페니실린산

페니실린산
페니실린산 구조식 이미지
카스 번호:
90-65-3
한글명:
페니실린산
동의어(한글):
페니실린산
상품명:
PENICILLIC ACID
동의어(영문):
NSC 402844;pencillicacid;PENICILLINACID;PENICILLIC ACID;kyselinapenicilova;PENICILLIC ACID 99%;Penicillic acid,99%;Penicillic acid, 99% 25MG;Benzylpenicillin Impurity 26;3-methoxy-5-methyl-4-oxo-5-hexadienoicacid
CBNumber:
CB0338325
분자식:
C8H10O4
포뮬러 무게:
170.16
MOL 파일:
90-65-3.mol
MSDS 파일:
SDS

페니실린산 속성

녹는점
83-87 °C
끓는 점
219.79°C (rough estimate)
밀도
1.1456 (rough estimate)
굴절률
1.4425 (estimate)
저장 조건
Store at 2-8
용해도
DMSO: >10mg/mL
산도 계수 (pKa)
3.90±0.33(Predicted)
물리적 상태
고체
물리적 상태
단단한 모양
색상
석유 에테르에서 바늘 같은 물질의 형성
Merck
13,7163
CAS 데이터베이스
90-65-3
IARC
3 (Vol. 10, Sup 7) 1987
EPA
Penicillic acid (90-65-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,T
위험 카페고리 넘버 36/37/38-20/21/22-22
안전지침서 37/39-26-24/25
유엔번호(UN No.) 2811
RTECS 번호 MM2625000
위험 등급 6.1(b)
포장분류 III
HS 번호 29189900
유해 물질 데이터 90-65-3(Hazardous Substances Data)
독성 LD50 i.p. in mice: 90.00 mg/kg (Chan et al.)
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:
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
NFPA 704
0
1 0

페니실린산 C화학적 특성, 용도, 생산

개요

Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes. It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.

화학적 성질

white to light beige crystals or powder

용도

Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes. It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.

Safety Profile

Poison by intravenous, subcutaneous, and intraperitoneal routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Questionable carcinogen with experimental neoplastigenic data. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

The lactone (furanone, anhydrous) hydrolyses to the acid (3-methoxy-4-oxo-hexa-2,5-dienoic acid, hydrate). It crystallises from water as the monohydrate (acid), or from pet ether as the anhydrous (lactone) compound. The free acid is in equilibrium with the lactone. UV: max 221nm ( 12,500) in 0.02M KOH; 228nm ( 11,500) in 0.02M HCl [Raphael J Chem Soc 1508 1948]. [Beilstein 3 II 519, 3 III 1467.] It is a possible antineoplastic.

페니실린산 준비 용품 및 원자재

원자재

준비 용품


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