Cart
sales@molnova.com
Perospirone
CAS No. 150915-41-6
Perospirone( —— )
Catalog No. M18058 CAS No. 150915-41-6
Perospirone is an antagonist of serotonin 5HT2A receptors and dopamine D2 receptors. It also displays affinity towards 5HT1A receptors as a partial agonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
|
| 10MG | 41 | In Stock |
|
| 25MG | 75 | In Stock |
|
| 50MG | 133 | In Stock |
|
| 100MG | 229 | In Stock |
|
| 200MG | 319 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePerospirone
-
NoteResearch use only, not for human use.
-
Brief DescriptionPerospirone is an antagonist of serotonin 5HT2A receptors and dopamine D2 receptors. It also displays affinity towards 5HT1A receptors as a partial agonist.
-
DescriptionPerospirone is an antagonist of serotonin 5HT2A receptors and dopamine D2 receptors. It also displays affinity towards 5HT1A receptors as a partial agonist.
-
In Vitro——
-
In VivoAnimal Model:Male ICR mice (6 weeks old) weighing 25-30 g Dosage:1.0, 3.0 or 10.0 mg/kg Administration:Orally; daily; for 14 consecutive days Result:Significantly attenuated PCP-induced cognitive deficits in mice in a dose-dependent manner.
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetPARP
-
Recptor5-HT2A|D2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number150915-41-6
-
Formula Weight426.57
-
Molecular FormulaC23H30N4O2S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 5 mg/mL (11.72 mM)
-
SMILESO=C1[C@H]2CCCC[C@H]2C(=O)N1CCCCN1CCN(CC1)c1nsc2ccccc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Ishibashi T, Ohno Y. Perospirone hydrochloride: the novel atypical antipsychotic agent with high affinities for 5-HT2, D2 and 5-HT1A receptors[J]. Biogenic Amines, 2004, 18(3):307-317.
molnova catalog
related products
-
E7016
E7016 (GPI 21016) is an orally available PARP inhibitor that inhibits DNA repair and enhances tumor cell radiosensitivity both in vitro and in vivo.
-
Rucaparib phosphate
An inhibitor of PARP with Ki of 1.4 nM for PARP1 in a cell-free assay.
-
AZD-9574
AZD-9574 is a selective inhibitor of PARP1 at the sites of SSBs. AZD-9574 exhibits anti-cancer activities and can be used in studies about HRD+ breast cancer and advanced solid malignancies.
