You Searched For: Verapamil+hydrochloride

Supplier: Thermo Scientific Chemicals

Description: Verapamil hydrochloride 99+%

Supplier: Adipogen

Description: Verapamil hydrochloride is an alpha-adrenergic receptor (alpha-AR) antagonist and calcium channel protein inhibitor that blocks the L-type Ca2+ channels in smooth and cardiac muscle cells. Verapamil is an antiarrhythmic agent and vasodilator known to reduce the renal clearance of digoxin and induce apoptosis in primary and metastatic colon adenocarcinoma human cell lines in vitro. It has been observed that verapamil can induce currents by itself, presumably by acting on the potassium and chloride leakage. Verapamil has also been used as an inhibitor of drug efflux pump proteins such as Mdr (P-glycoprotein). Verapamil is a substrate of CYP3A4 and CYP2C6. It is also used in fluorescent cell sorting for DNA content, as it blocks efflux of a variety of DNA-binding fluorophores such as Hoechst 33342. Recent research has shown verapamil to be an effective treatment for diabetes in animal models. Verapamil helps treat diabetes by limiting TXNIP expression.

Supplier: MP Biomedicals

Description: (±)-Verapamil Hydrochloride is a α1-antagonist and calcium channel modulator.

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Supplier: Ambeed

Description: Verapamil hydrochloride 99%

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Supplier: Adipogen

Description: alpha1-Adrenergic receptor (alpha-AR) antagonist. Prototypical calcium channel protein inhibitor that blocks the L-type Ca2+ channels in smooth and cardiac muscle cells. Vasodilator known to reduce the renal clearance of digoxin and used to control hypertension, angina, cardiac arrhythmia and vascular headaches. Apoptosis inducer in primary and metastatic colon adenocarcinoma human cell lines in vitro. Inhibitor of drug efflux pump proteins such as Mdr (P-glycoprotein) which are often over-expressed in certain tumor cell lines. Substrate of CYP3A4 and CYP2C6. Used in fluorescent cell sorting for DNA content, as it blocks efflux of a variety of DNA-binding fluorophores such as Hoechst 33342. Anti-diabetic in animal models by limiting TXNIP expression.

Supplier: Enzo Life Sciences

Description: Blocks slow voltage-sensitive L-type Ca2+ channels. Adrenergic antagonist. Inhibits platelet-activating factor and PMA-stimulated prostaglandin production in Kupffer cells. Induces apoptosis. In vitro resistance modifier in drug resistant human tumor cell lines.

Catalog Number: (80055-494)

Supplier: MilliporeSigma

Description: A derivative of papaverine that blocks Ca2+ channels (principally the L-type) in smooth and cardiac muscle cells

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Catalog Number: (77695-286)

Supplier: LGC Standards

Description: Organic Standard, Verapamil-d6 Hydrochloride

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Supplier: LGC Standards

Description: TRC Verapamil Hydrochloride

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Supplier: LGC Standards

Description: TRC Nor Verapamil Hydrochloride

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Catalog Number: (77990-664)

Supplier: LGC Standards

Description: TRC (R)-(+)-Nor Verapamil Hydrochloride

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Catalog Number: (77695-045)

Supplier: LGC Standards

Description: Organic Standard, alpha-Propyl-alpha-(1-demethylethyl)-Verapamil Hydrochloride

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Catalog Number: (77693-679)

Supplier: LGC Standards

Description: Verapamil Hydrochloride, LoGiCal, LGC Standards

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Catalog Number: (77990-668)

Supplier: LGC Standards

Description: TRC Nor Verapamil-d6 Hydrochloride

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Catalog Number: (77981-017)

Supplier: LGC Standards

Description: TRC D 517 Hydrochloride (Verapamil Impurity)

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Catalog Number: (10118-204)

Supplier: VWR

Description: L-Ornithine hydrochloride grade: reagent CAS Number: 3184-13-2 synonym(s): (S)?-?(+)?-?2, 5-?Diaminopentanoic Acid Hydrochloride, (S)?-?2, 5-?Diaminopentanoic Acid Monohydrochloride, L-Ornithine Monohydrochloride 500g

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