You Searched For: Ethyl-3-amino-3-methylbutanoate+hydrochloride


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


Supplier: Thermo Scientific Chemicals
Description: D(-)-2-Phenylglycine ethyl ester hydrochloride ≥98%
Supplier: Thermo Scientific Chemicals
Description: L-Phenylalanine ethyl ester hydrochloride 98%
Catalog Number: (89152-474)
Supplier: Enzo Life Sciences
Description: Na⁺ channel blocker and class I antiarrhythmic.

Supplier: TCI America
Description: Roxatidine Acetate Hydrochloride, Purity: >98.0%(HPLC)(T), Cas number: 93793-83-0, Molecular Formula: C19H28N2O4.HCl, MW: 384.90, Synonyms: 2-Acetoxy-N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]acetamide Hydrochloride, Appearance: Crystal - Powder, Size: 200MG

SDS

Supplier: Thermo Scientific Chemicals
Description: L-type calcium channel blocker
Supplier: Thermo Scientific Chemicals
Description: An A2A Adenosine receptor agonist. CGS 21680 hydrochloride is currently used in research in studying neuronal transmission, also in respiration.
Supplier: Thermo Scientific Chemicals
Description: Inhibitor of HMG-CoA reductase. Induces apoptosis
Supplier: Enzo Life Sciences
Description: Antiviral, antibacterial, antiprotozoal, immunomodulating, and antineoplastic cytostatic anthraquinone derivative

Catalog Number: (CA80057-044)
Supplier: MilliporeSigma
Description: An antibiotic that acts as a potent inhibitor of HMG-CoA reductase, thus suppressing Ras farnesylation

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: Bachem Americas
Description: Sequence: H-Pen-OH

Supplier: TCI America
Description: CAS Number: 516-06-3
MDL Number: MFCD00004267
Molecular Formula: C5H11NO2
Molecular Weight: 117.15
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Color: White
Melting point (°C): 295
Supplier: G-Biosciences
Description: EDC is a heterobifunctional, water-soluble, zero-length carbodiimide crosslinker that is used to couple carboxyl groups to primary amines. EDC activates carboxyl groups first and forms amine reactive O-acylisourea imtermediate that spontaneously reacts with primary amines to form an amide bond and isourea by-product.

Supplier: Thermo Scientific Chemicals
Description: DL-Valine 99%
Supplier: Thermo Scientific Chemicals
Description: N-Benzyloxycarbonyl-L-valine N-succinimidyl ester, 98%
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