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Pirlimycin

Product Name
Pirlimycin
CAS No.
79548-73-5
Chemical Name
Pirlimycin
Synonyms
pyrimycin;Pirlimycin;Pirlimycina;Pirlimycine;Pirlimycinum;Pirlimycine [inn-french];Pirlimycinum [inn-latin];Pirlimycina [inn-spanish];Dexamethasone-4,6α,21,21-d;Methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-4-ethyl-2-piperidinyl]carbonyl]amino]-1-thio-L-threo-α-D-galacto-octopyranoside
CBNumber
CB7947410
Molecular Formula
C17H31ClN2O5S
Formula Weight
410.96
MOL File
79548-73-5.mol
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Pirlimycin Property

Boiling point:
643.9±55.0 °C(Predicted)
Density 
1.31
storage temp. 
Store at -20°C
solubility 
Soluble in ethanol;Soluble in methanol;Soluble in DMSO;Soluble in dimethyl formamide
form 
solid
pka
12.88±0.70(Predicted)
Stability:
Hygroscopic
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
20138
Product name
Pirlimycin
Purity
≥99%
Packaging
1mg
Price
$194
Updated
2024/03/01
Cayman Chemical
Product number
20138
Product name
Pirlimycin
Purity
≥99%
Packaging
5mg
Price
$773
Updated
2024/03/01
Usbiological
Product number
P4205-50
Product name
Pirlimycin
Packaging
500ul
Price
$393
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003875
Product name
PIRLIMYCIN
Purity
95.00%
Packaging
12KG
Price
$7069.76
Updated
2021/12/16
ApexBio Technology
Product number
C5005
Product name
Pirlimycin
Packaging
1mg
Price
$243
Updated
2021/12/16
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Pirlimycin Chemical Properties,Usage,Production

Uses

Pirlimycin is a semi-synthetic lincosamide prepared from clindamycin by hydrolysing the propyl N-methylproline and re-annealing a 4-ethylpipecolic acid. Pirlimycin is more hydrophobic than clindamycin and is more potent against a number of important pathogens. Like other members of the lincosamide family, pirlimycin is a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans. Pirlimycin acts by binding to the 23S ribosomal subunit, blocking protein synthesis. Pirlimycin has been less extensively researched than the older lincosamides.

Biological Activity

pirlimycin, a lincosamide antibiotic, is effective against gram-positive bacteria, including staphylococcus, bacteroides, streptococcus, and plasmodium. it functions via inhibiting protein synthesis in bacteria by inducing premature dissociation of the peptidyl-trna from the ribosome.

Veterinary Drugs and Treatments

Pirlimycin mastitis tubes are indicated for the treatment of clinical and subclinical mastitis caused by susceptible organisms in lactating dairy cattle.

in vitro

pirlimycin showed activity against helicobacter pylori with a minimal inhibitory concentration [mic] 50 of 4 μg/ml and an mic90 of 64 μg/ml [1].

in vivo

cows were treated with 50 mg of pirlimycin via two intramammary infusions per quarter at a 24-hour interval (2-day) for 2, 5, or 8 days. pirlimycin showed antibiotic therapy against environmental streptococcus spp and staphylococcus aureus intramammary individual and combined infections [1]. specifically, pirlimycin cured environmental streptococcus spp infections in 66.7% (14/21), 85% (17/20), 100% (14/14) in the 2-day group, 5-day group and 8-day group, respectively. s. aureus infections were cured by the treatment of pirlimycin in 13.3% (2/15), 31.3% (5/16), 83.3% (5/6) in the 2-day group, 5-day group and 8-day group, respectively. furthermore, s. aureus, s. dysgalactiae subsp dysgalactiae, and enterococcus spp intramammary infections were eliminated by the extended treatment of pirlimycin in 8-day group [2].

References

[1]. westblom, t., midkiff, b., & czinn, s. in vitro susceptibility ofhelicobacter pylori to trospectomycin, pirlimycin (u-57930e), mirincamycin (u-24729a) and n-demethyl clindamycin (u-26767a). european journal of clinical microbiology & infectious diseases. 1993; 12(7): 560-562.
[2]. b. e. gillespie, h. moorehead, p. lunn, h. h. dowlen, d. l. johnson, k. c. lamar, m. j. lewis, s. j. ivey, j. w. hallberg, s. t. chester, and s. p. oliver. efficacy of extended pirlimycin hydrochloride therapy for treatment of environmental streptococcus spp and staphylococcus aureus intramammary infections in lactating dairy cows. veterinary therapeutics. 2002; 3(4): 373-80.

Pirlimycin Preparation Products And Raw materials

Raw materials

Preparation Products

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Pirlimycin Suppliers

BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19741
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81

79548-73-5, PirlimycinRelated Search:


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  • Methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-4-ethyl-2-piperidinyl]carbonyl]amino]-1-thio-L-threo-alpha-D-galactooctopyranoside
  • Methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-4-ethyl-2-piperidinyl]carbonyl]amino]-1-thio-L-threo-α-D-galacto-octopyranoside
  • L-Threo-alpha-galacto-octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-((((2S,4R)-4-ethyl-2-piperidinyl)carbonyl)amino)-1-thio-
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  • Pirlimycine
  • Pirlimycine [inn-french]
  • Pirlimycinum
  • Pirlimycinum [inn-latin]
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  • L-threo-a-D-galacto-Octopyranoside, methyl7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-4-ethyl-2-piperidinyl]carbonyl]amino]-1-thio-
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  • 79548-73-5
  • C17H31ClN2O5S