ARM1

ARM1 Suppliers list
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com

ARM1 manufacturers

  • ARM1
  • ARM1 pictures
  • $43.00
  • 2026-08-08
  • CAS:68729-05-5
  • Purity: 99.36%
  • Supply Ability: 10g
ARM1 Basic information
Product Name:ARM1
Synonyms:ARM1;4-(4-Benzylphenyl)-1,3-thiazol-2-amine;ARM-1 (ARM1);2-Thiazolamine, 4-[4-(phenylmethyl)phenyl]-;Epoxide Hydrolase,ARM1,HCT-116 cells,Inhibitor,LTA4H,ARM-1,cytotoxic,positive control,Aminopeptidase,4BSA,inhibit,ARM 1;2-Thiazolamine, 4-[4-(phenylmethyl)phenyl]- , ARM1;ARM1, 10 mM in DMSO
CAS:68729-05-5
MF:C16H14N2S
MW:266.36
EINECS:
Product Categories:
Mol File:68729-05-5.mol
ARM1 Structure
ARM1 Chemical Properties
storage temp. Store at -20°C
solubility ≤1mg/ml in ethanol;10mg/ml in DMSO;15mg/ml in dimethyl formamide
form crystalline solid
color Off-white to light yellow
SMILESC1=CC=C(C=C1)CC2=CC=C(C=C2)C3=CSC(=N3)N
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
ARM1 Usage And Synthesis
DescriptionLeukotriene A4 (LTA4) hydrolase/aminopeptidase is a bifunctional zinc metalloenzyme that both catalyzes the synthesis of LTB4 from LTA4 and cleaves the chemotactic peptide Pro-Gly-Pro. ARM1 is a thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~0.5 μM) and conversion of LTA4 to LTB4 by purified LTA4 hydrolase (Ki = 2.3 μM). ARM1 does not significantly affect the hydrolysis of Pro-Gly-Pro by LTA4 hydrolase.
UsesLeukotriene A4 (LTA4) hydrolase/aminopeptidase is a bifunctional zinc metalloenzyme that both catalyzes the synthesis of LTB4 from LTA4 and cleaves the chemotactic peptide Pro-Gly-Pro. ARM1 is a thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~0.5 μM) and conversion of LTA4 to LTB4 by purified LTA4 hydrolase (Ki = 2.3 μM). ARM1 does not significantly affect the hydrolysis of Pro-Gly-Pro by LTA4 hydrolase.[Cayman Chemical]
references[1]. stsiapanava a, olsson u, wan m, et al. binding of pro-gly-pro at the active site of leukotriene a4 hydrolase/aminopeptidase and development of an epoxide hydrolase selective inhibitor. proc natl acad sci u s a. 2014 mar 18;111(11):4227-32.
[2]. haeggstrm jz. leukotriene a4 hydrolase/aminopeptidase, the gatekeeper of chemotactic leukotriene b4 biosynthesis. j biol chem. 2004 dec 3;279(49):50639-42.
[3]. snelgrove rj, jackson pl, hardison mt, et al. a critical role for lta4h in limiting chronic pulmonary neutrophilic inflammation. science. 2010 oct 1;330(6000):90-4.
ARM1 Preparation Products And Raw materials
Tag:ARM1(68729-05-5) Related Product Information
2-Thiazolamine, 4-[3-(4-pyridinyl)phenyl]- 2-Thiazolamine, 4-[3-(2-thiazolyl)phenyl]- 2-Thiazolamine, 4-[3-(2,6-dimethyl-4-pyridinyl)phenyl]- ARM1 4-(3-bromo-4-methylphenyl)-1,3-thiazol-2-amine 4-(6-tert-butyl-1,1-dimethyl-2,3-dihydroinden-4-yl)-1,3-thiazol-2-amine