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GAMMA-SECRETASE INHIBITOR XII

Product Name
GAMMA-SECRETASE INHIBITOR XII
CAS No.
161710-10-7
Chemical Name
GAMMA-SECRETASE INHIBITOR XII
Synonyms
GSI-XII);Z-IL-CHO;Z-ILE-LEU-ALDEHYDE;γ-Secretase inhibitor XII;Z-Ile-Leu-aldehyde(Z-IL-CHO;GAMMA-SECRETASE INHIBITOR XII;γ-Secretase inhibitor XII (GSI-XII);Z-ILE-LEU-ALDEHYDE(Z-IL-CHO; GSI-XII);Z-IL-CHO;GSI-XII;Γ-SECRETASE INHIBITOR XII;Benzyl ((2S,3S)-3-methyl-1-(((S)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopentan-2-yl)carbamate
CBNumber
CB0336194
Molecular Formula
C20H30N2O4
Formula Weight
362.46
MOL File
161710-10-7.mol
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GAMMA-SECRETASE INHIBITOR XII Property

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
pka
11.14±0.46(Predicted)
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ApexBio Technology
Product number
B4908
Product name
Z-Ile-Leu-aldehyde
Packaging
5mg
Price
$333
Updated
2021/12/16
ApexBio Technology
Product number
B4908
Product name
Z-Ile-Leu-aldehyde
Packaging
10mM(in 1mL DMSO)
Price
$390
Updated
2021/12/16
ChemScene
Product number
CS-3642
Product name
Z-Ile-Leu-aldehyde
Purity
≥98.0%
Packaging
5mg
Price
$420
Updated
2021/12/16
ChemScene
Product number
CS-3642
Product name
Z-Ile-Leu-aldehyde
Purity
≥98.0%
Packaging
10mg
Price
$600
Updated
2021/12/16
Biorbyt Ltd
Product number
orb611572
Product name
Z-Ile-Leu-aldehyde
Packaging
100mg
Price
$1654.1
Updated
2021/12/16
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GAMMA-SECRETASE INHIBITOR XII Chemical Properties,Usage,Production

Biological Activity

z-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 vitro

gsi 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 vivo

notch 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

Raw materials

Preparation Products

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GAMMA-SECRETASE INHIBITOR XII Suppliers

Creative Peptides
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Musechem
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TargetMol Chemicals Inc.
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+1-781-999-5354 +1-00000000000
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Alchem Pharmtech,Inc.
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8485655694
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TargetMol Chemicals Inc.
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support@targetmol.com
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ApexBio Technology
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3B Scientific Corporation
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EMD Biosciences, Inc.
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MedChemExpress
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161710-10-7, GAMMA-SECRETASE INHIBITOR XIIRelated Search:


  • Z-ILE-LEU-ALDEHYDE
  • Z-IL-CHO
  • GAMMA-SECRETASE INHIBITOR XII
  • γ-Secretase inhibitor XII (GSI-XII)
  • GSI-XII)
  • Z-Ile-Leu-aldehyde(Z-IL-CHO
  • Z-ILE-LEU-ALDEHYDE(Z-IL-CHO; GSI-XII)
  • Z-IL-CHO;GSI-XII;Γ-SECRETASE INHIBITOR XII
  • Benzyl ((2S,3S)-3-methyl-1-(((S)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopentan-2-yl)carbamate
  • Carbamic acid, N-[(1S,2S)-1-[[[(1S)-1-formyl-3-methylbutyl]amino]carbonyl]-2-methylbutyl]-, phenylmethyl ester
  • γ-Secretase inhibitor XII
  • 161710-10-7