General
Preferred name
MOXISYLYTE HYDROCHLORIDE
Synonyms
thymoxamine hydrochloride ()
Moxisylyte hydrochoride ()
Moxisylyte (hydrochloride) ()
P&D ID
PD000203
CAS
54-32-0
964-52-3
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 Moxisylyte (hydrochloride) is (alpha 1-blocker) antagonist, it can vasodilates cerebral vessels without reducing blood pressure. It is also used locally in the eye to reverse the mydriasis caused by phenylephrine and other sympathomimetic agents. [1][2]
PRICE 29
DESCRIPTION alpha1-Adrenoceptor antagonist (LOPAC library)
DESCRIPTION Moxisylyte hydrochloride is alpha 1-adrenoceptor antagonist. It can vasodilates cerebral vessels without reducing blood pressure. It is used as peripheral vasodilator. It is also used locally in the eye to reverse the mydriasis caused by phenylephrine. It is used as sympathomimetic agents. It has been listed. (BOC Sciences Bioactive Compounds)
DESCRIPTION Moxisylyte hydrochloride (Thymoxamine hydrochloride) is an alpha-adrenergic blocking agent that is used in Raynaud's disease. (TargetMol Bioactive Compound Library)
Compound Sets
8
BOC Sciences Bioactive Compounds
moxisylyte-hydrochloride-cas-964-52-3-item-80217
EU-OPENSCREEN Bioactive Compound Library
EOS100826
LOPAC library
MedChem Express Bioactive Compound Library
HY-B1435
Prestwick Chemical Library
Selleckchem Bioactive Compound Library
moxisylyte-hydrochloride
TargetMol Bioactive Compound Library
T0394
The Spectrum Collection
External IDs
21
Properties
(calculated by RDKit )
Molecular Weight
315.16
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
0
Rotatable Bonds
6
Ring Count
1
Aromatic Ring Count
1
cLogP
3.41
TPSA
38.77
Fraction CSP3
0.56
Chiral centers
0.0
Largest ring
6.0
QED
0.6
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Selectivity
alpha1
Target
Adrenergic Receptor
Pathway
GPCR/G protein
Neuroscience
Neuronal Signaling
Solubility
Soluble in ethanol (50 mg/ml)
Source data