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RETAPAMULIN

CAS No.
224452-66-8
Chemical Name:
RETAPAMULIN
Synonyms
CS-329;Retamole;SB-275833;Rebapamulin;RETAPAMULIN;tetapaMulin;Rui he Maureen;RetapaMulin API;Retapamulin, >=98%;RetapaMulin (SB-275833)
CBNumber:
CB32455623
Molecular Formula:
C30H47NO4S
Molecular Weight:
517.76
MDL Number:
MFCD11045316
MOL File:
224452-66-8.mol
Last updated:2023-11-03 14:46:39

RETAPAMULIN Properties

Boiling point 594.9±50.0 °C(Predicted)
Density 1.16±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility insoluble in H2O; ≥114.8 mg/mL in EtOH; ≥16.15 mg/mL in DMSO
form solid
pka 14.65±0.70(Predicted)
InChIKey STZYTFJPGGDRJD-IFPFAXJDNA-N
CAS DataBase Reference 224452-66-8(CAS DataBase Reference)
FDA UNII 4MG6O8991R
ATC code D06AX13

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H412
Precautionary statements  P273-P501
NFPA 704
0
2 0

RETAPAMULIN price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21528 Retapamulin ≥99% 224452-66-8 1mg $62 2024-03-01 Buy
Cayman Chemical 21528 Retapamulin ≥99% 224452-66-8 5mg $270 2024-03-01 Buy
Cayman Chemical 21528 Retapamulin ≥99% 224452-66-8 10mg $477 2024-03-01 Buy
Cayman Chemical 21528 Retapamulin ≥99% 224452-66-8 25mg $1041 2024-03-01 Buy
Biorbyt Ltd orb146178 Retapamulin >99% 224452-66-8 1g $1802 2021-12-16 Buy
Product number Packaging Price Buy
21528 1mg $62 Buy
21528 5mg $270 Buy
21528 10mg $477 Buy
21528 25mg $1041 Buy
orb146178 1g $1802 Buy

RETAPAMULIN Chemical Properties,Uses,Production

Description

Antibacterial retapamulin is a derivative of the natural product pleuromutilin and was developed by Glaxo and approved in the US in 2007 for the treatment of skin infections. It has a unique mechanism of action, inhibiting bacterial protein synthesis by inhibiting the larger subunit of the ribosome, and thus has no cross resistance to other antibacterial agents. Pleuromutilin is a tricyclic diterpenoid that was first isolated in 1951 from the edible mushroom Pleurotus mutilus. The first semisynthetic analogs tiamulin and valnemulin, developed for veterinary use, have been shown to interact uniquely with bacterial ribosomes by high affinity binding to a site on the 50S subunit. Binding to this site interferes with ribosomal peptidyl transferase activity, blocks P-site interactions, and prevents the evolution of active 50S ribosomal subunits. Retapamulin, the first pleuromutilin approved for human use, behaves similarly to selectively inhibit bacterial protein synthesis. This novel mechanism of action has been implicated in the lack of in vitro target-specific cross-resistance with other classes of antibiotics.

Originator

GlaxoSmithKline (US)

Uses

A broad spectrum antibiotic with no cross resistance to existing classes

Uses

Retapamulin is a semi-synthetic pleuromutilin prepared by reacting pleuromutilin tosylate with tropine-3-thiol to give a more hydrophobic analogue with a tertiary amine. This enables formulation as a stable hydrochloride salt. Retapamulin is a broad spectrum antibiotic with no cross resistance to existing antibiotic classes, and is the first pleuromutilin approved for human use. Like all the pleuromutilins, retapamulin inhibits protein synthesis by binding to domain V of 23S rRNA.

Uses

Retapamulin is a topical antibiotic, which binds to both E. coli and S. aureus ribosomes with similar potencies with Kd of 3 nM

Uses

Retapamulin is a semi-synthetic pleuormutilin prepared by reacting pleuromutilin tosylate with tropine-3-thiol to give a more hydrophobic analogue with a tertiary amine. This enables formulation as a stable hydrochloride salt. Retapamulin is a broad spectrum antibiotic with no cross resistance to existing antibiotic classes, and is the first pleuromutilin approved for human use. Like all the pleuromutilins, retapamulin inhibits protein synthesis by binding to domain V of 23S rRNA.

Definition

ChEBI: Retapamulin is a carbotricyclic compound, a carboxylic ester and a cyclic ketone.

brand name

Altabax

Pharmaceutical Applications

A semisynthetic pleuromutilin formulated as a 1% ointment for topical use. It is active against staphylococci (MIC 0.12 mg/L), including methicillin-resistant strains, and against streptococci (MIC 0.03–0.25 mg/L), including Str. pyogenes and Str. pneumoniae. Most enterococci and Gramnegative bacilli are resistant. Propionibacteria are susceptible, suggesting that it might be useful in acne. Early indications suggest that resistance does not emerge readily, but experience with veterinary pleuromutilins indicates that chromosomal resistance may develop with extended use.
It is metabolized in the liver and rapidly excreted, precluding use in systemic infection. Systemic exposure is said to be low following topical application and it appears safe, but there are few data on absorption through broken and unbroken skin. Principal side effects noted include local irritation and occasional allergic reactions. Licensed use is presently restricted to the treatment of impetigo and uncomplicated skin infections. Possible value in methicillin-resistant Staph. aureus (MRSA) infection or carriage has not yet been established.

Side effects

The most frequent adverse event was application site irritation, but other side effects, occurring in o2% of patients, included headache, diarrhea, nausea, and nasopharyngitis. While there are no contraindications, it is recommended that pregnant women only use retapamulin when the potential benefits outweigh the potential risks since animal reproductive studies are not always predictive of human response. Likewise, nursing mothers are cautioned about the unknown possibility of retapamulin excretion in breast milk.

Synthesis

The synthesis of retapamulin begins with generation of the mesylate of pleuromutilin, isolated through fermentation of Clitopilus passeckerianus, followed by nucleophilic substitution with exo-8-methyl-8-azabicyclo[3.2.1]octan-3-thiol under basic conditions Shridhar Hegde and Michelle Schmidt (potassium-tert-butoxide in ethanol or tetrabutylammonium hydrogen sulfate in dichloromethane/water and sodium hydroxide at pH 12.5). The azabicyclic thiol derivative may be prepared via a Mitsunobu reaction between tropine and thioacetic acid.

References

[1] jones r n, fritsche t r, sader h s, et al. activity of retapamulin (sb-275833), a novel pleuromutilin, against selected resistant gram-positive cocci. antimicrobial agents and chemotherapy, 2006, 50(7): 2583-2586.
[2] rittenhouse s, biswas s, broskey j, et al. selection of retapamulin, a novel pleuromutilin for topical use. antimicrobial agents and chemotherapy, 2006, 50(11): 3882-3885.

848130-83-6
60924-38-1
224452-66-8
Synthesis of RETAPAMULIN from 8-Azabicyclo[3.2.1]octane-3-thiol, 8-Methyl-, (3-exo)- and 2-[(Methylsulfonyl)oxy]acetic acid (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyldecahydro-5-hydroxy-4,6,9,10-tetramethyl-1-oxo-3a,9-propano-3aH-cyclopentacycloocten-8-yl ester
Global( 220)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing Mediking Biopharm Co., Ltd
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ATK CHEMICAL COMPANY LIMITED
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BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58

View Lastest Price from RETAPAMULIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Retapamulin pictures 2023-11-03 Retapamulin
224452-66-8
US $0.00 / kg 1kg 99% 2 t Beijing Mediking Biopharm Co., Ltd
RETAPAMULIN pictures 2023-03-24 RETAPAMULIN
224452-66-8
US $60.00 / kg 1kg 98% 20 tons Hebei Duling International Trade Co. LTD
RETAPAMULIN pictures 2022-09-08 RETAPAMULIN
224452-66-8
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
  • Retapamulin pictures
  • Retapamulin
    224452-66-8
  • US $0.00 / kg
  • 99%
  • Beijing Mediking Biopharm Co., Ltd
  • RETAPAMULIN pictures
  • RETAPAMULIN
    224452-66-8
  • US $60.00 / kg
  • 98%
  • Hebei Duling International Trade Co. LTD
  • RETAPAMULIN pictures
  • RETAPAMULIN
    224452-66-8
  • US $0.00-0.00 / kg
  • 98%
  • Henan Aochuang Chemical Co.,Ltd.

RETAPAMULIN Spectrum

RETAPAMULIN RetapaMulin (SB-275833) (3aS,4R,5S,6S,8R,9R,9aR,10R)-2-(exo-8-Methyl-8-azabicyclo[3.2.1]octan-3-ylsulfanyl)acetic acid 5-hydroxy-4,6,9,10-tetraMethyl-1-oxo-6-vinylperhydro-3a,9-propanocyclopentacycloocten-8-yl ester RetapaMulin API tetapaMulin (1S,2R,3S,4S,6R,7R,8R,14R)-4-ethenyl-3-hydroxy-2,4,7,14-tetraMethyl-9-oxotricyclo[5.4.3.0^{1,8}]tetradecan-6-yl 2-{[(1R,3S,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl]sulfanyl}acetate Rebapamulin SB-275833 Acetic acid, 2-[[(3-exo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl]thio]-, (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyldecahydro-5-hydroxy-4,6,9,10-tetramethyl-1-oxo-3a,9-propano-3aH-cyclopentacycloocten-8-yl ester Retapamulin, >=98% Retamole CS-329 RetapamulinQ: What is Retapamulin Q: What is the CAS Number of Retapamulin Q: What is the storage condition of Retapamulin Q: What are the applications of Retapamulin Rui he Maureen 3-(2,5-dioxopyrrolidin-7-yl)propanoicacid N-Boc-piperidine-5-carbaldehyde Acetonitrile,2,3'-(nitrosoimino)bis- (3aR,4R,5R,7S,8S,9R,9aS,12R)-8-Hydroxy-4,7,9,12-tetramethyl-5-((3-(((3-exo)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)thio)prop-1-en-2-yl)oxy)-7-vinyloctahydro-4,9a-propanocyclopenta[8]annulen-3(3aH)-one 224452-66-8 924452-66-8 22452-66-8 C30H47NO4S C30H46NO4S Inhibitors API, Antibiotics