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Benzamide

🥰Excellent
Catalog No. T6780Cas No. 55-21-0
Alias Phenylcarboxyamide, Benzoylamide, Amid kyseliny benzoove

Benzamide (Amid kyseliny benzoove), an inhibitor of poly(ADP-ribose) polymerase, is a derivative of benzoic acid.

Benzamide

Benzamide

🥰Excellent
Purity: 99.66%
Catalog No. T6780Alias Phenylcarboxyamide, Benzoylamide, Amid kyseliny benzooveCas No. 55-21-0
Benzamide (Amid kyseliny benzoove), an inhibitor of poly(ADP-ribose) polymerase, is a derivative of benzoic acid.
Pack SizePriceAvailabilityQuantity
50 mg$30In Stock
100 mg$40In Stock
200 mg$56In Stock
500 mg$92In Stock
1 g$133In Stock
1 mL x 10 mM (in DMSO)$39In Stock
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Purity:99.66%
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Product Introduction

Bioactivity
Description
Benzamide (Amid kyseliny benzoove), an inhibitor of poly(ADP-ribose) polymerase, is a derivative of benzoic acid.
Targets&IC50
PARP:3.3 μM
In vitro
Benzamide, an inhibitor of PARP is protective against excitatory amino acid-induced cell death in primary cultures of neurons derived from neonatal rat brain. In addition, benzamide has more recently been shown to partially prevent the loss of dopaminergic cells and the increase in reactive gliosis caused by METH in vitro in fetal rat mesencephalic cells in culture[1]. Benzamide prevents transformation in a cell cycle-specific manner, maximal prevention coinciding with early S phase, also characteristic of maximal susceptibility to transformation[2].
In vivo
PARP inhibitor benzamide is neuroprotective in C57Bl/6N mice against different types of neurotoxicities and without affecting body temperature[2]. Benzamide treatment significantly decreases the iNOS expression and number of apoptotic neurons and thereby improves the neuronal survival and memory during GCI. Benzamide administration (160 mg/kg i.p.) does not induce hypothermia and reaches the CNS in 30 min in the concentration range of 0.09-0.64 mM, at which, it shows neuroprotection[3].
Cell Research
Exposure to carcinogens and benzamide is done 10 hr after the release of the metabolically induced G1/S block and exposure lasts 10 hr, followed by three washings and refeeding with fresh media. (Only for Reference)
AliasPhenylcarboxyamide, Benzoylamide, Amid kyseliny benzoove
Chemical Properties
Molecular Weight121.14
FormulaC7H7NO
Cas No.55-21-0
SmilesNC(=O)C1=CC=CC=C1
Relative Density.1.341 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (371.47 mM)
Ethanol: 23 mg/mL (189.9 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM8.2549 mL41.2746 mL82.5491 mL412.7456 mL
5 mM1.6510 mL8.2549 mL16.5098 mL82.5491 mL
10 mM0.8255 mL4.1275 mL8.2549 mL41.2746 mL
20 mM0.4127 mL2.0637 mL4.1275 mL20.6373 mL
50 mM0.1651 mL0.8255 mL1.6510 mL8.2549 mL
100 mM0.0825 mL0.4127 mL0.8255 mL4.1275 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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