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

COA

Grade & Purity:

≥99%

Cas Number: 1041434-82-5
Molecular Weight: 382.45
PubChem CID: 11954371
PubChem SID: 488197803

In stock

Item Number

P129200

Grouped product items
SKU	Size	Availability	Price
P129200-10mg	10mg	3	$317.90
P129200-100mg	100mg	3	$2,862.90
P129200-250mg	250mg	2	$6,439.90
P129200-1g	1g	1	$23,182.90
P129200-5g	5g	5	$104,319.90
P129200-25g	25g	1	$469,439.90

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Anti-infection (2803) Influenza Virus (253) Virus (1811)

Basic Description

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
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	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
Storage Temp	Protected from light,Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Action Type	INHIBITOR
Mechanism of action	Neuraminidase inhibitor
Product Description	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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Gamma amino acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives
Direct Parent	Gamma 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 Framework	Aliphatic 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
Description	This 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
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

Associated Targets(Human)

HEK293 (82097 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Staphylococcus aureus (210822 Activities)

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Acinetobacter baumannii (41033 Activities)

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Escherichia coli (133304 Activities)

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Cryptococcus neoformans (21258 Activities)

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Candida albicans (78123 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488197803
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488197803
IUPAC Name	(1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethylbutyl]-4-(diaminomethylideneamino)-2-hydroxycyclopentane-1-carboxylic acid;trihydrate
INCHI	InChI=1S/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
InChIKey	RFUCJKFZFXNIGB-ZBBHRWOZSA-N
Smiles	CCC(CC)C(C1C(CC(C1O)C(=O)O)N=C(N)N)NC(=O)C.O.O.O
Isomeric 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
Molecular Weight	382.45
Reaxy-Rn	30800735
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30800735&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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14 results found

Lot Number	Certificate Type	Date	Item
E2316041	Certificate of Analysis	Feb 07, 2025	P129200
E2316038	Certificate of Analysis	Feb 07, 2025	P129200
E2316045	Certificate of Analysis	Feb 07, 2025	P129200
E2316046	Certificate of Analysis	Feb 07, 2025	P129200
E2316043	Certificate of Analysis	Feb 07, 2025	P129200
E2316039	Certificate of Analysis	Feb 07, 2025	P129200
D2314315	Certificate of Analysis	Jan 14, 2025	P129200
D2314410	Certificate of Analysis	Jan 14, 2025	P129200
D2314327	Certificate of Analysis	Jan 14, 2025	P129200
D2314411	Certificate of Analysis	Jan 14, 2025	P129200
D23131168	Certificate of Analysis	Jan 14, 2025	P129200
C2306530	Certificate of Analysis	Mar 15, 2023	P129200
D2314409	Certificate of Analysis	Feb 24, 2023	P129200
F1511082	Certificate of Analysis	Jan 20, 2023	P129200

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Chemical and Physical Properties

Solubility	DMSO 0.2 mg/mL Water <1 mg/mL Ethanol <1 mg/mL
Sensitivity	Light & Air sensitive
Molecular Weight	382.450 g/mol
XLogP3
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	7
Exact Mass	382.243 Da
Monoisotopic Mass	382.243 Da
Topological Polar Surface Area	154.000 Å²
Heavy Atom Count	26
Formal Charge	0
Complexity	460.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
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	4

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

Basic Description

Taxonomic Classification

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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Chemical and Physical Properties

Solution Calculators

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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