시틴딘

시틴딘
시틴딘 구조식 이미지
카스 번호:
65-46-3
한글명:
시틴딘
동의어(한글):
시틴딘;사이티딘
상품명:
Cytidine
동의어(영문):
4-aMino-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)pyriMidin-2(1H)-one;Cyd;Citydine;Cytosine β-D-riboside;Cytosine β-D-riboside;Citidine;Cytidin;Cytidine;Cytinide;Cytidylic
CBNumber:
CB7854079
분자식:
C9H13N3O5
포뮬러 무게:
243.22
MOL 파일:
65-46-3.mol
MSDS 파일:
SDS

시틴딘 속성

녹는점
210-220 °C (dec.) (lit.)
끓는 점
386.09°C (rough estimate)
알파
31.5 º (c=0.6, H2O 25 ºC)
밀도
1.3686 (rough estimate)
굴절률
34 ° (C=0.7, H2O)
저장 조건
2-8°C
용해도
H2O: 50 mg/mL
산도 계수 (pKa)
4.22, 12.5(at 25℃)
물리적 상태
가루
색상
흰색에서 거의 흰색
optical activity
[α]20/D +33°, c = 2 in H2O
수용성
녹는
감도
Hygroscopic
Merck
14,2786
BRN
89173
안정성
안정적인. 강한 산화제와 호환되지 않습니다. 습기로부터 보호하십시오.
LogP
-1.808 (est)
CAS 데이터베이스
65-46-3(CAS DataBase Reference)
NIST
Cytidine(65-46-3)
EPA
Cytidine (65-46-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험 카페고리 넘버 68
안전지침서 24/25
WGK 독일 3
RTECS 번호 UW7370000
F 고인화성물질 10-23
TSCA Yes
HS 번호 29349990
독성 LD50 intraperitoneal in mouse: 2700mg/kg
기존화학 물질 KE-01588
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
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
0 1

시틴딘 MSDS


Cytidine

시틴딘 C화학적 특성, 용도, 생산

개요

Cytidine is a pyrimidine nucleoside that is composed of the pyrimidine base cytosine attached to the sugar ribose. As a constituent of RNA, cytidine pairs with guanine, and it is a precursor of uridine. Cytidine can incur several modifications in mRNA, including methylation and acetylation, that function to regulate translation. Cytidine can also be formylated to 5-formylcytidine in mitochondrial methionine transfer RNA (tRNAMet).

화학적 성질

Cytidine is a component of RNA. It is a white water-soluble solid. which is only slightly soluble in ethanol.There are a variety of cytidine analogs with potentially useful pharmacology.

용도

Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA. It was isolated from yeast nucleic acid. It can increases cell membrane phospholipids. Cytidine is used to synthesize enzyme inhibitors, antiviral agents, and anticancer agents. And also used as constituent of nucleic acids.

주요 응용

Cytidine has been used as a non-essential aminoacid component of minimal essential medium (MEM) to analyse interspecies somatic cell nucleus transfer (iSCNT)-derived blastocysts. It has also been used as a supplement in the culture medium of HeLa cells, to study the effects of cytidine addition on rods and rings (RR) induced by glutamine deprivation.
Cytidine has been used as a component to prepare ribonucleoside stock solution to assess its effects on the anaerobic growth of several Bacillus mojavensis strains.

정의

ChEBI: cytidine is a pyrimidine nucleoside in which cytosine is attached to ribofuranose via a beta-N(1)-glycosidic bond. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It derives from a cytosine.The derivednucleotides, cytidine mono-, di-, andtriphosphate (CMP, CDP, and CTP respectively)participate in various biochemicalreactions, notably inphospholipid synthesis.

일반 설명

White crystalline powder.

공기와 물의 반응

Cytidine is hygroscopic. Water soluble.

반응 프로필

Cytidine is incompatible with strong oxidizing agents. . Will react as a weak base.

화재위험

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

Purification Methods

Cytidine crystallises from 90% aqueous EtOH. It has also been converted to sulfate by dissolving (~200mg) in a solution of EtOH (10mL) containing H2SO4 (50mg), whereby the salt crystallises out. It is collected, washed with EtOH and dried for 5hours at 120o/0.1mm. The sulfate has m 225o. The free base is obtained by shaking the salt solution with a weak ion-exchange resin, filtering, evaporating and recrystallising the residue from EtOH as before. [Fox & Goodman J Am Chem Soc 73 3256 1956, Fox & Shugar Biochim Biophys Acta 9 369 1952; see Prytsas & Sorm in Synthetic Procedures in Nucleic Acid Chemistry (Zorbach & Tipson Eds) Vol 1 404 1973.] [Beilstein 25 III/IV 3667.]

시틴딘 준비 용품 및 원자재

원자재

준비 용품


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