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Merck
CN

W505404

p -茴香酸

≥99%

别名:

4-甲氧基苯甲酸, 对甲氧基苯甲酸, 龙血酸

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关于此项目

线性分子式:
CH3OC6H4CO2H
化学文摘社编号:
分子量:
152.15
EC Number:
202-818-5
UNSPSC Code:
12164502
Flavis number:
8.071
Beilstein/REAXYS Number:
508910
MDL number:
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InChI key

ZEYHEAKUIGZSGI-UHFFFAOYSA-N

InChI

1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)

SMILES string

COc1ccc(cc1)C(O)=O

assay

≥99%

mp

182-185 °C (lit.)

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Features and Benefits

味甜,可令人晕厥、恶心、脸色苍白

存储类别

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

365.0 °F - closed cup

flash_point_c

185 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Hyunshun Shin et al.
Bioorganic & medicinal chemistry, 15(7), 2617-2623 (2007-02-14)
The first committed step in lipid A biosynthesis is catalyzed by uridine diphosphate-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase (LpxC), a zinc-dependent deacetylase, and inhibitors of LpxC may be useful in the development of antibacterial agents targeting a broad spectrum of Gram-negative bacteria. Here, we
Jean J K Bankeu et al.
Journal of natural products, 74(6), 1370-1378 (2011-05-31)
Phytochemical investigation of the figs of Ficus mucuso led to the isolation of three new isoflavone dimer derivatives, mucusisoflavones A-C (1-3), together with 16 known compounds. Some of the isolates were tested in vitro for their inhibitory properties toward β-glucuronidase
Souichi Nakashima et al.
Bioorganic & medicinal chemistry, 18(6), 2337-2345 (2010-03-02)
The methanolic extract from the whole plants of Anastatica hierochuntica, an Egyptian herbal medicine, was found to inhibit melanogenesis in theophylline-stimulated murine B16 melanoma 4A5 cells. Among the constituents isolated, anastatin A, silybin A, isosilybins A and B, eriodictyol, luteolin
Fabrizio Carta et al.
Bioorganic & medicinal chemistry letters, 21(8), 2521-2526 (2011-03-16)
The inhibition of the β-carbonic anhydrases (CAs, EC 4.2.1.1) from the pathogenic fungi Cryptococcus neoformans (Can2) and Candida albicans (Nce103) with a series of 25 branched aliphatic and aromatic carboxylates has been investigated. Human isoforms hCA I and II were
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

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