MECLOFENAMATE SODIUM

MECLOFENAMATE SODIUM 구조식 이미지
카스 번호:
6385-02-0
상품명:
MECLOFENAMATE SODIUM
동의어(영문):
ci583;C02996;Movens;meclomen;Meclonax;Meclofenamate;sodiummeclophenamate;SODIUM MECLOFENAMATE;MECLOFENAMATE SODIUM;MECLOFENAMATESODIUM,USP
CBNumber:
CB7102365
분자식:
C14H10Cl2NO2.Na
포뮬러 무게:
318.13
MOL 파일:
6385-02-0.mol
MSDS 파일:
SDS

MECLOFENAMATE SODIUM 속성

녹는점
287-291 °C
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
백색 고체.
색상
흰색에서 황백색까지
수용성
50mg/ml로 물에 용해됩니다. DMF, DMSO 또는 에탄올에도 용해됩니다.
Merck
14,5779
안정성
흡습성
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
WGK 독일 3
RTECS 번호 CB2975500
HS 번호 2922498050
기존화학 물질 KE-10153
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
0
3 0

MECLOFENAMATE SODIUM C화학적 특성, 용도, 생산

개요

Meclofenamate is a time-dependent, non-specific competitive inhibitor of COX-1 and -2. The IC50 values for inhibition of human recombinant COX-1 and -2 are 1.5 and 9.7 μM, respectively for instantaneous inhibition. However, the IC50 is much lower if pre-incubated with the enzyme.

용도

Meclofenamate Sodium is an NSAID used in the treatment of chronic pain.

정의

ChEBI: An organic sodium salt derived from meclofenamic acid. Its monohydrate is used for the treatment of dysmenorrhoea (painful periods), osteoarthritis and rheumatoid arthritis.

Indications

Meclofenamate sodium (Meclomen) is prescribed for rheumatoid arthritis and osteoarthritis. The fenamates show no clear superiority in antiinflammatory activity and may produce more adverse effects than other NSAIDs.

일반 설명

Meclofenamate sodium (Meclomen) is available for use inthe treatment of acute and chronic RA, OA, and primarydysmenorrhea. It is metabolized in a similar manner tomefenamic acid discussed above, thus a similar restriction isalso applied to meclofenamate. The most significant side effectsare GI, including diarrhea.

Pharmacokinetics

Meclofenamate sodium is rapidly and almost completely absorbed following oral administration, reaching peak plasma levels within 2 hours. It is highly bound to plasma proteins (99%) and has a plasma half-life of 2 to 4 hours. Metabolism involves oxidation of the methyl group, aromatic hydroxylation, monodehalogenation, and conjugation. Urinary excretion accounts for approximately 75% of the administered dose. The major metabolite is the product of 3′-methyl oxidation and has been shown to possess anti-inflammatory activity.
Metabolism of meclofenamic acid..jpg

Clinical Use

Meclofenamate sodium is indicated for the relief of mild to moderate pain, the acute and chronic treatment of rheumatoid arthritis and osteoarthritis, the treatment of primary dysmenorrhea, and the treatment of idiopathic, heavy menstrual blood loss.

MECLOFENAMATE SODIUM 준비 용품 및 원자재

원자재

준비 용품


MECLOFENAMATE SODIUM 공급 업체

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LEAPCHEM CO., LTD.
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Aladdin Scientific
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sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
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sales@amadischem.com China 131980 58

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