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Peramivir

CAS No.
330600-85-6
Chemical Name:
Peramivir
Synonyms
Bcx-1812;Rapiacta;PeraMiviv;Peramivir;Aids114230;Rwj-270201;Aids-114230;Peramivir Monomer;Peramivir(BCX-1812);Paramivir waterless
CBNumber:
CB41457720
Molecular Formula:
C15H28N4O4
Molecular Weight:
328.41
MDL Number:
MFCD09837902
MOL File:
330600-85-6.mol
MSDS File:
SDS
Last updated:2023-07-13 17:52:38

Peramivir Properties

Melting point 170 - 172°C (dec.)
Density 1.39
storage temp. 2-8°C
solubility Methanol (Slightly, Heated), Water (Slightly)
pka 4.08±0.70(Predicted)
form Solid
color White to Off-White
FDA UNII 9ZS94HQO3B
ATC code J05AH03

SAFETY

Risk and Safety Statements

Peramivir price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 23765 Peramivir ≥98% 330600-85-6 1mg $49 2024-03-01 Buy
Cayman Chemical 23765 Peramivir ≥98% 330600-85-6 5mg $202 2024-03-01 Buy
Cayman Chemical 23765 Peramivir ≥98% 330600-85-6 10mg $380 2024-03-01 Buy
Cayman Chemical 23765 Peramivir ≥98% 330600-85-6 25mg $830 2024-03-01 Buy
TRC P285500 Peramivir 330600-85-6 10mg $1455 2021-12-16 Buy
Product number Packaging Price Buy
23765 1mg $49 Buy
23765 5mg $202 Buy
23765 10mg $380 Buy
23765 25mg $830 Buy
P285500 10mg $1455 Buy

Peramivir Chemical Properties,Uses,Production

Description

Peramivir is a neuraminidase (NA) inhibitor that was approved in Japan in 2010 for treatment of patients with influenza. It is the only NA inhibitor available for IV use and is the first of two NA inhibitors approved in 2010, the second being the inhaled drug laninamivir octanoate . Peramivir is the only NA inhibitor approved for IV use,which gives it a unique place in influenza treatment for seriously ill patients. Peramivir was discovered using structure-based drug design and is synthesized in six steps from Boc-protected methyl (1S,4R)-4-amino-cyclopent-2-enecarboxylate, which is prepared from 2-azabicyclo[2.2.1]hept-5-en-3-one. Cycloaddition of the cyclopentene olefin with a nitrile oxide provided an intermediate fused cyclopentane-dihydroisoxazole. Hydrogenolysis and acetylation set up a fully functionalized cyclopentane with all four stereocenters established. Deprotection of the amine and acid groups was followed by installation of the guanidine moiety to provide peramivir. Like zanamivir and oseltamivir, peramivir is a potent inhibitor of influenza virus A and B NA [strain A(H1N1) IC50= 0.34 nM; strain A(H3N2) IC50= 0.60 nM; strain B IC50= 1.36 nM]. However, peramivir is less potent against oseltamivirresistant viruses that have the H275Y NA mutation. These viruses remain sensitive to zanamivir. Peramivir is active against influenza A and B viruses and has a lowenzymatic off-rate, suggesting that it could inhibitNAactivity for a prolonged period and allow lower frequency of dosing. Peramivir has proven efficacious in preclinical animal models of influenza infection.

Description

Peramivir is an inhibitor of influenza neuraminidase (IC50s = 0.09 and 11 nM for influenza A and B neuraminidases, respectively). It is selective for influenza neuraminidase over bacterial, mammalian, and other viral neuraminidases (IC50s = >300 μM). Peramivir inhibits neuraminidase activity in H1N1, H2N2, H3N2, and H6N2 influenza strains (IC50s = 0.09-1.1 nM) and reduces lysis of MDCK cells infected with influenza (EC50s = <0.01-21 nM). Pretreatment with peramivir (10-100 mg/kg) protects mice against lethal influenza infections. It also increases survival in ferrets infected intranasally with avian influenza type A H5N1 when injected intramuscularly after infection. Formulations containing peramivir have been used to treat influenza.

Chemical Properties

White to Off-White Solid

Originator

BioCryst Pharmaceuticals Inc. (United States)

Uses

A new antiviral agent for influenza treatment; it can be used as neuraminidase inhibitor for treating human and avian influenza.

Uses

Peramivir is a new antiviral agent for influenza treatment; it can be used as neuraminidase inhibitor for treating human and avian influenza

Definition

Peramivir is a member of the class of guanidines that is used (as its trihydrate) for the treatment of acute uncomplicated influenza in patients 18 years and older who have been symptomatic for no more than two days.

brand name

Rapiacta, PeramiFlu

Synthesis

Several syntheses of this drug have been reported and the improved route disclosed in a recent patent is described in the scheme. Ring opening of commercially available (?à)-2- azabicyclo[2.2.1]hept-5-en-3-one (117) with methanolic HCl followed by classical resolution with Ltartaric acid gave the (1S,4R)-methyl ester 118 in 85% yield. Protection of 118 with Boc anhydride and TEA in CH2Cl2 afforded carbamate 119 in 90% yield. Alkene 119 was then subject to nitrone dipolar cycloaddition conditions involving 2-ethyl-N-hydroxybutanimidoyl chloride 120 and triethylamine, followed by the basic workup and then treatment with methanolic HCl, ultimately resulting in dihydroisoxazole 121. Interestingly, the nitrone generated from 120 approached alkene 119 from the less hindered face and proceeded with remarkable regioselectivity to provide azacycle 121 in 76% yield for the three step sequence. Treatment of 121 with 1.5 eq. lithium aluminum hydride resulted in rupture of the N-O bond within this system, which afforded the amino alcohol 122 in 81% yield. It should be noted that neither the Boc group or the methyl ester were reduced under these reaction conditions. Then, a one-pot three step sequence involving acetylation of the amino group, removal of the Boc group, and hydrolysis of the carboxylic ester followed by guanylation with pyrazolecarboxamidine hydrochloride (123) provided peramivir (X) in 82% yield over the final four steps.

Synthesis_330600-85-6

Peramivir Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 108)Suppliers
Supplier Tel Email Country ProdList Advantage
PNP Biotech Co. Ltd
+8618516098983 sales@pnpbiotech.com China 1001 58
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15928 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
XI'AN TIANGUANGYUAN BIOTECH CO., LTD.
+86-029-86333380 18829239519 sales06@tgybio.com China 961 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58

Related articles

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  • Peramivir (trade name Rapivab) is an antiviral drug developed by BioCryst Pharmaceuticals for the treatment of influenza.
  • Apr 11,2022

View Lastest Price from Peramivir manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
peramivir pictures 2024-03-28 peramivir
330600-85-6
US $0.00 / kg 25kg 98% Inquiry PNP Biotech Co. Ltd
Peramivir pictures 2023-06-26 Peramivir
330600-85-6
US $200.00 / kg 1kg 99% 1000kg/Month Hebei Mingeng Biotechnology Co., Ltd
(1S,2R,3R,4R)-3-(1-acetamido-2-ethyl-butyl)-4-(diaminomethylideneamino)-2-hydroxy-cyclopentane-1-carboxylic acid pictures 2019-07-06 (1S,2R,3R,4R)-3-(1-acetamido-2-ethyl-butyl)-4-(diaminomethylideneamino)-2-hydroxy-cyclopentane-1-carboxylic acid
330600-85-6
US $1.00 / kg 1kg 95%-99% 100kg Career Henan Chemical Co
  • peramivir pictures
  • peramivir
    330600-85-6
  • US $0.00 / kg
  • 98%
  • PNP Biotech Co. Ltd
  • Peramivir pictures
  • Peramivir
    330600-85-6
  • US $200.00 / kg
  • 99%
  • Hebei Mingeng Biotechnology Co., Ltd

Peramivir Spectrum

330600-85-6(Peramivir)Related Search:

(1S,2S,3R,4R)-3-((S)-1-AcetaMido-2-ethylbutyl)-4-guanidino-2-hydroxycyclopentanecarboxylic acid (1S,2R,3R,4R)-3-(1-acetamido-2-ethyl-butyl)-4-(diaminomethylideneamino)-2-hydroxy-cyclopentane-1-carboxylic acid (1S,2S,3R,4R)-3-[(1S)-1-(Acetylamino)-2-ethylbutyl]-4-[(aminoiminomethyl)amino]-2-hydroxycyclopentanecarboxylic acid Aids114230 Aids-114230 Bcx-1812 Cyclopentanecarboxylic acid, 3-[(1S)-1-(acetylamino)-2-ethylbutyl]-4-[(aminoiminomethyl)amino]-2-hydroxy-, (1S,2S,3R,4R)- Rwj-270201 Peramivir(BCX-1812) PeraMivir(RWJ-270201,BCX-1812) PeraMiviv Rapiacta (1S,2R,3R,4R)-3-(1-acetaMido-2-ethyl-butyl)-4-(diaMinoMethylideneaMino)-2-hydroxy-cyclopentane-1-car Peramivir (229614-55-5) peramivir Peramivir (BCX-1812, RWJ-270201, S-021812) (1S,2R,3R,4R)-3-(1-acetamido-2-ethyl-butyl)-4-(diaminomethyl 330600-85-6 Paramivir waterless Peramivir Monomer 330600-85-6 C15H28N4O4 Amines Chiral Reagents Intermediates & Fine Chemicals Pharmaceuticals API