LADEMIRSEN
UNII KKQ6AQN9LH

Substance Identification & Data

This profile provides standardized clinical and technical data for Lademirsen, uniquely identified by the FDA Unique Ingredient Identifier (UNII) KKQ6AQN9LH.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 1404019-95-9 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code

KKQ6AQN9LH

CAS Registry Number

1404019-95-9

RxNorm Concept ID

N/A

Detailed Substance Profile

Preferred Name

LADEMIRSEN

Official standardized name for this substance within the FDA UNII nomenclature system.

NCI Thesaurus

C170089

National Cancer Institute reference terminology for clinical and research data.

INN ID

10800

Sequential identifier assigned via the WHO International Nonproprietary Name program.

USAN ID

DE-172

Identifier assigned by the United States Adopted Names Council.

Substance Type

nucleicAcid

ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Lademirsen. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

LADEMIRSEN

Common Names & Synonyms

DNA, D(P-THIO)((2'-O-(2-METHOXYETHYL))RA-(2'-O,4'-C-((S)-ETHYLIDENE))RC-A-T-(2'-O,4'-C-((S)-ETHYLIDENE))RC-A-G-T-(2'-O,4'-C-((S)-ETHYLIDENE))RC-T-G-A-(2'-O,4'-C-((S)-ETHYLIDENE))RU-A-A-G-(2'-O,4'-C-((S)-ETHYLIDENE))RC-T-(2'-O-(2-METHOXYETHYL))RA)

LADEMIRSEN [INN]

LADEMIRSEN [USAN]

SAR-339375

Systematic Nomenclature

ALL-P-AMBO-2'-O-(2-METHOXYETHYL)-P-THIOADENYLYL-(3'->5')-2'-O,4'-C-((1S)-ETHANE-1,1-DIYL)-P-THIOCYTIDYLYL-(3'->5')-2'-DEOXY-P-THIOADENYLYL-(3'->5')-P-THIOTHYMIDYLYL-(3'->5')-2'-O,4'-C-((1S)-ETHANE-1,1-DIYL)-P-THIOCYTIDYLYL-(3'->5')-2'-DEOXY-P-THIOADENYLYL-(3'->5')-2'-DEOXY-P-THIOGUANYLYL-(3'->5')-P-THIOTHYMIDYLYL-(3'->5')-2'-O,4'-C-((1S)-ETHANE-1,1-DIYL)-P-THIOCYTIDYLYL-(3'->5')-P-THIOTHYMIDYLYL-(3'->5')-2'-DEOXY-P-THIOGUANYLYL-(3'->5')-2'-DEOXY-P-THIOADENYLYL-(3'->5')-2'-O,4'-C-((1S)-ETHANE-1,1-DIYL)-P-THIOURIDYLYL-(3'->5')-2'-DEOXY-P-THIOADENYLYL-(3'->5')-2'-DEOXY-PTHIOADENYLYL-( 3'->5')-2'-DEOXY-P-THIOGUANYLYL-(3'->5')-2'-O,4'-C-((1S)-ETHANE-1,1-DIYL)-P-THIOCYTIDYLYL-(3'->5')-PTHIOTHYMIDYLYL-( 3'->5')-2'-O-(2-METHOXYETHYL)ADENOSINE

SYS

DNA, D(P-THIO)((2'-O-(2-METHOXYETHYL))RA-(3'->4')-(2',5'-ANHYDRO-6'-DEOXY-4'-C-(HYDROXYMETHYL)-.ALPHA.-L-MANNOFURANO)C-A-T-(3'->4')-(2',5'-ANHYDRO-6'-DEOXY-4'-C-(HYDROXYMETHYL)-.ALPHA.-L-MANNOFURANO)C-A-G-T-(3'->4')-(2',5'-ANHYDRO-6'-DEOXY-4'-C-(HYDROXYMETHYL)-.ALPHA.-L-MANNOFURANO)C-T-G-A-(3'->4')-(2',5'-ANHYDRO-6'-DEOXY-4'-C-(HYDROXYMETHYL)-.ALPHA.-L-MANNOFURANO)U-A-A-G-(3'->4')-(2',5'-ANHYDRO-6'-DEOXY-4'-C-(HYDROXYMETHYL)-.ALPHA.-L-MANNOFURANO)C-T-(2'-O-(2-METHOXYETHYL))RA)

SYS