4-Piperidinamine,n-methyl-n-[3-(1-methylethoxy)-2-pyridinyl]-1-[[5-[(methylsulfonyl)amino]-1h-indol-2-yl]carbonyl]

Modify Date: 2026-02-20 11:03:56

4-Piperidinamine,n-methyl-n-[3-(1-methylethoxy)-2-pyridinyl]-1-[[5-[(methylsulfonyl)amino]-1h-indol-2-yl]carbonyl] Structure
4-Piperidinamine,n-methyl-n-[3-(1-methylethoxy)-2-pyridinyl]-1-[[5-[(methylsulfonyl)amino]-1h-indol-2-yl]carbonyl] structure
Common Name 4-Piperidinamine,n-methyl-n-[3-(1-methylethoxy)-2-pyridinyl]-1-[[5-[(methylsulfonyl)amino]-1h-indol-2-yl]carbonyl]
CAS Number 179556-87-7 Molecular Weight 485.6
Density N/A Boiling Point N/A
Molecular Formula C24H31N5O4S Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name 4-Piperidinamine,n-methyl-n-[3-(1-methylethoxy)-2-pyridinyl]-1-[[5-[(methylsulfonyl)amino]-1h-indol-2-yl]carbonyl]

 Chemical & Physical Properties

Molecular Formula C24H31N5O4S
Molecular Weight 485.6
InChIKey GOVNLCZMXFXJSM-UHFFFAOYSA-N
SMILES CC(C)OC1=C(N=CC=C1)N(C)C2CCN(CC2)C(=O)C3=CC4=C(N3)C=CC(=C4)NS(=O)(=O)C

 Bioassay

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Name: In vitro inhibition of HIV-1 reverse transcriptase at 100 uM.
Source: ChEMBL
Target: Reverse transcriptase/RNaseH
External Id: CHEMBL800644
Name: Effective dose ofcompound against replication of HIV-1 D34 isolate in human PBMC was ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL763518
Name: Half life upon microsomal incubation
Source: ChEMBL
Target: N/A
External Id: CHEMBL635112
Name: HIV Enzyme Data
Source: NIAID
Target: N/A
External Id: HIV Enzyme Data
Name: Fold resistance expressed as ratio of IC 50 mutant Y181C vs WT RT
Source: ChEMBL
Target: N/A
External Id: CHEMBL844096
Name: Fold resistance expressed as ratio of IC 50 mutant P236L vs WT RT
Source: ChEMBL
Target: N/A
External Id: CHEMBL844095
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