빈크리스틴 황산염

빈크리스틴 황산염
빈크리스틴 황산염 구조식 이미지
카스 번호:
2068-78-2
한글명:
빈크리스틴 황산염
동의어(한글):
빈크리스틴황산염;빈크리스틴황산염(VINCRISTINESULFATE)
상품명:
Vincristine sulfate
동의어(영문):
oncovin;VCR;NovopharM;VINCRISTINE SULPHATE;LEUROCRISTINE SULFATE;VINCRISTINE SULFATE USP;VINCRISTINE SULFATE SALT;onkovin;nsc67574;Vincrisul
CBNumber:
CB9479083
분자식:
C46H58N4O14S
포뮬러 무게:
923.04
MOL 파일:
2068-78-2.mol
MSDS 파일:
SDS

빈크리스틴 황산염 속성

녹는점
300 °C
끓는 점
273-281 °C
알파
D26 +8.5° (c = 0.8)
저장 조건
Sealed in dry,Store in freezer, under -20°C
용해도
메탄올: 용해성20mg/mL
물리적 상태
동결건조된 분말
색상
흰색에서 황백색까지
수용성
24 ºC에서 >=1g/100mL
BRN
3924631
안정성
제공된 대로 구매일로부터 2년 동안 안정적입니다. 증류수 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.
InChIKey
AQTQHPDCURKLKT-HSMPTBRCNA-N
IARC
3 (Vol. 26, Sup 7) 1987
EPA
Vincristine sulfate (2068-78-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T
위험 카페고리 넘버 61-36/37/38-63-23/24/25-68-62-25
안전지침서 22-24/25-53-45-37/39-26-36/37/39-36/37
유엔번호(UN No.) UN 2811 6.1/PG 2
WGK 독일 3
RTECS 번호 OH6340000
F 고인화성물질 8-10
위험 등급 6.1(a)
포장분류 II
HS 번호 29399990
독성 LD50 intraperitoneal in mouse: 3mg/kg
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
H300 삼키면 치명적임 급성 독성 물질 - 경구 구분 1,2 위험 GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
H341 유전적인 결함을 일으킬 것으로 의심됨 (노출되어도 생식세포 유전독성을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 생식세포 변이원성 물질 구분 2 경고 P201,P202, P281, P308+P313, P405,P501
예방조치문구:
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P405 밀봉하여 저장하시오.
NFPA 704
0
4 0

빈크리스틴 황산염 MSDS


Leurocristine sulfate salt

빈크리스틴 황산염 C화학적 특성, 용도, 생산

화학적 성질

Crystalline Solid

용도

Vincristine sulfate, is used as an anticancer agent, microtubule disrupter, Induces apoptosis in human lymphoma cells. Other applications include as a cell cycle arresting, apoptotic inducing alkaloid.

일반 설명

Vincristine sulfate appears as an anticancer drug. White to slightly yellow, amorphous or crystalline powder. Sensitive to light. Odorless. pH (0.1% solution) 3.5 - 4.5. (NTP, 1992)

공기와 물의 반응

Very hygroscopic. Water soluble.

반응 프로필

Sensitive to hydrolysis, oxidation and heat. Incompatible with strong oxidizing agents. .

화재위험

Flash point data for Vincristine sulfate are not available; however, Vincristine sulfate is probably combustible.

생물학적 활성

Anticancer agent; microtubule disrupter. Induces apoptosis in human lymphoma cells.

Clinical Use

Vincristine sulfate is available as a 1-mg/mL solution in 1-,2-, and 5-mL vials for IV administration in acute leukemiaand as part of a multidrug regime for Hodgkin’s and neuroblastoma, Ewing sarcoma, Wilms tumor, soft tissuesarcoma, testicular cancer, liver cancer, and head and neckcancers. It has also been utilized in treating pediatric cancer.

신진 대사

Vincristine is metabolised in the liver by the cytochrome P450 isoenzymes CYP3A4 and CYP3A5 and excreted mainly in the bile; about 70-80 % of a dose is found in faeces, as unchanged drug and metabolites (40-50 %), while 10-20 % appears in the urine.
Vincristine is highly protein bound (75%) and may also bindto platelets that contain large amounts of tubulin. Numerousmetabolites have been detected and several have been identified,one of which is the 4-O-desacetyl derivative. The metabolismthat does occur is believed to largely be mediatedby CYP3A. Elimination occurs primarily in the bile with aterminal elimination half-life of 23 to 85 hours.

Purification Methods

The salt is recrystallised from MeOH. It has UV max at 220, 255 and 296nm (log  4.65, 4.21 and 4.18). It is a monoamine oxidase inhibitor and is used in cancer research [Son et al. J Med Chem 33 1845 1990, Horio et al. Proc Natl Acad Sci USA 85 3580 1988].

Mode of action

Vincristine Sulfate is the sulfate salt of a natural alkaloid isolated from the plant Catharanthus roseus (Vinca rosea L.) with antimitotic and antineoplastic activities. Vincristine binds irreversibly to microtubules and spindle proteins in S phase of the cell cycle and interferes with the formation of the mitotic spindle, thereby arresting tumor cells in metaphase. This agent also depolymerizes microtubules and may also interfere with amino acid, cyclic AMP, and glutathione metabolism; calmodulin-dependent Ca(2+)-activated ATPase activity; cellular respiration; and nucleic acid and lipid biosynthesis.

Toxicity evaluation

The mostcommonly seen toxicity for vincristine is a dose-limitingneurotoxicity caused by effects on axonal microtubules.Symptoms are variable and include peripheral neuropathy,ataxia, seizure, bone pain, and coma. Constipation is also acommonly seen toxicity, and laxatives may be used prophylactically.Other toxicities include alopecia, skin rash, mildmyelosuppression, secretion of antidiuretic hormone,azospermia, and amenorrhea.

빈크리스틴 황산염 준비 용품 및 원자재

원자재

준비 용품


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