C1761
分支酸 来源于产气肠杆菌
≥80%
别名:
反式-3-([1-羧基乙烯基]氧)-4-羟基-1,5-环己二烯-1-羧酸
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关于此项目
经验公式（希尔记法）:
C10H10O6
化学文摘社编号:
分子量:
226.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥80%
Form:
powder
Quality Level
assay
≥80%
form
powder
shipped in
dry ice
storage temp.
−20°C
SMILES string
O[C@@H]1C=CC(=C[C@H]1OC(=C)C(O)=O)C(O)=O
InChI
1S/C10H10O6/c1-5(9(12)13)16-8-4-6(10(14)15)2-3-7(8)11/h2-4,7-8,11H,1H2,(H,12,13)(H,14,15)/t7-,8-/m1/s1
InChI key
WTFXTQVDAKGDEY-HTQZYQBOSA-N
Application
分支酸是一种代谢物，通常用于研究分支酸-预苯酯重排和合成分支酸衍生物。
通过莽草酸途径生物合成芳香氨基酸的中间体。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Expanding the genetic code.
Wang, Lei and Schultz, Peter G
Angewandte Chemie (International Edition in English), 44(1), 34-66 (2005)
Gamma Chi et al.
Biochemistry, 51(24), 4868-4879 (2012-05-23)
MbtI is the salicylate synthase that catalyzes the first committed step in the synthesis of the iron chelating compound mycobactin in Mycobacterium tuberculosis. We previously developed a series of aromatic inhibitors against MbtI based on the reaction intermediate for this
Nivedita Nagachar et al.
FEMS microbiology letters, 308(2), 159-165 (2010-05-22)
Mycobacterium smegmatis acquires extracellular iron using exochelin, mycobactin and carboxymycobactin. The latter two siderophores are synthesized from salicylic acid, which, in turn, is derived from chorismic acid in the shikimic acid pathway. To understand the conversion mechanism of chorismic acid
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| C1761-25MG | 04061832621128 |
| C1761-5MG | 04061832621135 |
| C1761-100MG | 04061832621104 |
| C1761-10MG | 04061832621111 |