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TAK 599

CAS No.
400827-46-5
Chemical Name:
TAK 599
Synonyms
TAK 599;PPI 0903;Ceftaroline fosaMil;C22H22N8O8PS4. C2H3O2;Ceftaroline Fosamil Acetate;TAK-599 (ceftaroline fosamil);Ceftaroline fosamil acetate salt;Ceftaroline Fosamil Acetate Impurity;TAK-599; CEFTAROLINE FOSAMIL;TAK599; TAK 599;PPI-0903;PPI0903;PPI 0903;N-phosphono,PPI 0903,inhibit,TAK599,MRSA,TAK 599,PPI-0903,T-91825,Bacterial,Inhibitor,Antibiotic,infection,Ceftaroline fosamil,prodrug
CBNumber:
CB02628440
Molecular Formula:
C24H25N8O10PS4
Molecular Weight:
744.72
MDL Number:
MOL File:
400827-46-5.mol
MSDS File:
SDS
Last updated:2023-05-21 10:59:17

TAK 599 Properties

storage temp. Store at -20°C
solubility DMSO : 30 mg/mL (40.28 mM; Need ultrasonic and warming)
form Powder
FDA UNII EZ9W6O5S09
ATC code J01DI02

Pharmacokinetic data

Protein binding 20%
Excreted unchanged in urine 88%
Volume of distribution 20.3 Litres
Biological half-life 2.5 / Increased

SAFETY

Risk and Safety Statements

TAK 599 price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 23696 TAK-599 ≥98% 400827-46-5 1mg $62 2024-03-01 Buy
Cayman Chemical 23696 TAK-599 ≥98% 400827-46-5 5mg $270 2024-03-01 Buy
Cayman Chemical 23696 TAK-599 ≥98% 400827-46-5 10mg $477 2024-03-01 Buy
ChemScene CS-2823 Ceftarolinefosamil 99.81% 400827-46-5 50mg $1450 2021-12-16 Buy
ChemScene CS-2823 Ceftarolinefosamil 99.81% 400827-46-5 100mg $2100 2021-12-16 Buy
Product number Packaging Price Buy
23696 1mg $62 Buy
23696 5mg $270 Buy
23696 10mg $477 Buy
CS-2823 50mg $1450 Buy
CS-2823 100mg $2100 Buy

TAK 599 Chemical Properties,Uses,Production

Description

Ceftaroline fosamil, also referred to as TAK-599, is a cephalosporin antibacterial agent that was approved in the United States in October 2010 for the IV treatment of acute bacterial skin and skin structure infections (ABSSSI) and community-acquired bacterial pneumonia (CABP). Ceftaroline fosamil is the water-soluble, N-phosphono prodrug of ceftaroline (T-91825), a broad-spectrum, bactericidal agent with potent activity against methicillin-resistant Staphylococcus aureus (MRSA) strains, multidrug resistant S. pneumonia, and common gram-negative organisms. Ceftaroline binds to PBP2a as well as other PBPs with high affinity and, as a result, retains potent activity. Ceftaroline exhibits activity against most gram-positive pathogens, including β-lactam-susceptible and -resistant S. aureus, vancomycin-resistant S. aureus, and resistant and susceptible forms of S. pneumoniae but has weak activity against Enterococcus sp. The gram-negative antibacterial activity of ceftaroline is limited mainly to respiratory pathogens such as Moraxella catarrhalis and Haemophilus influenzae.

Originator

Takeda (Japan)

Definition

ChEBI: An acetate salt obtained by reaction of ceftaroline fosamil with one equivalent of acetic acid. A prodrug for ceftaroline, used for the treatment of adults with acute bacterial skin and skin structure infections.

brand name

Teflaro

Synthesis

Reports from Takeda describe a process preparation of ceftaroline fosamil in 100 g scale which relies upon the assembly and union of fragments 112 and 114. The synthesis of fragment 112 began from commercially available benzhydryl 7b-[(phenylacetyl)amino]-3-hydroxy-3-cephem-4- carboxylate (106). The hydroxyl group within cephem 106 was reacted with methanesulfonyl chloride to produce mesylate 107 in 94% yield. The condensation of mesylate 107 with 4-(pyridin- 4-yl)thiazole-2-thiol 108 under the base condition of sodium methoxide gave compound 109 in 78% yield. Pyridinium salt 110 arose in quantitative yield upon subjection of 109 to iodomethane. Sequential deprotections of the amino group with phosphorous pentachloride and ester group with concentrated HCl afforded the dihydrochloride salt 112 in good yield.
Synthesis_400827-46-5
image.png

Acyl halide fragment 114 was prepared from commercially available (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetic acid (113) in 60% yield by dichlorophosphorylation of the amino group and concomitant acid chloride formation. Acid chloride 114 was then reacted with dihydrochloride salt 112 in the presence of sodium acetate to give N-phosphono cephem 115 in 77% yield. The crystallization of 115 in an aqueous acetic acid solution gave rise to the stable acetic acid solvate ceftaroline fosamil acetate (IX).

Drug interactions

Potentially hazardous interactions with other drugs
Anticoagulants: effects of coumarins may be enhanced.

Metabolism

Ceftaroline fosamil (prodrug) is converted into the active ceftaroline in plasma by phosphatase enzymes. Hydrolysis of the beta-lactam ring of ceftaroline occurs to form the microbiologically inactive, open-ring metabolite, ceftaroline M-1.
Ceftaroline is mainly eliminated by the kidneys. Renal clearance is approximately equal, or slightly lower than the glomerular filtration rate in the kidney, and in vitro transporter studies indicate that active secretion does not contribute to the renal elimination of ceftaroline.

TAK 599 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 75)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Wuhan Fortuna Chemical Co., Ltd
+86-27-59207850 +86-13986145403 info@fortunachem.com China 5985 58
changzhou huayang technology co., ltd
+8615250961469 2571773637@qq.com China 9821 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Shandong Zhishang New Material Co., Ltd.
+8617653113209 sales002@sdzschem.com China 3050 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58

View Lastest Price from TAK 599 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ceftaroline fosamil acetate pictures 2023-01-13 Ceftaroline fosamil acetate
400827-46-5
US $0.00 / G 1G 98%min 30kg/month WUHAN FORTUNA CHEMICAL CO., LTD
TAK 599 pictures 2019-07-06 TAK 599
400827-46-5
US $7.00 / kg 1kg 99% 100kg Career Henan Chemical Co
  • TAK 599 pictures
  • TAK 599
    400827-46-5
  • US $7.00 / kg
  • 99%
  • Career Henan Chemical Co
TAK 599 Ceftaroline fosaMil PPI 0903 TAK-599 (ceftaroline fosamil) Ceftaroline Fosamil Acetate C22H22N8O8PS4. C2H3O2 TAK-599; CEFTAROLINE FOSAMIL;TAK599; TAK 599;PPI-0903;PPI0903;PPI 0903 Ceftaroline fosamil acetate salt 4-(2-(((6R,7R)-2-Carboxy-7-((Z)-2-(ethoxyimino)-2-(5-(phosphonoamino)-1,2,4-thiadiazol-3-yl)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)thio)thiazol-4-yl)-1-methylpyridin-1-ium acetate Ceftaroline fosamilQ: What is Ceftaroline fosamil Q: What is the CAS Number of Ceftaroline fosamil Q: What is the storage condition of Ceftaroline fosamil N-phosphono,PPI 0903,inhibit,TAK599,MRSA,TAK 599,PPI-0903,T-91825,Bacterial,Inhibitor,Antibiotic,infection,Ceftaroline fosamil,prodrug Ceftaroline Fosamil Acetate Impurity 400827-46-5 C24H25N8O10PS4