You Searched For: Ethyl+L-histidinate·HCl


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Supplier: Enzo Life Sciences
Description: A novel, selective inhibitor of receptor-mediated calcium entry. It inhibits receptor-mediated calcium entry in stimulated platelets (IC50=8-12µM) neutrophils and endothelial cells at concentrations which do not affect internal Ca2+ release. Note, in some cells SK&F 96365 can activate a novel Ca2+ entry pathway. Blocks TRPC3 and TRPC6 activation. Inhibits the histamine-induced formation of nitric oxide in human endothelial cells.

Supplier: Thermo Scientific Chemicals
Description: Nɑ-Benzoyl-L-arginine ethyl ester hydrochloride ≥98%
Supplier: Thermo Scientific Chemicals
Supplier: Thermo Scientific Chemicals
Description: L-Alanine ethyl ester hydrochloride ≥98%
Supplier: TCI America
Description: CAS Number: 2645-08-1
MDL Number: MFCD00012579
Molecular Formula: C15H22N4O3
Molecular Weight: 342.82
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 130
Specific rotation [a]20/D: -17 deg (C=2, H2O)
Catalog Number: (TCT3102-5G)
Supplier: TCI America
Description: Thioridazine Hydrochloride, Purity/Analysis Method: >98.0%(HPLC), CAS Number: 130-61-0, Molecular formula: C21H26N2S2. HCl, Molecular weight: 407.03, Synonym: 10-[2-(1-Methylpiperidin-2-yl)ethyl]-2-(methylthio)-10H-phenothiazine Hydrochloride, Size: 5G

Supplier: Thermo Scientific Chemicals
Description: Ethyl-4-oxo-3-piperidinecarboxylate hydrochloride 97%
Supplier: Thermo Scientific Chemicals
Description: L-Lysine ethyl ester dihydrochloride 99%
Supplier: Thermo Scientific
Description: 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: Thermo Scientific
Description: 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: Thermo Scientific Chemicals
Description: Crystalline.
Supplier: Thermo Scientific Chemicals
Description: An L-type calcium channel blocker
Catalog Number: (CAAAJ60937-MA)
Supplier: Thermo Scientific Chemicals
Description: Inhibits receptor-mediated calcium influx

Catalog Number: (89152-442)
Supplier: Enzo Life Sciences
Description: Ca2+ channel inhibitor


Catalog Number: (CA80058-638)
Supplier: MilliporeSigma
Description: SKF-96365 hydrochloride, Calbiochem®

Catalog Number: (TCT1470-010G)
Supplier: TCI America
Description: CAS Number: 1508-75-4
MDL Number: MFCD00058580
Molecular Formula: C17H20N2O2
Molecular Weight: 284.36
Purity/Analysis Method: >99.0% (HPLC,T)
Form: Crystal
Color: White
Melting point (°C): 98
Lambda max.: 254 nm (HCl aq.)

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