Peramivir Trihydrate - ≥99% , Neuraminidase inhibitor, CAS No.1041434-82-5, Neuraminidase inhibitor

CAS: 1041434-82-5 Cat. No.: P129200 Formula: C15H28N4O4·3H2O Peso molecolare: 382.45
Disponibile su ordine
GRADE & PURITY ≥99%
Synonyms
PeramivirTrihydrate | Rapivab (TN) | BAICALEIN [USP-RS] | (1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethylbutyl]-4-(diaminomethylideneamino)-2-hydroxycyclopentane-1-carboxylic acid;trihydrate | s2716 | (1S,2S,3R,4R)-3-((1S)-1-acetamido-2-ethylbutyl)-4-((amino(im
Storage
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
★
Size
Germania (EU)
USA*
Price
Qty
10mg
P129200-10mg
—
3 Disponibile

10,33€

15,53€
Salva 5,21 € (33.52%)
100mg
P129200-100mg
—
3 Disponibile

16,40€

25,08€
Salva 8,68 € (34.60%)
250mg
P129200-250mg
—
2 Disponibile

21,61€

32,89€
Salva 11,28 € (34.30%)
1g
P129200-1g
—
1 Disponibile

45,90€

69,33€
Salva 23,43 € (33.79%)
5g
P129200-5g
—
5 Disponibile

207,30€

311,43€
Salva 104,13 € (33.44%)
25g
P129200-25g
—
1 Disponibile

644,64€

967,44€
Salva 322,80 € (33.37%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Peramivir Trihydrate is a trihydrate of the anti-infection agent peramivir (RWJ-270201,BCX-1812) which is a transition-state analogue and a potent, specific influenza viral neuraminidase inhibitor with an IC50 of median 0.09 nM.

Specifications

Sinonimi
PeramivirTrihydrate | Rapivab (TN) | BAICALEIN [USP-RS] | (1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethylbutyl]-4-(diaminomethylideneamino)-2-hydroxycyclopentane-1-carboxylic acid;trihydrate | s2716 | (1S,2S,3R,4R)-3-((1S)-1-acetamido-2-ethylbutyl)-4-((amino(im
Specifiche e purezza
≥99%
Meccanismi biochimici e fisiologici

Peramivir is an experimental antiviral drug developed by BioCryst Pharmaceuticals for the treatment of influenza. It has been authorized for the emergency use of treatment of certain hospitalized patients with known or suspected 2009 H1N1

Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C,Argon charged
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
INHIBITOR
Meccanismo d'azione
Neuraminidase inhibitor
Purezza
≥99%
Nomi e identificatori
Pubchem Sid488197803
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488197803
Sorrisi canoniciCCC(CC)C(C1C(CC(C1O)C(=O)O)N=C(N)N)NC(=O)C.O.O.O
IUPAC Name(1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethylbutyl]-4-(diaminomethylideneamino)-2-hydroxycyclopentane-1-carboxylic acid;trihydrate
InChIKeyRFUCJKFZFXNIGB-ZBBHRWOZSA-N
INCHI1S/C15H28N4O4.3H2O/c1-4-8(5-2)12(18-7(3)20)11-10(19-15(16)17)6-9(13(11)21)14(22)23;;;/h8-13,21H,4-6H2,1-3H3,(H,18,20)(H,22,23)(H4,16,17,19);3*1H2/t9-,10+,11+,12-,13+;;;/m0.../s1
Isomeri SMILES CCC(CC)[C@@H]([C@H]1[C@@H](C[C@@H]([C@H]1O)C(=O)O)N=C(N)N)NC(=O)C.O.O.O
Peso molecolare 382.45
Reaxy-Rn 30800735
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30800735&ln=

Documentazione

📋 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
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives
Direct ParentGamma amino acids and derivatives
Alternative Parents Beta hydroxy acids and derivatives  Cyclopentanols  Acetamides  Secondary carboxylic acid amides  Guanidines  Cyclic alcohols and derivatives  Propargyl-type 1,3-dipolar organic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Carboximidamides  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Gamma amino acid or derivatives - Beta-hydroxy acid - Cyclopentanol - Hydroxy acid - Cyclic alcohol - Acetamide - Carboxamide group - Guanidine - Secondary alcohol - Secondary carboxylic acid amide - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Carboximidamide - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aliphatic homomonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

16 results found

Lot NumberCertificate TypeDataOggetto
A2628089Certificate of AnalysisFeb 04, 2026 P129200
C2306530Certificate of AnalysisDec 10, 2024 P129200
F1511082Certificate of AnalysisOct 16, 2024 P129200
E2316038Certificate of AnalysisMar 24, 2023 P129200
E2316039Certificate of AnalysisMar 24, 2023 P129200
E2316041Certificate of AnalysisMar 24, 2023 P129200
E2316043Certificate of AnalysisMar 24, 2023 P129200
E2316045Certificate of AnalysisMar 24, 2023 P129200
E2316046Certificate of AnalysisMar 24, 2023 P129200
201408290012Certificate of AnalysisFeb 24, 2023 P129200
D23131168Certificate of AnalysisFeb 24, 2023 P129200
D2314315Certificate of AnalysisFeb 24, 2023 P129200
D2314327Certificate of AnalysisFeb 24, 2023 P129200
D2314409Certificate of AnalysisFeb 24, 2023 P129200
D2314410Certificate of AnalysisFeb 24, 2023 P129200
D2314411Certificate of AnalysisFeb 24, 2023 P129200

Show more ⌵

Proprietà chimiche e fisiche
SolubilitàDMSO 0.2 mg/mL Water <1 mg/mL Ethanol <1 mg/mL
SensibilitàLight & Air sensitive
Peso molecolare382.450 g/mol
XLogP3
Hydrogen Bond Donor Count8
Hydrogen Bond Acceptor Count8
Rotatable Bond Count7
Exact Mass382.243 Da
Monoisotopic Mass382.243 Da
Topological Polar Surface Area154.000 Ų
Heavy Atom Count26
Formal Charge0
Complexity460.000
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count4
Citations of This Product
Riferimenti
1. Zhongnan Hu, Hui Liu, Weihua Wu, Tayyab Ali, Adam Junka, Farukh S. Sharopov, Xuan Zou, Shisong Fang, Yanfang Sun.  (2026)  Artemisia Extracts Suppress H1N1 Influenza A Virus Infection by Targeting Viral HA/NA Proteins and Modulating the TLR4/MyD88/NF-κB Signaling Axis.  Pharmaceuticals,  19  (2): (275).  [PMID:41754817] [10.3390/ph19020275]
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

What are the CAS number, molecular formula and molecular weight?
The CAS Number is 1041434-82-5, the molecular formula is C15H28N4O4·3H2O, and the molecular weight is 382.45 g/mol. InChIKey RFUCJKFZFXNIGB-ZBBHRWOZSA-N.
What is the purity of this product?
This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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.