所有图片(1)
About This Item
线性分子式:
HOC6H3(NH2)CO2H
CAS号:
分子量:
153.14
Beilstein:
2803663
MDL编号:
UNSPSC代码:
12352106
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
98%
形式
solid
反应适用性
reaction type: solution phase peptide synthesis
mp
247 °C (dec.) (lit.)
应用
peptide synthesis
SMILES字符串
Nc1ccc(O)cc1C(O)=O
InChI
1S/C7H7NO3/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3,9H,8H2,(H,10,11)
InChI key
HYNQTSZBTIOFKH-UHFFFAOYSA-N
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相关类别
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
V K Velikov et al.
Terapevticheskii arkhiv, 63(10), 44-49 (1991-01-01)
Hemocoagulation was examined in 477 diabetes mellitus patients. Whatever the disease type, severity, duration and the intensity of microvascular complications, diabetes mellitus was discovered to be marked by the development of chronic intravascular blood microcoagulation associated with primary hyperactivation of
[Diabeton in the treatment of stage I nephroangiopathy in insulin-dependent diabetes mellitus].
E P Kashirina et al.
Sovetskaia meditsina, (1)(1), 68-69 (1991-01-01)
Deze Kong et al.
Science advances, 6(44) (2020-11-01)
Chalcone synthase (CHS) canonically catalyzes carbon-carbon bond formation through iterative decarboxylative Claisen condensation. Here, we characterize a previously unidentified biosynthetic capability of SlCHS to catalyze nitrogen-carbon bond formation, leading to the production of a hydroxycinnamic acid amide (HCAA) compound. By
T A Buĭdina et al.
Sovetskaia meditsina, (7)(7), 14-16 (1991-01-01)
Newly detected noninsulin--dependent diabetes mellitus is shown to have changes in phospholipid structure of erythrocytic membranes: a fall in total phospholipids, sphingomyelin, phosphatidylcholine, phosphatidic acid, a trend to increasing lysophosphatidylcholine. The shifts go in parallel with lipid peroxidation activation. Carbohydrate
Alexander von Tesmar et al.
Cell chemical biology, 24(10), 1216-1227 (2017-09-12)
In vitro reconstitution and biochemical analysis of natural product biosynthetic pathways remains a challenging endeavor, especially if megaenzymes of the nonribosomal peptide synthetase (NRPS) type are involved. In theory, all biosynthetic steps may be deciphered using mass spectrometry (MS)-based analyses of
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