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  • CAS:479050-91-4|N-3-氧-十六烷基-11Z-烯酰基-L-高丝氨酸内酯

CAS:479050-91-4|N-3-氧-十六烷基-11Z-烯酰基-L-高丝氨酸内酯

  • 产品别名:

    N-3-oxo-hexadec-11Z-enoyl-L-Homoserine lactone

  • CAS   号:

    479050-91-4

  • 分  子 量:

    351.5

  • 分  子 式:

    C₂₀H₃₃NO₄

  • 产品纯度:

    ≥95%

  • 产品规格:

    100mg,500mg(可根据需求定制)

  • 运输条件:

    顺丰速运包邮

  • 产品说明:

    此产品仅用于科研,不能用于人体治疗、药物开发、和其他商业用途。

  • 更新时间:

    2023-04-13 10:21:16

产品名称:N-3-氧-十六烷基-11Z-烯酰基-L-高丝氨酸内酯
英文名称:N-3-oxo-hexadec-11Z-enoyl-L-Homoserine lactone
英文别名:3-oxo-C16:1-Δ11cis-(L)-HSL; 3- oxo- N- [(3S)- tetrahydro- 2- oxo- 3- furanyl]- (11Z)- hexadecenamide
规格或纯度:A solution in acetonitrile
运输条件:超低温冰袋运输
N-3-氧代十六烷基-11Z-烯酰基-L-高丝氨酸内酯也被称为3-氧代-C | 16 |:1-Δ| 11 |顺式(L)-HSL。N-酰化的高丝氨酸内酯(AHL)包括一类自诱导剂,每一种通常都由与高丝氨酸内酯偶联的脂肪酸组成。调节细菌群体感应信号系统以抑制发病机理代表了一种用于治疗感染性疾病的抗菌疗法的新方法。AHL的酰基长度(C | 4 | -C | 18 |),C3的取代(氢,羟基或氧代基)以及在存在或不存在一个或多个碳-碳双键的情况下都不同脂肪酸链。这些差异通过LuxR家族的转录调节子的亲和力赋予信号
N-3-oxo-hexadec-11Z-enoyl-L-Homoserine lactone is also known as 3-oxo-C|16|:1-Δ|11|cis-(L)-HSL. The N-acylated homoserine lactones (AHLs) comprise one class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone. Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases. AHLs vary in acyl group length (C|4|-C|18|), in the substitution of C3 (hydrogen, hydroxyl, or oxo group), and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family. An unspecified positional and geometric isomer of 3-oxo-C|16|:1-(L)-HSL is produced by the F2/5 strain of A. vitis, the bacterium responsible for grape crown gall and its resulting loss of agricultural productivity.
CAS编号:479050-91-4
折光率:n20D~1.49
沸点:84° C
溶解性:Soluble in DMSO (~30 mg/ml), DMF (~30 mg/ml), ethanol, and primary alcohols.
储存温度-20°C储存
分子量:351.5
分子式:C₂₀H₃₃NO₄
Smiles:CCCCCCC=CCCCCCC(=O)CC(=O)NC1CCOC1=O
PubChem CID:53394019
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