133337
4-乙酰氨基苯甲酸
98%
别名:
对乙酰氨基苯甲酸
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关于此项目
线性分子式:
CH3CONHC6H4CO2H
化学文摘社编号:
分子量:
179.17
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
209-114-7
MDL number:
Beilstein/REAXYS Number:
390602
Quality Level
assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
259-262 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
CC(=O)Nc1ccc(cc1)C(O)=O
InChI
1S/C9H9NO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5H,1H3,(H,10,11)(H,12,13)
InChI key
QCXJEYYXVJIFCE-UHFFFAOYSA-N
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Yasuhiro Uno et al.
Biochemical pharmacology, 177, 113996-113996 (2020-04-28)
In humans, polymorphic N-acetyltransferases NAT1 and NAT2 are important enzymes that metabolize endogenous and exogenous compounds, including drugs. These enzymes exhibit considerable inter-individual variability in humans. The cynomolgus macaque is a nonhuman primate species that is widely used in drug
João Neres et al.
Bioorganic & medicinal chemistry, 15(5), 2106-2119 (2007-01-16)
Benzoic acid and pyridine derivatives inhibit recombinant trans-sialidase from Trypanosoma cruzi with I50 values between 0.4 and 1mM. The best compounds, 4-acetylamino-3-hydroxymethylbenzoic acid and 5-acetylamino-6-aminopyridine-2-carboxylic acid, provide new leads to inhibitors not containing the synthetically complex sialic acid structure. The
J A Kovacs et al.
Antimicrobial agents and chemotherapy, 37(6), 1227-1231 (1993-06-01)
Isoprinosine has been reported to decrease progression to AIDS, primarily by preventing Pneumocystis carinii pneumonia (PCP), in human immunodeficiency virus-infected patients, but the mechanism of action is unknown. para-Acetamidobenzoic acid (PAcBA), one component of isoprinosine, is structurally related to para-aminobenzoic
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 133337-25G | 04061838729460 |