Fosinopril Sodium - Moligand™,2mM in Water , Angiotensin-converting enzyme inhibitor, CAS No.88889-14-9, Angiotensin-converting enzyme inhibitor

CAS: 88889-14-9 Cat. No.: F426692 Peso molecular: 585.64 Número EC: 620-449-1 PubChem CID: 23681451
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 2mM in Water
Synonyms
Fosinopril, (1(S*(R*)),2 alpha,4 beta)-Isomer | Fosinopril sodium- Bio-X | A842989 | HY-P0018 | FOSINOPRIL SODIUM (USP MONOGRAPH) | (4S)-4-CYCLOHEXYL-1-((R)-((S)-1-HYDROXY-2-METHYLPROPOXY)(4-PHENYLBUTYL)PHOSPHINYL)ACETYL-L-PROLINE PROPIONATE (ESTER), SODI
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
F426692-1ml
1

58,90US$

69,90US$
Guardar 11,00 US$ (15.74%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™,2mM in Water Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

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

Descripción general

An angiotensin-converting enzyme inhibitor.

Specifications

Sinónimos
Fosinopril, (1(S*(R*)), 2 alpha, 4 beta)-Isomer | Fosinopril sodium- Bio-X | A842989 | HY-P0018 | FOSINOPRIL SODIUM (USP MONOGRAPH) | (4S)-4-CYCLOHEXYL-1-((R)-((S)-1-HYDROXY-2-METHYLPROPOXY)(4-PHENYLBUTYL)PHOSPHINYL)ACETYL-L-PROLINE PROPIONATE (ESTER), SODI
Especificaciones y pureza
Moligand™, 2mM in Water
Mecanismos bioquímicos y fisiológicos
Fosinopril sodium is an ACE(angiotensin-converting enzyme) inhibitor.Competitive ACE inhibitor. Prodrug of metabolite fosinoprilat. Shows antihypertensive effects in vivo. Orally active.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
INHIBITOR
Mecanismo de acción
Angiotensin-converting enzyme inhibitor
Nombres e identificadores
Sonrisas canónicasCCC(=O)OC(C(C)C)OP(=O)(CCCCC1=CC=CC=C1)CC(=O)N2CC(CC2C(=O)[O-])C3CCCCC3.[Na+]
IUPAC Namesodium;(2S,4S)-4-cyclohexyl-1-[2-[(2-methyl-1-propanoyloxypropoxy)-(4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylate
InChIKeyTVTJZMHAIQQZTL-HREVRLCXSA-M
INCHI1S/C30H46NO7P.Na/c1-4-28(33)37-30(22(2)3)38-39(36,18-12-11-15-23-13-7-5-8-14-23)21-27(32)31-20-25(19-26(31)29(34)35)24-16-9-6-10-17-24;/h5,7-8,13-14,22,24-26,30H,4,6,9-12,15-21H2,1-3H3,(H,34,35);/q;+1/p-1/t25-,26+,30?,39?;/m1./s1
Isómeros SMILES CCC(=O)OC(C(C)C)OP(=O)(CCCCC1=CC=CC=C1)CC(=O)N2C[C@@H](C[C@H]2C(=O)[O-])C3CCCCC3.[Na+]
WGK Alemania 3
PubChem CID 23681451
Peso molecular 585.64

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

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentProline and derivatives
Alternative Parents N-acyl-L-alpha-amino acids  Pyrrolidine carboxylic acids  N-acylpyrrolidines  Benzene and substituted derivatives  Dicarboxylic acids and derivatives  Tertiary carboxylic acid amides  Phosphinic acid esters  Carboxylic acid esters  Carboxylic acid salts  Carboxylic acids  Azacyclic compounds  Hydrocarbon derivatives  Organopnictogen compounds  Carbonyl compounds  Organonitrogen compounds  Organic sodium salts  Organic oxides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - Proline or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Dicarboxylic acid or derivatives - Benzenoid - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Carboxylic acid ester - Carboxylic acid salt - Phosphinic acid ester - Azacycle - Organic alkali metal salt - Carboxylic acid - Organoheterocyclic compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic sodium salt - Hydrocarbon derivative - Organooxygen compound - Organophosphorus compound - Organic salt - Carbonyl group - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as proline and derivatives. These are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors organic sodium salt
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular585.600 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count7
Rotatable Bond Count15
Exact Mass585.283 Da
Monoisotopic Mass585.283 Da
Topological Polar Surface Area113.000 Ų
Heavy Atom Count40
Formal Charge0
Complexity857.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View Moligand™ grade guide →

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.