U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C17H31ClN2O5S.ClH.H2O
Molecular Weight 465.433
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIRLIMYCIN HYDROCHLORIDE

SMILES

O.Cl.[H][C@@](NC(=O)[C@@H]1C[C@H](CC)CCN1)([C@H](C)Cl)[C@@]2([H])O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O

InChI

InChIKey=CHAZSEMQYSZBFN-RWMVMHIMSA-N
InChI=1S/C17H31ClN2O5S.ClH.H2O/c1-4-9-5-6-19-10(7-9)16(24)20-11(8(2)18)15-13(22)12(21)14(23)17(25-15)26-3;;/h8-15,17,19,21-23H,4-7H2,1-3H3,(H,20,24);1H;1H2/t8-,9+,10-,11+,12-,13+,14+,15+,17+;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C17H31ClN2O5S
Molecular Weight 410.956
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Pirlimycin is an antibiotic which was approved in the US and Europe for the treatment of subclinical mastitis in lactating dairy cattle associated with common mastitis pathogens, mostly Gram-positive bacterias. The drug exerts its action by binding to the 50S ribosomal subunit, therefore hindering the aminoacyl-tRNA binding and inhibiting the peptidyltransferase reaction, which interferes with protein synthesis within the bacteria.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
PIRSUE

Approved Use

PIRSUE Sterile Solution (pirlimycin hydrochloride) is indicated for the treatment of clinical and subclinical mastitis in lactating dairy cattle associated with Staphylococcus species such as Staphylococcus aureus and Streptococcus species such as Streptococcus agalactiae, Streptococcus dysgalactiae, and Streptococcus uberis.

Launch Date

1993
PubMed

PubMed

TitleDatePubMed
In vitro activity of U-57930E against anaerobic bacteria and its comparison with clindamycin, ampicillin, carbenicillin and tetracycline.
1983 Jan
Susceptibility of bacteria to serum lysis or phagocytosis following growth in subinhibitory levels of lincosaminide or spectinomycin related antibiotics.
1986 Jul
Quantum mechanical studies of lincosamides.
2012 Jun
Effect of lactation therapy on Staphylococcus aureus transmission dynamics in two commercial dairy herds.
2013 Feb 11
Patents

Sample Use Guides

Infuse the contents of one syringe (1 syringe contains pirlimycin hydrochloride equivalent to 50 mg pirlimycin (5 mg/ml)) into each affected quarter by intramammary infusion. Repeat this treatment once, after a 24-hour interval.
Route of Administration: Other
In Vitro Use Guide
Subcultures (0.15 ml) from the clear wells inoculated onto blood agar plates were examined after 24 and 48 h of incubation with pirlimycin at 37C. MIC50 values were 0.5 ug/ml (Staphylococcus aureus, methicillin susceptible); 2 ug/ml (Staphylococcus aureus, methicillin resistant); 1 ug/ml (Staphylococcus sp.); 0.25 ug/ml (Streptococcus pyogenes); 0.5 ug/ml (Streptococcus agalactiae); 0.25 ug/ml (Streptococcus pneumoniae, penicillin susceptible); 0.5 ug/ml (Streptococcus viridans).
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:34:08 GMT 2023
Edited
by admin
on Fri Dec 15 16:34:08 GMT 2023
Record UNII
8S09O559AQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIRLIMYCIN HYDROCHLORIDE
GREEN BOOK   MART.   USAN  
USAN  
Official Name English
PIRLIMYCIN HYDROCHLORIDE [GREEN BOOK]
Common Name English
METHYL 7-CHLORO-6,7,8-TRIDEOXY-6-CIS-4-ETHYL-L-PIPECOLAMIDO)-1-THIO-L-THREO-.ALPHA.-D-GALACTO-OCTOPYRANOSIDE MONOHYDROCHLORIDE MONOHYDRATE
Common Name English
PIRLIMYCIN HCL
Common Name English
PIRLIMYCIN HYDROCHLORIDE [USAN]
Common Name English
PIRLIMYCIN HYDROCHLORIDE HYDRATE [JAN]
Common Name English
L-THREO-.ALPHA.-D-GALACTO-OCTOPYRANOSIDE, METHYL 7-CHLORO-6,7,8-TRIDEOXY-6-(((4-ETHYL-2-PIPERIDINYL)CARBONYL)AMINO)-1-THIO-, MONOHYDROCHLORIDE, MONOHYDRATE, (2S-CIS)-
Common Name English
U-57,930E
Code English
U-57930E
Code English
PIRLIMYCIN HYDROCHLORIDE MONOHYDRATE
Common Name English
PIRLIMYCIN HYDROCHLORIDE [MART.]
Common Name English
PIRLIMYCIN HYDROCHLORIDE HYDRATE
JAN  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C82922
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
Code System Code Type Description
PUBCHEM
20055247
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
SMS_ID
300000023794
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
FDA UNII
8S09O559AQ
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
NCI_THESAURUS
C73846
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
ChEMBL
CHEMBL1652611
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
DAILYMED
8S09O559AQ
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID40998679
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
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DRUG BANK
DBSALT001696
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
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WIKIPEDIA
Pirlimycin hydrochloride
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
RXCUI
1367291
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY RxNorm
CAS
77495-92-2
Created by admin on Fri Dec 15 16:34:08 GMT 2023 , Edited by admin on Fri Dec 15 16:34:08 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
PARENT -> SALT/SOLVATE
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ACTIVE MOIETY