Guanethidine

SKU:BHB21902681
Research Validated
Overview
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Guanethidine (CAS 55-65-2) is a bioactive small molecule supplied as a solid. Relevant to GPCR/G Protein and Neuronal Signaling research. Molecular formula C10H22N4, molecular weight 198.31 g/mol.
CAS Number 55-65-2
Molecular Weight 198.31 g/mol
Form Solid
Storage See Certificate of Analysis
Options selector
Catalog no. Size
HY-B1251-50MG 50 mg
HY-B1251-100MG 100 mg
HY-B1251-250MG 250 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 50 mg, 100 mg, 250 mg
  • Lead time: confirmed on inquiry for every option.
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: store as stated on the Certificate of Analysis; contact us if you need the condition before ordering.
Field Specification
CAS no. 55-65-2
Applications
  • Functional Assay (In Vitro)
Molecular weight 198.31
Molecular formula C10H22N4
SMILES NC(NCCN1CCCCCCC1)=N
Form Solid
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-B1251
Main SKU BHB21902681
Bioactive Small Molecules

Compound Overview

Guanethidine was synthesized in 1959. It is thought to lower blood pressure by interfering with the metabolism of chemical transmitter substances in post-ganglionic sympathetic nerve fibres. It is supplied as a solid (C10H22N4, MW 198.31).

Physical & Chemical Properties

CAS Number 55-65-2
Molecular Formula C10H22N4
Molecular Weight 198.31 g/mol
Appearance Solid
SMILES NC(NCCN1CCCCCCC1)=N
Signaling Pathway GPCR/G Protein; Neuronal Signaling
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. P Dubový, etal. Local chemical sympathectomy of rat bone marrow and its effect on marrow cell composition.

[2]. Waldiceu A.VerriJr, etal. Antigen-induced inflammatory mechanical hypernociception in mice is mediated by IL-18. Brain Beha

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

Sympathetic fiber ablation is associated with loss of rat endothelial cell marker (RECA), but guanethidine had no significant effect on endothelial cell and mesenchymal stem cell survival in vitro[1].

In Vivo

Guanethidine (30 mg/kg, s.c., 1 h), acting as a sympathetic blocker, did not affect IL-18 hypernociception in TNFR1(-/-) mice[2].

Animal ModelWild-type (WT) Balb/c,TNFR1(-/-)and IFN-γ-γ(-/-) mice[2].
Dosage30 mg/kg
AdministrationGuanethidine (30 mg/kg, s.c., 1 h, diluted in saline)
ResultPre-treatment with guanethidine (sympathetic blocker) unaffected IL-18 hypernociception in TNFR1(-/-) mice.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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A gatekeeper sympathetic control of lacrimal tear secretion and dry eye onset through the NA-Adra1a-Ucp2 pathway. Nat Commun 2025 Jun 5;16(1):5215. PMID: 40473608

A stress-responsive neurovascular axis shapes skin immune accessibility. iScience 2026 Feb 23;29(3):115122. PMID: 41852725

Authorea. September 19, 2022.

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