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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099494Generated: October 25, 2026

Iniparib → Benzamide

https://huagongshe.com/reaction/1099494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIniparibHCID 9796068—
SolventAcetonitrileHCID 6342—
ProductBenzamideHCID 2331—

Reaction Steps

Plasma samples were obtained from dog, rat and mouse studies, in which animals were administered 4-iodo-3-nitrobenzamide (BA). Plasma and tumor samples were prepared for HPLC injection by precipitating plasma (50 μl) with 3× volumes (150 μl) of acetonitrile. Tissue samples were prepared for HPLC injection by adding 1 μl of acetonitrile per mg of tissue, then homogenizing with an electric homogenizer. Following centrifugation, 150 μl of each supernatant was evaporated to dryness, reconstituted in 50 μl of 0.2% formic acid in water and analyzed by chromatography and mass spectrometry techniques (LC/MS/MS conditions). LC/MS/MS conditions are: HPLC (Shimadzu VP System); Mobile Phase: 0.2% formic acid in water (A) and 0.18% formic acid in methanol (B); Column: 1×50 mm Thermo BetaBasic C18 column; Injection volume: 25 μL; Gradient: 0-60% B in 30 minutes; Flow Rate: 100 μL/min; Mass Spectrometer: Applied Biosystems/MDS SCIEX Q-STAR; Interface: IonSpray split at 1/10; Parent Ion Scan: TOF Positive from 200-900 amu; Product Ion Scan: TOF Product Ion from 60-900 amu of most intense Ion in Parent Ion Scan; TOF calibration: Externally calibrated using Renin Substrate. Results of metabolite identification from dog and mouse plasma are depicted in Tables 1-3, as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143447B2
Source datasetuspto-grants-2012_03
ORD IDord-3dfc067080a6466a9648683c18470a18
Source noteuspto-grants-2012_03