MTX115325

MTX115325 Suppliers list
Company Name: Chunchuang (Wuhan) Technology Co., Ltd  
Tel: 15727060112
Email: yutianchun2007@126.com
Company Name: NewCan Biotech Limited  
Tel: +86-0571-86912261 +86-15658003402
Email: sales@newcanbio.com
Company Name: Suzhou Haiben Pharmaceutical Co., Ltd  
Tel: 19353112242
Email: 1816280386@qq.com
Company Name: SuZhou GoodChemTech Co., Ltd  
Tel: 18136139868; 18136139868
Email: jinlun@goodchemtech.cn
Company Name: Nantong Hanfang Biotechnology Co. , Ltd.  
Tel: hanfangpharma@126.com 18017580634
Email: hanfangpharma@126.com
MTX115325 Basic information
Product Name:MTX115325
Synonyms:MTX115325;Pyrrolo[3,4-b]pyrrole-5(1H)-carbonitrile, 1-[[5-(2-cyano-4-pyridinyl)-2-oxazolyl]carbonyl]hexahydro-4-methyl-, (3aR,4R,6aR)-
CAS:2750895-97-5
MF:C18H16N6O2
MW:348.36
EINECS:
Product Categories:
Mol File:2750895-97-5.mol
MTX115325 Structure
MTX115325 Chemical Properties
Boiling point 626.880±65.00 °C(Press: 760.00 Torr)(predicted)
density 1.439±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka-2.380±0.10(predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
MTX115325 Usage And Synthesis
UsesMTX115325 (Example 1) is an orally active, brain-penetrating USP30 inhibitor (IC50=12 nM) with neuroprotective activity. MTX115325 increases ubiquitination (EC50=32 nM) of the mitochondrial outer membrane protein TOM20 (a USP30 substrate), increasing mitophagy. MTX115325 prevents dopaminergic neuron loss and preserves striatal dopamine[1].
in vivo

MTX115325 (i.g.; 15 mg/kg and 50 mg/kg; twice daily for 10 weeks) reduces phosphorylated S129-αSyn levels and decreases the total area of GFAP staining in AAV-A53T-SNCA Mouse Model, indicating lower astrocyte activation[1].
MTX115325 (i.g.; 10 mg/kg; single dose) demonstrates excellent oral bioavailability (98%) and good CNS penetration with a brain partition coefficient (Kpu,u) of approximately 0.4[1].
MTX115325 (i.g.; single dose) has a Cmax of 7546.9 ng/mL at 15 mg/kg and a Cmax of 16374.3 ng/mL at 50 mg/kg. At a 50 mg/kg dosage, the drug concentration consistently remained above the EC50 for TOM20 ubiquitination[1].

Animal Model:AAV-A53T-SNCA Mouse Model [1]
Dosage:15 mg/kg and 50 mg/kg
Administration:i.g.; twice daily for 10 weeks
Result:Reduced the loss of dopaminergic neurons in the substantia nigra (SN) and preserved dopamine levels in the striatum.
Increased the percentage of tyrosine hydroxylase (TH)+ neurons.
References[1] Fang TZ et al. Knockout or inhibition of USP30 protects dopaminergic neurons in a Parkinson's disease mouse model. Nat Commun. 2023 Nov 13;14(1):7295. DOI:10.1038/s41467-023-42876-1
MTX115325 Preparation Products And Raw materials
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