글리세오풀빈

글리세오풀빈
글리세오풀빈 구조식 이미지
카스 번호:
126-07-8
한글명:
글리세오풀빈
동의어(한글):
그레세오풀빈;글리세오풀빈
상품명:
(+)-Griseofulvin
동의어(영문):
GRISEOFULVIN;Griseo;Grisovi;Gris-peg;Fulvicin;Grisactin;Grifulvin V;Grisofulvin;Grysio;Poncyl
CBNumber:
CB1766075
분자식:
C17H17ClO6
포뮬러 무게:
352.77
MOL 파일:
126-07-8.mol
MSDS 파일:
SDS

글리세오풀빈 속성

녹는점
218-220 °C(lit.)
알파
354 º (c=1, dimethylform)
끓는 점
469.04°C (rough estimate)
밀도
1.2579 (rough estimate)
굴절률
1.4429 (estimate)
저장 조건
2-8°C
용해도
물에 거의 녹지 않으며, 디메틸포름아미드와 테트라클로로에탄에 잘 녹고, 무수 에탄올과 메탄올에는 약간 녹습니다.
물리적 상태
가루
색상
흰색~황백색
수용성
실질적으로 불용성
최대 파장(λmax)
321nm(CHCl3)(lit.)
Merck
14,4549
BRN
95226
BCS Class
2 (CLogP), 4 (LogP)
안정성
제공된 대로 구매일로부터 1년 동안 안정적입니다. DMSO, 에탄올 또는 DMF의 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.
InChIKey
DDUHZTYCFQRHIY-RBHXEPJQSA-N
LogP
2.180
CAS 데이터베이스
126-07-8(CAS DataBase Reference)
NIST
Griseofulvin(126-07-8)
IARC
2B (Vol. Sup 7, 79) 2001
EPA
Griseofulvin (126-07-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,Xn
위험 카페고리 넘버 60-61-40-43-45
안전지침서 53-22-36/37/39-45
유엔번호(UN No.) UN 1648 3 / PGII
WGK 독일 3
RTECS 번호 WG9800000
HS 번호 29419090
유해 물질 데이터 126-07-8(Hazardous Substances Data)
독성 LD50 oral in rat: > 10gm/kg
기존화학 물질 KE-05936
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H351 암을 일으킬 것으로 의심됨 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 2 경고 P201, P202, P281, P308+P313, P405,P501
예방조치문구:
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
1
2 0

글리세오풀빈 MSDS


(+)-Griseofulvin

글리세오풀빈 C화학적 특성, 용도, 생산

화학적 성질

Crystalline Solid

용도

It is an antifungal drug. It is used both in animal and in humans, to treat rigworm infections of the skin and nails. It is derived from the mold Penicillium griseofulvum.Environmental contaminants; Food contaminants.

정의

ChEBI: An oxaspiro compound produced by Penicillium griseofulvum. It is used by mouth as an antifungal drug for infections involving the scalp, hair, nails and skin that do not respond to topical treatment.

Indications

Griseofulvin (Fulvicin, Grifulvin V) has been used safely and effectively for decades for dermatophyte infections of scalp and nails and for more widespread skin eruptions. However, infections in certain sites (e.g.. toenails) respond poorly. The drug is generally well tolerated, even in the long-term courses necessary for nail disease.

World Health Organization (WHO)

Griseofulvin, isolated from a penicillin producing mould, has been widely used as a systemically administered antifungal agent in man for over 20 years. It is effective in dermatophyte infections (including tinea barbae and tinea capitis) but it is inactive against yeasts and bacteria. Evidence that very high doses of griseofulvin are carcinogenic, teratogenic and fetotoxic in laboratory animals has led to an acceptance that it should not be used to treat trivial infections that respond to topical therapy. Oral formulations of griseofulvin are included in the WHO Model List of Essential Drugs. (Reference: (WHTAC1) The Use of Essential Drugs, 2nd Report of the WHO Expert Committee, 722, , 1985)

Antimicrobial activity

The spectrum of useful activity is restricted to dermatophytes causing skin, nail and hair infections (Epidermophyton, Microsporum and Trichophyton spp.). Resistance has seldom been reported.

일반 설명

White to pale cream-colored crystalline powder. Odorless or almost odorless. Tasteless. Sublimes without decomposition at 410°F.

공기와 물의 반응

Insoluble in water.

반응 프로필

(+)-Griseofulvin is incompatible with strong oxidizing agents. .

위험도

Possible carcinogen.

화재위험

Flash point data for (+)-Griseofulvin are not available. (+)-Griseofulvin is probably combustible.

Pharmaceutical Applications

A fermentation product of various species of Penicillium, including Pen. griseofulvum. Available as fine-particle or ultrafine- particle formulations for oral use.

Mechanism of action

The mechanism of action of griseofulvin is through binding to the protein tubulin, which interferes with the function of the mitotic spindle and, thereby, inhibits cell division. Griseofulvin also may interfere directly with DNA replication. Griseofulvin is gradually being replaced by newer agents .

Pharmacokinetics

Absorption from the gastrointestinal tract is dependent on drug formulation. Administration with a high-fat meal will increase the rate and extent of absorption, but individuals tend to achieve consistently high or low blood concentrations. It appears in the stratum corneum within 4–8 h as a result of secretion in perspiration. However, levels begin to fall soon after the drug is discontinued, and within 48–72 h it can no longer be detected. It is metabolized in the liver, the metabolites being excreted in the urine. The elimination half-life is 9–21 h.

Clinical Use

Dermatophyte infections of hair, skin and nail

부작용

Adverse reactions occur in about 15% of patients and include headache, nausea, vomiting, rashes and photosensitivity.

신진 대사

Griseofulvin is metabolized by the liver, and its metabolites are excreted in the urine. It is highly protein bound and, therefore, may have high tissue levels. However, tissue levels decrease and fall as soon as griseofulvin is discontinued such that its presence is no longer detectable 2 to 3 days after cessation of therapy.

Purification Methods

Crystallise it from *benzene or EtOH. Purify 2g of griseofulvin by chromatography on Alumina (40 x 1.5cm) and elute with *C6H6/MeOH (199:1) and follow the UV blue fluorescent band. [MacMillan J Chem Soc 1823 1959, Beilstein 18 III/IV 3160, 18/5 V 150.]

글리세오풀빈 준비 용품 및 원자재

원자재

준비 용품


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