GAMMA-SECRETASE INHIBITOR XII

GAMMA-SECRETASE INHIBITOR XII Suppliers list
Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
Email: sales@alchempharmtech.com
Products Intro: Product Name:Benzyl ((2S,3S)-3-methyl-1-(((S)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopentan-2-yl)carbamate
CAS:161710-10-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-38246
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Z-Ile-Leu-aldehyde;GSI-XII;γ-Secretase inhibitor XII;Z-IL-CHO
CAS:161710-10-7
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:Z-Ile-Leu-aldehyde
CAS:161710-10-7
Purity:NLT 98% Remarks:MC528781
Company Name: Nanjing TGpeptide
Tel: +86-13347807150 +86-13347807150
Email: support@tgpeptide.com
Products Intro: Product Name:Z-Ile-Leu-aldehyde
CAS:161710-10-7
Purity:0.95 Package:1mg;5mg;10mg;50mg;100mg,1g
Company Name: Zhejiang Hangyu API Co., Ltd
Tel: +8617531972939
Email: anna@api-made.com
Products Intro: Product Name:Z-Ile-Leu-aldehyde
CAS:161710-10-7
Purity:99% Package:1g;25g;5KG;25KG
GAMMA-SECRETASE INHIBITOR XII Basic information
Product Name:GAMMA-SECRETASE INHIBITOR XII
Synonyms:Z-ILE-LEU-ALDEHYDE;Z-IL-CHO;GAMMA-SECRETASE INHIBITOR XII;Carbamic acid, N-[(1S,2S)-1-[[[(1S)-1-formyl-3-methylbutyl]amino]carbonyl]-2-methylbutyl]-, phenylmethyl ester;Benzyl ((2S,3S)-3-methyl-1-(((S)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopentan-2-yl)carbamate;Z-IL-CHO;GSI-XII;Γ-SECRETASE INHIBITOR XII;Z-ILE-LEU-ALDEHYDE(Z-IL-CHO; GSI-XII);Z-Ile-Leu-aldehyde(Z-IL-CHO
CAS:161710-10-7
MF:C20H30N2O4
MW:362.46
EINECS:
Product Categories:
Mol File:161710-10-7.mol
GAMMA-SECRETASE INHIBITOR XII Structure
GAMMA-SECRETASE INHIBITOR XII Chemical Properties
Boiling point 545.6±45.0 °C(Predicted)
density 1.074±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility insoluble in EtOH; insoluble in H2O; ≥10.8 mg/mL in DMSO
form solid
pka11.14±0.46(Predicted)
Safety Information
MSDS Information
GAMMA-SECRETASE INHIBITOR XII Usage And Synthesis
Biological Activityz-ile-leu-aldehyde (gamma-secretase inhibitor xii /gsi xii, z-il-cho) is a potent gamma-secretase inhibitor and notch signaling inhibitor.notch signaling impinges on many cellular processes, including cell proliferation, differentiation, apoptosis, and maintenance of stem cells. it is also involved in many developmental systems, including neurogenesis, angiogenesis, hematopoiesis, and myogenesis. deregulation of notch signaling leads to developmental syndromes and cancer [3]. in order to transmit a signal, notch receptors undergo a series of proteolytic cleavages after binding their cognate ligands of the delta-like and jagged family. γ-secretase is a large protease complex that cleaves the membrane-bound form of notch and releases the intracellular domain of the notch receptor. this step in notch signaling is pivotal in the activation of this signaling cascade [1] [2].ex vivo: a model of 3d culture of human breast cancer tissues was developed to study a series of 30 consecutive primary tumors from patients with untreated breast cancer for their sensitivity to the notch inhibitor gsi xii (15 μm). the results indicated that 24 tumors are sensitive to apoptosis induction by gsixii.
in vitrogsi xii (10~15 μm) blocked the notch signaling, reduced cell viability and induced apoptosis in mopc315.bm murine multiple myeloma cells in vitro. gsi xii (10 μm) impaired murine osteoclast differentiation of receptor activator of nf-κb ligand (rankl)-stimulated raw264.7 murine monocyte/macrophage cell line [1]. gsi xii (8 μm ~ 15 μm) potently triggered an apoptotic response through inhibition of notch activity in the breast cancer cells. gsi xii also targets mammary cancer stem-like cells because it dramatically prevented in vitro mammosphere formation [3].
in vivonotch inhibition through gsi xii (intraperitoneal injection, 10 mg/kg) reduced myeloma-specific paraprotein levels, bone loss and diminished osteolytic lesions in the mopc315.bm mice model[1]. notch inhibition using gsi xii (intraperitoneal injection, 5 mg/kg) blocked embryonal rhabdomyosarcoma tumorigenesis in mice[2].
references[1]. schwarzer r, nickel n, godau j, et al. notch pathway inhibition controls myeloma bone disease in the murine mopc315. bm model[j]. blood cancer journal, 2014, 4(6): e217.
[2]. belyea b c, naini s, bentley r c, et al. inhibition of the notch-hey1 axis blocks embryonal rhabdomyosarcoma tumorigenesis[j]. clinical cancer research, 2011, 17(23): 7324-7336.
[3]. séveno c, loussouarn d, bréchet s, et al. γ-secretase inhibition promotes cell death, noxa upregulation, and sensitization to bh3 mimetic abt-737 in human breast cancer cells[j]. breast cancer research, 2012, 14(3): r96.
GAMMA-SECRETASE INHIBITOR XII Preparation Products And Raw materials
Tag:GAMMA-SECRETASE INHIBITOR XII(161710-10-7) Related Product Information
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