ChemicalBook >> CAS DataBase List >>Terevalefim

Terevalefim

CAS No.
1070881-42-3
Chemical Name:
Terevalefim
Synonyms
Terevalefim;Terevalefim(ANG-3777);(E)-3-(2-(thiophen-2-yl)vinyl)-1H-pyrazole;1H-Pyrazole, 3-[(1E)-2-(2-thienyl)ethenyl]-;3-[(E)-2-(thiophen-2-yl)ethenyl]-2H-pyrazole;ANG-3777,Terevalefim,injury,acute,inhibit,ANG 3777,AKI,kidney,ANG3777,transplantation,c-Met/HGFR,HGF,Inhibitor
CBNumber:
CB54868672
Molecular Formula:
C9H8N2S
Molecular Weight:
176.24
MDL Number:
MOL File:
1070881-42-3.mol
Last updated:2023-10-23 08:51:09

Terevalefim Properties

Boiling point 369.3±11.0 °C(Predicted)
Density 1.318±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 100 mg/mL (567.41 mM; Need ultrasonic)
pka 14.05±0.10(Predicted)
FDA UNII GG91UXK2M5

Terevalefim Chemical Properties,Uses,Production

Description

Terevalefim (ANG-3777) is a hepatocyte growth factor (HGF) mimetic that in preclinical and phase 2 studies has demonstrated the ability to activate the c-Met receptor and the pathways associated with that activation, improving renal function in induced-AKI in animals and long-term graft function occurring in renal transplantation recipients with signs of DGF[1-2].

Biological Functions

ANG-3777 (Terevalefim) is an HGF mimetic that in vitro induces the same c-Met cascades and cellular effects as endogenous HGF. In animals, ANG-3777 stimulates tubular repair and regeneration, resulting in improved renal function following ischemia reperfusion injury. In humans, ANG-3777 has been shown to improve renal function up to 1 year after kidney transplantation in patients with signs of delayed graft function[1].

in vitro

In vitro, ANG-3777 reduces apoptosis and increases cell proliferation, migration, morphogenesis, and angiogenesis in injured kidneys. In animal models, ANG-3777 mitigates the effects of renal damage secondary to ischemia reperfusion injury and nephrotoxic chemicals[1].

in vivo

In vivo, Terevalefim results in dimerization and phosphorylation, and thus activation of the c-Met receptor, followed by activation of c-Met signaling cascades. The presence of c-Met is needed for ANG-3777 activity, and ANG-3777 selectively phosphorylates c-Met. Furthermore, c-Met phosphorylation induced by ANG-3777 occurs in a dose- and time-dependent manner with selective phosphorylation of c-Met and its downstream effector of ERK. No phosphorylation of IFGR, Tie2, EGFR, or FGFR occurs[2].

References

[1] Ayad S, et al. Hepatocyte Growth Factor Mimetic ANG-3777 for Cardiac Surgery–Associated Acute Kidney Injury. Kidney International Reports, 2020; 5: 2325–2332.
[2] Vincenti F, et al. Phase 3 trial design of the hepatocyte growth factor mimetic ANG-3777 in renal transplant recipients with delayed graft function. Kidney International Reports, 2021; 6: 296-303.

Terevalefim Preparation Products And Raw materials

Raw materials

Preparation Products

Terevalefim Suppliers

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Gubang New Materail Technology Co. LTD
21-51317962 +8618721305404 16728589@qq.com CHINA 272 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
Shanghai Gugang New Materials Technology Co. Ltd. 021-51317962 296935822@qq.com China 965 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24131 58
Shanghai?Medlife?Pharm-Tech?Co.,?Ltd 021-59167510 18117107507 vip@med-life.cn China 5019 58
RD International Technology Co., Limited 18988968278 sales@ubiochem.com China 9146 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 15850508050 cindy.huang@synzest.com China 12007 58
Terevalefim 3-[(E)-2-(thiophen-2-yl)ethenyl]-2H-pyrazole 1H-Pyrazole, 3-[(1E)-2-(2-thienyl)ethenyl]- (E)-3-(2-(thiophen-2-yl)vinyl)-1H-pyrazole Terevalefim(ANG-3777) ANG-3777,Terevalefim,injury,acute,inhibit,ANG 3777,AKI,kidney,ANG3777,transplantation,c-Met/HGFR,HGF,Inhibitor 1070881-42-3