V-9302 HCl

V-9302 HCl Suppliers list
Company Name: Dalian Meilun Biotech Co., Ltd.  
Tel: 0411-62910999 13889544652
Email: sales@meilune.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Shanghai Rechem science Co., Ltd.  
Tel: 021-31433387 15618786686
Email: sales@rechemscience.com
Company Name: Shanghai Yu Ben Biotechnology Co., Ltd.  
Tel: 021-61350663 15502154572
Email: 1639466865@qq.com
Company Name: Zhejiang Huida Biotech Co., LTD  
Tel: 0571-89903022 18679456698
Email: zilong@hizyme.com
V-9302 HCl Basic information
Product Name:V-9302 HCl
Synonyms:(S)-2-Amino-4-(bis(2-((3-methylbenzyl)oxy)benzyl)amino)butanoic acid hydrochloride
CAS:2416138-42-4
MF:C34H39ClN2O4
MW:575.15
EINECS:
Product Categories:
Mol File:2416138-42-4.mol
V-9302 HCl Structure
V-9302 HCl Chemical Properties
storage temp. Store at -20°C
solubility DMSO: 250 mg/mL (434.68 mM)
form Solid
color White to off-white
Safety Information
MSDS Information
V-9302 HCl Usage And Synthesis
UsesV-9302 hydrochloride is a competitive antagonist of transmembrane glutamine flux. V-9302 hydrochloride selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) not ASCT1. V-9302 hydrochloride inhibits ASCT2-mediated glutamine uptake (IC50=9.6 μM) in HEK-293 cells[1].
in vivo

V-9302 hydrochloride (75 mg/kg; i.p.; daily fo 21 days) prevents tumor growth in both HCT-116 and HT29 xenograft models[1].
The combination of CB-839 and V-9302 (30 mg/kg; i.p.; SNU398 and MHCC97H cells were grown as tumor xenografts in BALB/c nude mice; for 20 or 15 d, respectively) elicits a strong growth inhibition in both SNU398 and MHCC97H xenograft models, while single-drug treatment showed modest anti-tumor effects[2].
V-9302 (50 mg/kg ; i.p.; daily for 5 days) displays markedly reduced tumor growth[3].

Animal Model:6-week old, female athymic nude mice (bearing HCT-116 (KRASG13D) or HT29 (BRAFV600E) cell-line )[1]
Dosage:75 mg/kg
Administration:Intraperitoneally; daily fo 21 days
Result:Prevented tumor growth.
IC 50ASCT2
References[1] Schulte ML, et al. Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacyin preclinical models. Nat Med. 2018 Feb;24(2):194-202. DOI:10.1038/nm.4464
[2] Jin H, et al. A powerful drug combination strategy targeting glutamine addiction for the treatment of human liver cancer. Elife. 2020;9:e56749. Published 2020 Oct 5. DOI:10.7554/eLife.56749
[3] Edwards DN, et al. Selective glutamine metabolism inhibition in tumor cells improves antitumor T lymphocyte activity in triple-negative breast cancer. J Clin Invest. 2021;131(4):e140100. DOI:10.1172/JCI140100
V-9302 HCl Preparation Products And Raw materials
Tag:V-9302 HCl(2416138-42-4) Related Product Information
2-Piperidinecarboxylic acid, 1-[[2,6-dimethoxy-4-[(2-methyl[1,1'-biphenyl]-3-yl)methoxy]phenyl]methyl]-, (2S)- V-9302 (hydrochloride) V-9302 HCl 1-(2-Methoxy-benzyl)-piperidine-2-carboxylic acid V-9302 Anti-Aging Compound Library