ELZEGURAN
UNII 5DBG4GC6MX

Substance Identification & Data

This profile provides standardized clinical and technical data for Elzeguran, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 5DBG4GC6MX.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 2724283-08-1 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
5DBG4GC6MX
CAS Registry Number
2724283-08-1
RxNorm Concept ID
N/A

Detailed Substance Profile

Preferred Name
ELZEGURAN
Official standardized name for this substance within the FDA UNII nomenclature system.
INN ID
14150
Sequential identifier assigned via the WHO International Nonproprietary Name program.
Substance Type
Elzeguran
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Elzeguran. 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

Elzeguran

Common Names & Synonyms

RNA (human/Macaca fascicularis proprotein convertase subtilisin kexin 9 gene PCSK9-targeting guide RNA PCS-gRNA009)
elzeguran [INN]
guide RNA (gRNA) targeting a splice donor site at the junction of exon 1 and intron 1 of the human proprotein convertase subtilisin/kexin type 9 (PCSK9) gene. all-P-ambo-2′-O-methyl-P-thiocytidylyl-(3′→5′)-2′-Omethyl-P-thiocytidylyl-(3′→5′)-2′-O-methyl-Pthiocytidylyl-( 3′→5′)-guanylyl-(3′→5′)-cytidylyl-(3′→5′)-adenylyl-(3′→5′)-cytidylyl-(3′→5′)-cytidylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-guanylyl-(3′→5′)-guanylyl-(3′→5′)-cytidylyl-(3′→5′)-guanylyl-(3′→5′)-cytidylyl-(3′→5′)-adenylyl-(3′→5′)-guanylyl-(3′→5′)-cytidylyl-(3′→5′)-guanylyl-(3′→5′)-guanylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-adenylyl-(3′→5′)-guanylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-guanylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-2′-O-methyladenylyl-(3′→5′)-guanylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-adenylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-adenylyl-(3′→5′)-2′-Omethyluridylyl-( 3′→5′)-adenylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-guanylyl-(3′→5′)-uridylyl-(3′→5′)-2′-Omethylcytidylyl-( 3′→5′)-2′-O-methylcytidylyl-(3′→5′)-guanylyl-(3′→5′)-uridylyl-(3′→5′)-uridylyl-(3′→5′)-adenylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-Omethylcytidylyl-( 3′→5′)-adenylyl-(3′→5′)-adenylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-Omethyluridylyl-( 3′→5′)-2′-O-methyluridylyl-(3′→5′)-guanylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-Omethyladenylyl-( 3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-guanylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-Omethylcytidylyl-( 3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methyladenylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-Omethylguanylyl-( 3′→5′)-2′-O-methyluridylyl-(3′→5′)-2′-O-methylguanylyl-(3′→5′)-2′-O-methylcytidylyl-(3′→5′)-2′-O-methyl-P-thiouridylyl-(3′→5′)-2′-O-methyl-Pthiouridylyl-( 3′→5′)-2′-O-methyl-P-thiouridylyl-(3′→5′)-2′-O-methyluridine