133337
4-Acetamidobenzoic acid
98%
Synonym(s):
N-Acetyl-PABA
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About This Item
Linear Formula:
CH3CONHC6H4CO2H
CAS Number:
Molecular Weight:
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
B Barbieri et al.
Biochimica et biophysica acta, 1257(2), 157-166 (1995-07-13)
We have previously reported that human lymphoid cells, such as peripheral blood mononuclear leukocytes (PBML) and the T-cell leukemia line Jurcat, synthesize p-acetamidobenzoic acid from p-aminobenzoic acid (PABA) and a two carbon fragment from arachidonic acid (AA), conceivably derived from