy C1-4alkyl, C1-2fluoroalkyl, halogen, NR6 R7, optionally substituted heteroaryl (Het), or optionally substituted phenyl, and R1, R2, R3, R4, R5, R6 and R7 are as defined in the description. The compounds or salts are thought to modulate P2X7 receptor function and to be capable of antagonizing the effects of ATP at the P2X7 receptor. The invention also provides the use of the compound or salt in the treatment or prophylaxis of, for example, inflammatory pain, neuropathic pain, visceral pain, rheumatoid arthritis, osteoarthritis or neurodegenerative disorders.

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