Name: Elvucitabine , DNA polymerase/reverse transcriptase inhibitor, CAS No.181785-84-2, DNA polymerase/reverse transcriptase inhibitor
SKU: E345120
Availability: InStock

Elvucitabine , DNA polymerase/reverse transcriptase inhibitor, CAS No.181785-84-2, DNA polymerase/reverse transcriptase inhibitor

CAS: 181785-84-2 Cat. No.: E345120 Formule: C₉H₁₀FN₃O₃ Poids moléculaire: 227.19

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Elvucitabine - CAS No(181785-84-2) by Aladdin Scientific

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DISPONIBLE À COMMANDE

Synonyms

beta-L-Fd4C | UNII-M09BUF90C0 | DB06236 | M09BUF90C0 | A14435 | .beta.-L-Fd4C | 4-amino-5-fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidin-2-one | ACH 126443 | Elvucitabine | ACH 126,443 | Q1334337 | 1,1-Dimethylethyl 2-formyl-1-piperid

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble Specifications Propriétés du produit Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Calculateurs de solution Avis

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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Elvucitabine is a novel, anti-viral agent.

Specifications

Synonymes

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Mécanisme d'action

DNA polymerase/reverse transcriptase inhibitor

Propriétés du produit

ALogP	-1.3

Noms et identifiants

Sourires canoniques	C1=CC(OC1CO)N2C=C(C(=NC2=O)N)F
IUPAC Name	4-amino-5-fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidin-2-one
InChIKey	HSBKFSPNDWWPSL-VDTYLAMSSA-N
INCHI	1S/C9H10FN3O3/c10-6-3-13(9(15)12-8(6)11)7-2-1-5(4-14)16-7/h1-3,5,7,14H,4H2,(H2,11,12,15)/t5-,7+/m1/s1
Isomères SMILES	C1=C[C@H](O[C@H]1CO)N2C=C(C(=NC2=O)N)F
Poids moléculaire	227.19
Reaxy-Rn	24713405
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24713405&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Classe Nucleoside and nucleotide analogues

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Classe	Nucleoside and nucleotide analogues
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Nucleoside and nucleotide analogues
Alternative Parents	Pyrimidones Aminopyrimidines and derivatives Halopyrimidines Aryl fluorides Hydropyrimidines Imidolactams Heteroaromatic compounds Dihydrofurans Azacyclic compounds Oxacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Primary alcohols Organofluorides Organopnictogen compounds
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Pyrimidine - Imidolactam - Dihydrofuran - Heteroaromatic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Amine - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

Homo sapiens (32628 Activities)

Poids moléculaire	227.190 g/mol
XLogP3	-1.300
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	227.071 Da
Monoisotopic Mass	227.071 Da
Topological Polar Surface Area	88.200 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	405.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1