Pirodavir - ≥98% , VP1 capsid protein disrupting agent, CAS No.124436-59-5, VP1 capsid protein disrupting agent

CAS: 124436-59-5 Cat. No.: P126501 Peso molecular: 369.46

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Pirodavir - ≥98% CAS No(124436-59-5) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY ≥98%

Synonyms

ethyl 4-(2-(1-(6-methylpyridazin-3-yl)piperidin-4-yl)ethoxy)benzoate | Acetosulfamin | Pirodavirum | Pirodavir (USAN/INN) | Sulfacitinum | BDBM50087765 | 4-{2-[1-(6-Methyl-pyridazin-3-yl)-piperidin-4-yl]-ethoxy}-benzoic acid ethyl ester (Pirodavir) | HY-1

Storage

Conservar a -20°C

Shipped In

Hielera + almohadillas de hielo

Descripción general Specifications Propiedades del producto Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Calculadoras de soluciones Reseñas

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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Conservar a -20°C Ships Hielera + almohadillas de hielo 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.

Descripción general

Pirodavir (R 77975) es el prototipo de una nueva clase de compuestos antipicornavirus de amplio espectro; potente inhibidor de la unión a la cápside del rinovirus humano (HRV).

Specifications

Sinónimos

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Descripción: Valor IC50: El pirodavir inhibe el 80 por ciento de los virus a 0, 064 microgramos/ml(EC80)[2]. El pirodavir fue uno de los compuestos de unión a la cápside más prometedores en mostrar eficacia en ensayos clínicos en humanos p

Condiciones de almacenamiento de almacenamiento

Conservar a -20°C

Enviado en

Hielera + almohadillas de hielo

Tipo de acción

DISRUPTING AGENT

Mecanismo de acción

VP1 capsid protein disrupting agent

Pureza

≥98%

Propiedades del producto

ALogP	3.7

Nombres e identificadores

Pubchem Sid	504754614
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504754614
Sonrisas canónicas	CCOC(=O)C1=CC=C(C=C1)OCCC2CCN(CC2)C3=NN=C(C=C3)C
IUPAC Name	ethyl 4-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]benzoate
InChIKey	KCHIOGFOPPOUJC-UHFFFAOYSA-N
INCHI	1S/C21H27N3O3/c1-3-26-21(25)18-5-7-19(8-6-18)27-15-12-17-10-13-24(14-11-17)20-9-4-16(2)22-23-20/h4-9,17H,3,10-15H2,1-2H3
Isómeros SMILES	CCOC(=O)C1=CC=C(C=C1)OCCC2CCN(CC2)C3=NN=C(C=C3)C
Peso molecular	369.46
Reaxy-Rn	8162239
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8162239&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 Benzenoids
  - Clase Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Clase	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Benzoic acid esters
Alternative Parents	Phenoxy compounds Phenol ethers Dialkylarylamines Benzoyl derivatives Aminopyridazines Alkyl aryl ethers Piperidines Imidolactams Heteroaromatic compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Benzoate ester - Phenoxy compound - Benzoyl - Phenol ether - Dialkylarylamine - Alkyl aryl ether - Aminopyridazine - Piperidine - Pyridazine - Imidolactam - Heteroaromatic compound - Carboxylic acid ester - Azacycle - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
External Descriptors	benzoate ester - pyridazinylpiperidine
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

Estructura 3D

Objetivos asociados (humanos)

MRC5 (9203 Activities)

Lot Number	Certificate Type	Fecha	Articulo
A2213386	Certificate of Analysis	Jul 14, 2025	P126501
A2213395	Certificate of Analysis	Jul 14, 2025	P126501
A2213396	Certificate of Analysis	Jul 14, 2025	P126501
K1513081	Certificate of Analysis	May 10, 2023	P126501

Solubilidad	25°C: DMSO 67 mg/mL; Water <1 mg/mL; Ethanol 7 mg/mL
Sensibilidad	Heat Sensitive
Punto de fusión (°C)	125 °C
Peso molecular	369.500 g/mol
XLogP3	3.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	8
Exact Mass	369.205 Da
Monoisotopic Mass	369.205 Da
Topological Polar Surface Area	64.599 Å²
Heavy Atom Count	27
Formal Charge	0
Complexity	446.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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