Tigecycline (Mesylate)

Tigecycline (Mesylate) Suppliers list
Company Name: LETOPHARM LIMITED  
Tel: +86-21-5821 5861
Email: sales@letopharm.com
Company Name: SPIRO PHARMA  
Tel:
Email: eric_feng1954@126.com
Company Name: Musechem  
Tel: +1-800-259-7612
Email: info@musechem.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Tigecycline (Mesylate) Basic information
Product Name:Tigecycline (Mesylate)
Synonyms:Tigecycline (Mesylate)
CAS:1135871-27-0
MF:C29H39N5O8.CH4O3S
MW:681.76
EINECS:
Product Categories:
Mol File:1135871-27-0.mol
Tigecycline (Mesylate) Structure
Tigecycline (Mesylate) Chemical Properties
storage temp. Store at -20°C
solubility Soluble in DMSO
form Powder
Safety Information
MSDS Information
Tigecycline (Mesylate) Usage And Synthesis
UsesTigecycline mesylate (GAR-936 mesylate) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL[1]. MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively[2].
in vivo

Tigecycline (50 mg/kg; intraperitoneal injection; twice a day; for 11 days) reduces tumor volume and weight in NOD/SCID mice[1].
The peak plasma concentration (Cmax), the terminal half-life (t1/2), area under the plasma concentration-time curve (AUC), clearance (CL) and volume of distribution (Vz) are 22.8μg/mL, 108.9 min, 1912.2min*μg/mL, 26.1 mL/min/kg, 4109.4 mL/kg for Tigecycline in saline, respectively. The peak plasma concentration (Cmax), the terminal half-life (t1/2), area under the plasma concentration-time curve (AUC), clearance (CL) and volume of distribution (Vz) are15.7μg/mL, 110.3 min, 2036.5 min*μg/mL, 24.6 mL/min/kg, 3906.2 mL/kg for Tigecycline in formulation (60 mg/mL pyruvate, 3 mg/mL ascorbic acid, pH 7 in saline) , respectively[1].

Animal Model:NOD/SCID mice with OCI-AML2 acute myeloid leukemia (AML) xenograft model[1]
Dosage:50 mg/kg
Administration:Intraperitoneal injection; twice a day; for 11 days
Result:Reduced tumor volume and weight.
Animal Model:NOD/SCID mice[1]
Dosage:50 mg/kg
Administration:Intraperitoneal injection; 360 minutes
Result:The peak plasma concentration (Cmax), the terminal half-life (t1/2), area under the plasma concentration-time curve (AUC), clearance (CL) and volume of distribution (Vz) are 22.8 μg/mL, 108.9 min, 1912.2 min*μg/mL, 26.1 mL/min/kg, 4109.4 mL/kg, respectively.
References[1] Jitkova Y, et al. A novel formulation of tigecycline has enhanced stability and sustained antibacterial and antileukemic activity. PLoS One. 2014 May 28;9(5):e95281. DOI:10.1371/journal.pone.0095281
[2] Falagas ME, et al. Activity of TP-6076 against carbapenem-resistant Acinetobacter baumannii isolates collected from inpatients in Greek hospitals. Int J Antimicrob Agents. 2018 Aug;52(2):269-271. DOI:10.1016/j.ijantimicag.2018.03.009
Tigecycline (Mesylate) Preparation Products And Raw materials
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