1124 Results for: "Ethyl-4-oxo-3-piperidinecarboxylate hydrochloride"

Supplier: Molekula

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Supplier: Merck

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: BIONET RESEARCH

1-(2-(Ammoniooxy)ethoxy)-3-(trifluoromethyl)benzene chloride

Supplier: Apollo Scientific

5-Aminolevulinic acid hydrochloride 97%

Supplier: ENZO LIFE SCIENCES

Antiviral, antibacterial, antiprotozoal, immunomodulating, and antineoplastic cytostatic anthraquinone derivative. Induces DNA damage by intercalating into DNA and inhibiting topoisomerase II. Induces interstrand DNA cross-links and DNA-protein cross-links in cellular systems. Has been shown to be an inhibitor of DNA methylation.

Supplier: Thermo Fisher Scientific

Chemical probes can be used to help establish the
relationship between a molecular target and the broader
biological consequences of modulating that target in cells
or organisms.

Supplier: Molekula

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Supplier: Merck

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Merck

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Merck

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: FLUOROCHEM

1-(2-(Ammoniooxy)ethoxy)-3-(trifluoromethyl)benzene chloride

Supplier: BACHEM BIOCHEMICA

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Supplier: COMBI-BLOCKS

4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid hydrochloride

Supplier: Merck

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Thermo Fisher Scientific

CAS No.: 5451-09-2

Supplier: Merck Millipore (Calbiochem‎)

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Uptima

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce Premium Grade EDC is our highest quality formulation of this popular carbodiimide crosslinker, specially characterized for applications where product integrity and risk minimization are paramount.

Supplier: Merck

ETHYL 1-BENZYL-3-OXO-4-PIPERIDINE-CARBOX YLATE HYDROCHLORIDE, TECH. 1 * 5 g

Supplier: Thermo Fisher Scientific

Cystamine dihydrochloride acts as an anti-infective agent, which is used in the treatment of urinary tract infections. It is also used as a radiation-protective agent that interferes with sulfhydryl enzymes. Further, it serves as a heparin antagonist and sulfhydryl modifying reagent. In addition to this, it is used as an inhibitor of TGase.

Supplier: Thermo Fisher Scientific

Mitoxantrone dihydrochloride 97%

Supplier: Cayman Chemical

ZZW-115 trihydrochloride ≥95%

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Merck

ETHYL 1-BENZYL-3-OXO-4-PIPERIDINE-CARBOX YLATE HYDROCHLORIDE, TECH. 1 * 25 g

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Molekula

Cystamine dihydrochloride

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®

Supplier: SIA ENAMINE

2-({2-OXO-2-[(2,3,4-TRIFLUOROPHENYL)AMINO]ETHYL}AMINO)-N-(2,3,4-TRIFLUOROPHENYL)ACETAMIDE HYDROCHLORIDE 1 * 1 g

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®