General
Preferred name
SR59230A
Synonyms
SR 59230A hydrochloride ()
SR59230A HCl ()
SR59230A (hydrochloride) ()
SR59230A hydrochloride ()
SR 59230A (hydrochloride) ()
P&D ID
PD050309
CAS
1135278-41-9
174689-38-4
174689-39-5
Tags
available
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION SR59230A hydrochloride is a potent, selective, and blood-brain barrier penetrating ¦Â3-adrenergic receptor antagonist[1] with IC50s of 40, 408, and 648 nM for ¦Â3, ¦Â1, and ¦Â2 receptors, respectively[2].
PRICE 98
DESCRIPTION SR59230A hydrochloride (SR59230A HCl) is a blood-brain permeable, selective and highly potent ??3-adrenergic receptor antagonist that inhibits ultradian brown adipose tissue thermogenesis and interrupts associated paroxysmal brain and body heating.
DESCRIPTION SR59230A is a potent, selective, and blood-brain barrier penetrating ¦Â3-adrenergic receptor antagonist[1] with IC50s of 40, 408, and 648 nM for ¦Â3, ¦Â1, and ¦Â2 receptors, respectively[2].
PRICE 157
DESCRIPTION SR59230A is a potent, selective antagonist of ??3-adrenergic receptor(??3, ??1, and ??2 receptors with IC50s of 40, 408, and 648 nM , respectively).
DESCRIPTION Potent and selective beta3 antagonist (Tocriscreen Plus)
DESCRIPTION Potent and selective β3 antagonist (Tocriscreen Total)
DESCRIPTION SR 59230A hydrochloride is a potent, selective and orally available β3 adrenoceptor antagonist (IC50 = 40, 408 and 648 nM for β3, β1 and β2 receptors, respectively). SR 59230A blocks MDMA-induced hyperthermia at low concentrations, while it blocks hyperthermia and also increases heat loss through an α1-AR antagonistic mechanism at high concentrations. (BOC Sciences Bioactive Compounds)
DESCRIPTION Positive allosteric modulator of GABAB receptors (Tocris Bioactive Compound Library)
DESCRIPTION SR59230A hydrochloride (SR59230A HCl) is a blood-brain permeable, selective and highly potent β3-adrenergic receptor antagonist that inhibits ultradian brown adipose tissue thermogenesis and interrupts associated paroxysmal brain and body heating. (TargetMol Bioactive Compound Library)
DESCRIPTION SR59230A is a potent, selective antagonist of β3-adrenergic receptor(β3, β1, and β2 receptors with IC50s of 40, 408, and 648 nM , respectively). (TargetMol Bioactive Compound Library)
Cell lines
0
Organisms
1
Compound Sets
14
Cayman Chemical Bioactives
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
Drug Repurposing Hub
Guide to Pharmacology
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
Tocriscreen Plus
Tocriscreen Total
External IDs
44
Properties
(calculated by RDKit )
Molecular Weight
325.2
Hydrogen Bond Acceptors
3
Hydrogen Bond Donors
2
Rotatable Bonds
7
Ring Count
3
Aromatic Ring Count
2
cLogP
3.66
TPSA
41.49
Fraction CSP3
0.43
Chiral centers
2.0
Largest ring
6.0
QED
0.82
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
7-TM Receptors
Target
β3-adrenergic receptor
Adrenergic Receptor
β3-adrenoceptor
ADRB1, ADRB2, ADRB3
Primary Target
Adrenergic ?3 Receptors
MOA
Antagonist
Adrenergic Receptor antagonist
Pathway
GPCR/G protein
Neuroscience
Neuronal Signaling
Source data