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127671

3-Aminobenzoic acid

Name: 3-Aminobenzoic acid
Brand: ALDRICH

98%, for peptide synthesis

Synonym(s):

3-Aminobenzenecarboxylic acid, 3-Carboxyaniline, m-Aminobenzoic acid, Aniline-3-carboxylic acid

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About This Item

Linear Formula:

H₂NC₆H₄CO₂H

CAS Number:

99-05-8

Molecular Weight:

137.14

NACRES:

NA.22

PubChem Substance ID:

24847793

UNSPSC Code:

12352106

EC Number:

202-724-4

MDL number:

MFCD00007795

Beilstein/REAXYS Number:

471603

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Properties

Product Name

3-Aminobenzoic acid, 98%

Quality Level

100

assay

98%

reaction suitability

reaction type: solution phase peptide synthesis

mp

178-180 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cccc(c1)C(O)=O

InChI

1S/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)

InChI key

XFDUHJPVQKIXHO-UHFFFAOYSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3.

Lari Lehtiö et al.

Journal of medicinal chemistry, 52(9), 3108-3111 (2009-04-10)

Poly(ADP-ribose) polymerases (PARPs) activate DNA repair mechanisms upon stress- and cytotoxin-induced DNA damage, and inhibition of PARP activity is a lead in cancer drug therapy. We present a structural and functional analysis of the PARP domain of human PARP-3 in

Poly(adenosine diphosphate ribose) polymerase inhibition prevents necrosis induced by H2O2 but not apoptosis.

A J Watson et al.

Gastroenterology, 109(2), 472-482 (1995-08-01)

H2O2 causes DNA damage, which activates poly(adenosine diphosphate ribose) polymerase (PARP), a nuclear enzyme that uses nicotinamide adenine dinucleotide (NAD) as a substrate. When DNA strand breaks are extensive, consumption of NAD by PARP can cause adenosine triphosphate depletion. The

Simultaneous determination of substituent patterns in partially acid hydrolyzed O-Me/O-Me-d(3)-cellulose and quantification of the obtained oligomers by HPLC-ESI-MS.

Julia Cuers et al.

Carbohydrate research, 348, 55-63 (2011-12-17)

Substituent patterns in oligosaccharide derivatives obtained from methyl cellulose were determined up to DP10 by electrospray ionization mass spectrometry employing separation of the oligomer fractions by HPLC. Oligosaccharides were labeled with meta-aminobenzoic acid after perdeuteromethylation and partial hydrolysis of methyl

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Global Trade Item Number

SKU	GTIN
127671-500G	04061838725042
127671-25G	04061838725035
127671-100G	04061838725028