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284572

Sigma-Aldrich

4-Aminobenzamide

98%

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About This Item

Formule linéaire :
H2NC6H4CONH2
Numéro CAS:
2835-68-9
Poids moléculaire :
136.15
Numéro CE :
220-612-3
Numéro MDL:
MFCD00007999
Code UNSPSC :
12352100
ID de substance PubChem :
24857167
Nomenclature NACRES :
NA.22

Pureté

98%

Forme

solid

Pf

181-183 °C (lit.)

Chaîne SMILES 

NC(=O)c1ccc(N)cc1

InChI

1S/C7H8N2O/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H2,9,10)

Clé InChI

QIKYZXDTTPVVAC-UHFFFAOYSA-N

Catégories apparentées

Application

4-Aminobenzamide was used as a poly(ADP-ribose)polymerase (PADPRP) inhhibitor to study the death of target cells by cytotoxic effector cells using the nuclear enzyme poly(ADP-ribose)polymerase (PADPRP).

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H319,H335

Classification des risques

Eye Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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D Monti et al.
Biochemical and biophysical research communications, 199(2), 525-530 (1994-03-15)
The death of target cells by cytotoxic effector cells is a relevant biological phenomenon, where cells are activated and a very quick apoptotic program occurs. In order to test the hypothesis that the nuclear enzyme poly(ADP-ribose)polymerase (PADPRP) plays a role
P Burgman et al.
Radiation research, 116(3), 406-415 (1988-12-01)
The purpose of this study was to investigate a possible involvement of poly(ADP-ribosyl)ation reactions in hyperthermic cell killing and hyperthermic DNA strand-break induction and repair in HeLa S3 cells. The inhibitors of poly(ADP-ribose) polymerase, 3-aminobenzamide (3AB) and 4-aminobenzamide (4AB), were
E Ben-Hur et al.
Radiation research, 97(3), 546-555 (1984-03-01)
Postirradiation incubation of V79 Chinese hamster cells with inhibitors of poly(ADP-ribose) synthesis was found to potentiate the killing of cells by X rays. Potentiation increased with incubation time and with concentration of the inhibitor. Preirradiation incubation had only a small
Jamie Lajiness et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 5(3), 216-226 (2009-05-16)
Imidazole and pyrrole-containing polyamides belong to an important class of compounds that can be designed to target specific DNA sequences, and they are potentially useful in applications of controlling gene expression. The extent of polyamide curvature is an important consideration
R Laffranchi et al.
Experimental cell research, 237(1), 217-222 (1998-01-07)
Interferon-gamma is among the cytokines which have been implicated as effector molecules of beta-cell destruction in autoimmune diabetes. Its mechanism of action is, however, largely unknown. In the present study rat pancreatic beta-cells, INS-1, were incubated with rat interferon-gamma (rIRN-gamma)
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