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Merck
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文件

278998

Sigma-Aldrich

2-氨基-5-羟基苯甲酸

98%

别名:

5-羟基邻氨苯甲酸

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About This Item

线性分子式:
HOC6H3(NH2)CO2H
CAS号:
394-31-0
分子量:
153.14
Beilstein:
2803663
MDL號碼:
MFCD00007870
分類程式碼代碼:
12352106
eCl@ss:
32160406
PubChem物質ID:
24856846
NACRES:
NA.22

化驗

98%

形狀

solid

反應適用性

reaction type: solution phase peptide synthesis

mp

247 °C (dec.) (lit.)

應用

peptide synthesis

SMILES 字串

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 密鑰

HYNQTSZBTIOFKH-UHFFFAOYSA-N

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相关类别

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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[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
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
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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