339598
4-氨基-3-羟基苯甲酸
97%
别名:
3-Hydroxy-4-aminobenzoic acid, 3-Hydroxy-PABA
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关于此项目
线性分子式:
H2NC6H3(OH)CO2H
化学文摘社编号:
分子量:
153.14
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
MDL number:
Beilstein/REAXYS Number:
509859
InChI
1S/C7H7NO3/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,9H,8H2,(H,10,11)
SMILES string
Nc1ccc(cc1O)C(O)=O
InChI key
NFPYJDZQOKCYIE-UHFFFAOYSA-N
assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
211-215 °C (lit.)
application(s)
peptide synthesis
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Kerim Babaoglu et al.
Nature chemical biology, 2(12), 720-723 (2006-10-31)
Fragment-based screens test multiple low-molecular weight molecules for binding to a target. Fragments often bind with low affinities but typically have better ligand efficiencies (DeltaG(bind)/heavy atom count) than traditional screening hits. This efficiency, combined with accompanying atomic-resolution structures, has made
Jinkyu Park et al.
Journal of hazardous materials, 371, 243-252 (2019-03-11)
Carboxylate-functionalized organic nanocrystals (ONCs) derived from perylene diimide or naphthalene diimide were synthesized and carefully characterized as novel high-capacity uranium (U(VI)) sorbents. Adsorption studies using uranyl ions demonstrated that the carboxyl and hydroxyl groups on the surface of the ONCs
Falicia Goh et al.
Microbial cell factories, 19(1), 71-71 (2020-03-21)
Notonesomycin A is a 32-membered bioactive glycosylated macrolactone known to be produced by Streptomyces aminophilus subsp. notonesogenes 647-AV1 and S. aminophilus DSM 40186. In a high throughput antifungal screening campaign, we identified an alternative notonesomycin A producing strain, Streptomyces sp.
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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