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AB120791

Phentolamine hydrochloride, Non-selective alpha antagonist

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(6 Publications)

MW 317.8 Da, Purity >98%. Potent, reversible, non-selective α antagonist. Achieve your results faster with highly validated, pure and trusted compounds.

View Alternative Names

ADA1D_HUMAN, ADRA 1, ADRA1A, ADRA1R, Adra1d, Adrd1, Adrenergic alpha 1A receptor, Adrenergic alpha 1D receptor, Adrenergic receptor alpha 1d, Adrenergic receptor delta1, Adrenoceptor alpha 1D, Alpha-1, Alpha-1A adrenergic receptor, Alpha-1D adrenergic receptor, Alpha-1D adrenoceptor, Alpha-1D adrenoreceptor, Alpha-adrenergic receptor 1a, Alpha1DAR, DAR, Gpcr8, RA42, Spr8, dJ779E11.2

1 Images
Chemical Structure - Phentolamine hydrochloride, Non-selective alpha antagonist (AB120791)
  • Chemical Structure

Lab

Chemical Structure - Phentolamine hydrochloride, Non-selective alpha antagonist (AB120791)

2D chemical structure image of ab120791, Phentolamine hydrochloride, Non-selective alpha antagonist

Key facts

CAS number

73-05-2

Purity

>98%

Form

Solid

form

Molecular weight

317.8 Da

Molecular formula

C<sub>1</sub><sub>7</sub>H<sub>2</sub><sub>0</sub>ClN<sub>3</sub>O

PubChem

5702144

Nature

Synthetic

Solubility

Soluble in water to 50 mM

Biochemical name

Phentolamine hydrochloride

Biological description

Potent, reversible, non-selective α antagonist.

Canonical smiles

CC1=CC=C(C=C1)N(CC2=NCCN2)C3=CC(=CC=C3)O.Cl

InChi

InChI=1S/C17H19N3O.ClH/c1-13-5-7-14(8-6-13)20(12-17-18-9-10-19-17)15-3-2-4-16(21)11-15;/h2-8,11,21H,9-10,12H2,1H3,(H,18,19);1H

InChiKey

TUEJFGFQYKDAPM-UHFFFAOYSA-N

IUPAC Name

3-[N-(4,5-dihydro-1H-imidazol-2-ylmethyl)-4-methylanilino]phenol;hydrochloride

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
It is important to note that this product is reported to be light sensitive|Store in the dark|Store under desiccating conditions

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The alpha 1d adrenergic receptor also known as the alpha-1d adrenoceptor is a G-protein-coupled receptor with mass approximately 70 kDa. It plays a critical role in the modulation of physiological responses by binding catecholamines like norepinephrine and epinephrine. Alpha-1d adrenergic receptor is widely expressed in vascular smooth muscle heart liver and central nervous system. This receptor remains an important target for pharmacological research due to its involvement in various physiological processes.
Biological function summary

The alpha-1d adrenergic receptor promotes vasoconstriction and increases blood pressure through the activation of phospholipase C pathway resulting in calcium release from intracellular stores. It functions as part of a receptor complex that interacts with other alpha-1 adrenergic subtypes such as alpha-1a and alpha-1b adrenergic receptors differentiating their roles in tissue-specific actions. These receptor activities affect muscle contraction and influence systemic vascular resistance.

Pathways

This adrenergic receptor is engaged in the adrenergic signaling in cardiomyocytes and vascular smooth muscle contraction pathways. It facilitates communication between the signaling molecules and cellular responses. The alpha-1d adrenergic receptor partners with proteins like Gq/11 protein family which mediates signal transduction leading to its physiological effects. Interaction with other receptors such as beta-adrenergic receptors shapes the overall cardiovascular outcomes by providing a balance between constriction and relaxation.

The alpha-1d adrenergic receptor links to hypertension and benign prostatic hyperplasia where its modulation can influence disease progression and treatment outcomes. In hypertension dysregulation of alpha-1d adrenergic signaling may alter vascular tone and resistance contributing to elevated blood pressure. Connections with proteins such as phospholipase C confirm its involvement in the signaling cascade that affects these conditions. Modulation of this receptor activity offers therapeutic potential for related cardiovascular and urological disorders.

Product protocols

Publications (6)

Recent publications for all applications. Explore the full list and refine your search

Science advances 10:eadj9581 PubMed38669335

2024

Inputs to the locus coeruleus from the periaqueductal gray and rostroventral medulla shape opioid-mediated descending pain modulation.

Applications

Unspecified application

Species

Unspecified reactive species

Susan T Lubejko,Giulia Livrizzi,Stanley A Buczynski,Janki Patel,Jean C Yung,Tony L Yaksh,Matthew R Banghart

BioMed research international 2018:2925985 PubMed29511675

2018

Regulation of Spontaneous Contractions in Intact Rat Bladder Strips and the Effects of Hydrogen Peroxide.

Applications

Unspecified application

Species

Unspecified reactive species

Mingshuai Wang,Nianzeng Xing,Liyang Wu,Wen-Chu Huang,Zhenqun Xu,Guiming Liu

Redox biology 10:128-139 PubMed27744118

2016

The synthetic progestin norgestrel modulates Nrf2 signaling and acts as an antioxidant in a model of retinal degeneration.

Applications

Unspecified application

Species

Unspecified reactive species

Ashleigh M Byrne,Ana M Ruiz-Lopez,Sarah L Roche,Jennifer N Moloney,Alice C Wyse-Jackson,Thomas G Cotter

Neuroscience 193:72-9 PubMed21784134

2011

Nerve growth factor augments neuronal responsiveness to noradrenaline in cultured dorsal root ganglion neurons of rats.

Applications

Unspecified application

Species

Unspecified reactive species

Q Zhang,Y Tan

Archives of pharmacal research 33:479-89 PubMed20361315

2010

Phentolamine inhibits the pacemaker activity of mouse interstitial cells of Cajal by activating ATP-sensitive K+ channels.

Applications

Unspecified application

Species

Unspecified reactive species

Seung Whan Ahn,Sang Hun Kim,Jin Ho Kim,Seok Choi,Cheol Ho Yeum,Hee Wook Wie,Jae Myeong Sun,Insuk So,Jae Yeoul Jun

Proceedings of the National Academy of Sciences of the United States of America 94:11716-20 PubMed9326676

1997

Phentolamine block of KATP channels is mediated by Kir6.2.

Applications

Unspecified application

Species

Unspecified reactive species

P Proks,F M Ashcroft
View all publications

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