옥솔린산

옥솔린산
옥솔린산 구조식 이미지
카스 번호:
14698-29-4
한글명:
옥솔린산
동의어(한글):
옥솔린산
상품명:
Oxolinic acid
동의어(영문):
oxolinic;5-ETHYL-8-OXO-5,8-DIHYDRO-[1,3]DIOXOLO[4,5-G]QUINOLINE-7-CARBOXYLIC ACID;w4565;utibid;ossian;oxoboi;pietil;s-0208;uroxol;starner
CBNumber:
CB8177186
분자식:
C13H11NO5
포뮬러 무게:
261.23
MOL 파일:
14698-29-4.mol
MSDS 파일:
SDS

옥솔린산 속성

녹는점
314-316°C (dec.)
끓는 점
473℃
밀도
1.3038 (rough estimate)
굴절률
1.5500 (estimate)
인화점
>110°(230°F)
저장 조건
2-8°C
용해도
가온과 함께 0.5N NaOH에 용해됨
물리적 상태
결정성 분말
산도 계수 (pKa)
5.94±0.20(Predicted)
색상
하얀색
수용성
3.214mg/L(온도 미표시)
감도
Light Sensitive
Merck
13,7014
BRN
620635
안정성
안정적인. 타기 쉬운.
InChIKey
KYGZCKSPAKDVKC-UHFFFAOYSA-N
CAS 데이터베이스
14698-29-4(CAS DataBase Reference)
EPA
Oxolinic acid (14698-29-4)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn
위험 카페고리 넘버 22
안전지침서 22-24/25-60-36
WGK 독일 3
RTECS 번호 JI5075000
F 고인화성물질 10
HS 번호 29349990
유해 물질 데이터 14698-29-4(Hazardous Substances Data)
독성 LD50 in mice, rats (mg/kg): >6000, >2000 orally (Turner)
기존화학 물질 KE-13605
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:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
1 0

옥솔린산 MSDS


Oxolinic acid

옥솔린산 C화학적 특성, 용도, 생산

개요

Bacterial DNA gyrase is a heterodimeric type II topoisomerase that negatively supercoils circular double-stranded DNA. Oxolinic acid is a quinolone antibiotic that inhibits bacterial DNA gyrase, but not eukaryotic topoisomerases, reversibly binding gyrase subunit A in gyrase-DNA complexes, blocking supercoiling activity and inhibiting DNA synthesis at 0.5-5 μg/ml. Oxolinic acid also blocks neuronal uptake of dopamine in mammals (IC50 = 4.3 μM), leading to an increase in locomotor activity.

화학적 성질

Crystalline Solid

용도

Oxolinic acid is a quinolone antibiotic used for studies on DNA winding and coiling and for studies on dopaminergic neurotransmission processes. It is used to study new transmissible resistance mechanisms qnrA, qnrB, qnrS, and aac(6′)Ib-cr, in Escherichia

정의

ChEBI: A quinolinemonocarboxylic acid having the carboxy group at position 7 as well as oxo and ethyl groups at positions 4 and 1 respectively and a dioxolo ring fused at the 5- and 6-positions. A synthetic antibiotic, it is used in veterinary medicine for the tr atment of bacterial infections in cattle, pigs and poultry.

Antimicrobial activity

Like nalidixic acid, this drug is effective with respect to Gram-negative microorganisms and is used for the same indications. Synonyms of this drug are nidantin, prodoxol, ocolin, uroxol, and others.

일반 설명

Chemical structure: quinolone

Pharmaceutical Applications

An oral 4-quinolone with a tricyclic structure. Its antibacterial spectrum is very similar to that of nalidixic acid, but it is more active againstEnterobacteriaceae (MIC 0.25–2 mg/L). Grampositive bacteria, Ps. aeruginosa and anaerobes are resistant.
After repeated doses of 750 mg twice daily, mean plasma concentrations are initially very low, but steady state is reached at the third day and Cmax is around 3.5 mg/L. Administration with food delays absorption. Binding to plasma protein is about 80%. It undergoes complex biotransformation, and an enterohepatic cycle may account for the increase in the apparent elimination half-life from 4 to 15 h over 7 days of treatment as well as for the 20% of dose which can be recovered from the feces. About 50% of the dose appears in the urine in the first 24 h, partly in the form of metabolites, some of which display antibacterial activity.
Side effects common to the quinolones occur frequently. About one-quarter of patients treated with 750 mg every 12 h suffer nausea and vomiting or restlessness and insomnia. Its only use is in the treatment of lower urinary tract infections.

Safety Profile

Moderately toxic by ingestion. Low toxicity by skin contact. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Purify the acid by recrystallisation from aqueous Me2CO, 95% EtOH or dimethylformamide. It has UV 220, (255.5sh), max 259.5, 268, (298sh, 311sh), 321 and 326nm [ 14.8, (36.8sh), 38.4, 38.4, (6.4sh, 9.2sh), 10.8 and 11.2 x 103]. [Kaminsky & Mettzer J Med Chem 11 160 1968, Beilstein 17 H 6, 17 I 3, 17 II 202, 17 III/IV 13, 17/1 V 11.]

옥솔린산 준비 용품 및 원자재

원자재

준비 용품


옥솔린산 공급 업체

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