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PTEROLACTAM

PTEROLACTAM Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Email: support@targetmol.com
Products Intro: Product Name:Pterolactam
CAS:38072-88-7
Package:1 mg;5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
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Products Intro: Product Name:PterolactaM
CAS:38072-88-7
Remarks:C11881
Company Name: BioBioPha Co., Ltd.  
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Products Intro: Product Name:Pterolactam
CAS:38072-88-7
Purity:>97.0% Package:5mg Remarks:BBP00214
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
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Products Intro: CAS:38072-88-7
Purity:98% Package:5mg;10mg;20mg;50mg;100mg;200mg;500mg;1g
Company Name: Wuxi Zhongkun Biochemical Technology Co., Ltd.  
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Products Intro: Product Name:Pterolactam
CAS:38072-88-7
Purity:95%+ Package:根據(jù)客戶需求包裝
PTEROLACTAM Basic information
Product Name:PTEROLACTAM
Synonyms:PTEROLACTAM;(+)-5-Methoxypyrrolidin-2-one
CAS:38072-88-7
MF:C5H9NO2
MW:115.13
EINECS:
Product Categories:
Mol File:38072-88-7.mol
PTEROLACTAM Structure
PTEROLACTAM Chemical Properties
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Oil
Safety Information
MSDS Information
PTEROLACTAM Usage And Synthesis
UsesPterolactam can be isolated from Chrysanthemum coronarium L. Pterolactam derivates serval analogues that Mannich bases of amide with antifungal activities and cytotoxicity[1][2].
DefinitionChEBI: Pterolactam is a member of pyrrolidin-2-ones.
References[1] Song MC, et al. Heterocyclic compounds from Chrysanthemum coronarium L. and their inhibitory activity on hACAT-1, hACAT-2, and LDL-oxidation. Arch Pharm Res. 2008 May;31(5):573-8. DOI:10.1007/s12272-001-1195-4
[2] Dascalu AE, et al. Design, synthesis and antifungal activity of pterolactam-inspired amide Mannich bases. Fitoterapia. 2020 Jun;143:104581. DOI:10.1016/j.fitote.2020.104581
PTEROLACTAM Preparation Products And Raw materials
Tag:PTEROLACTAM(38072-88-7) Related Product Information
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