SUVN-502

Modify Date: 2025-08-25 12:24:22

SUVN-502 Structure
SUVN-502 structure
Common Name SUVN-502
CAS Number 701205-60-9 Molecular Weight 478.40
Density N/A Boiling Point N/A
Molecular Formula C21H24BrN3O3S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of SUVN-502


Masupirdine free base (SUVN-502 free base) is a potent, selective, orally bioavailable, and brain penetrant 5-HT6 receptor antagonist (Ki of 2.04 nM for human 5-HT6 receptor). Masupirdine free base (SUVN-502 free base) shows high selectivity over 5-HT2A receptor and other 100 target sites, and has potential for treatment of Alzheimer's disease[1].

 Names

Name Masupirdine free base

 SUVN-502 Biological Activity

Description Masupirdine free base (SUVN-502 free base) is a potent, selective, orally bioavailable, and brain penetrant 5-HT6 receptor antagonist (Ki of 2.04 nM for human 5-HT6 receptor). Masupirdine free base (SUVN-502 free base) shows high selectivity over 5-HT2A receptor and other 100 target sites, and has potential for treatment of Alzheimer's disease[1].
Related Catalog
Target

Ki: 2.04 nM (human 5-HT6 receptor)[1]

References

[1]. Nirogi R, et al. Discovery and Development of 1-[(2-Bromophenyl)sulfonyl]-5-methoxy-3-[(4-methyl-1-piperazinyl)methyl]-1H-indole Dimesylate Monohydrate (SUVN-502): A Novel, Potent, Selective and Orally Active Serotonin 6 (5-HT6) Receptor Antagonist for Potential Treatment of Alzheimer's Disease. J Med Chem. 2017 Mar 9;60(5):1843-1859.

 Chemical & Physical Properties

Molecular Formula C21H24BrN3O3S
Molecular Weight 478.40
InChIKey GWCYPEHWIZXYFZ-UHFFFAOYSA-N
SMILES COc1ccc2c(c1)c(CN1CCN(C)CC1)cn2S(=O)(=O)c1ccccc1Br
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

SUVN-502 suppliers

SUVN-502 price

Related Compounds: More...
SUVN-502 mesylate
1791396-46-7
SUVN-502 mesylate hydrate
1791396-45-6
SUVN-911(compound 9h)
2414674-71-6
SUVN-G3031
1394808-82-2
4-[2-[(2S,3R,4R)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-6-heptyl-4-hydroxybenzoyl]oxy-2-heptyl-6-hydroxybenzoic acid
120634-85-7
2-[[5-[4-(dimethylsulfamoyl)phenyl]-8-methyl-2-oxo-7,9-dihydro-6H-pyrrolo[3,2-h]isoquinolin-3-yl]amino]oxy-4-hydroxybutanoic acid
254751-28-5
NCT-502
1542213-00-2
GNE-502
1953134-16-1
ARRY-502
1202891-16-4
4-({2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-thiazol-5-yl}formamido)-3-hydroxybutanoic acid
2172058-38-5
2-(1-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-thiazole-5-amido}cyclopropyl)acetic acid
2172489-46-0
2-({2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-4-methyl-1,3-thiazol-5-yl}formamido)-3-hydroxy-2-methylpropanoic acid
2172171-35-4
1-{2-methyl-5H,6H,7H-cyclopenta[d]pyrimidine-4-carbonyl}-4-(3-methylphenyl)piperazine
2770582-47-1
1-(5-chloro-2-methylphenyl)-4-{2-methyl-5H,6H,7H-cyclopenta[d]pyrimidine-4-carbonyl}piperazine
2770641-09-1
3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,3-thiazole-5-carbonyl]-2-methyl-1,3-thiazolidine-4-carboxylic acid
2171547-91-2
Ethyl4-bromo-5-chlorothiophene-3-carboxylate
2297850-30-5
tert-butyl N-[1-(2-methyl-1,3-thiazol-4-yl)-1-oxopropan-2-yl]carbamate
2009710-23-8
N-(cyclohexylmethyl)-2-methyl-5H,6H,7H-cyclopenta[d]pyrimidine-4-carboxamide
2770639-85-3
2-{[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylbutanamido]methyl}cyclopropane-1-carboxylic acid
2172058-50-1