Thalidomide

Inkcazelo emfutshane:

Igama le-API Isalathiso Inkcazo I-USDMF EU DMF CEP
Thalidomide Iyeza le-Oncology USP/EP      


Iinkcukacha zeMveliso

Iithegi zeMveliso

IINKCUKACHA ZEMVELISO

Imvelaphi

I-Thalidomide yaziswa njengechiza lokuthomalalisa, i-immunomodulatory agent kwaye iphandwa ukunyanga iimpawu zomhlaza ezininzi.,eyi-CRBN-DDB1-Cul4A complex.

Inkcazo

I-Thalidomide ikhuthazwa ekuqaleni njenge-sedative, inhibits cereblon (CRBN), inxalenye ye-cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1, kunye ne-Kd250 nM, kwaye ine-immunomodulatory, anti-inflammatory kunye ne-anti-angiogenic cancer cancer properties.

I-In vitro

I-Thalidomide ikhuthazwa ekuqaleni njenge-sedative, ine-immunomodulatory, i-anti-inflammatory kunye ne-anti-angiogenic properties, kwaye ijolise kwi-cereblon (CRBN), inxalenye ye-cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1, kunye ne-Kd250 nM[1]. IThalidomide (50μi-g / mL) ibangela umsebenzi wokulwa ne-tumor we-icotinib ngokuchasene nokunyuka kwe-PC9 kunye neeseli ze-A549, kwaye esi siphumo sihambelana ne-apoptosis kunye nokufuduka kweeseli. Ukongezelela, i-Thalidomide kunye ne-icotinib inqanda i-EGFR kunye ne-VEGF-R2 iindlela kwiiseli ze-PC9 [3].

I-Thalidomide (i-100 mg / kg, i-po) inqanda ukufakwa kwe-collagen, phantsi-ilawula inqanaba lokubonisa i-mRNAα-SMA kunye ne-collagen I, kwaye iyanciphisa kakhulu i-cytokines e-pro-inflammatory kwiigundane ze-RILF. I-Thalidomide inciphisa i-RILF ngokucinezela i-ROS kunye nolawulo oluphantsi lwe-TGF-β/Indlela yeSmad ixhomekeke kwisimo se-Nrf2[2]. I-Thalidomide (200 mg/kg, po) idityaniswe ne-icotinib ibonisa iziphumo ze-synergistic anti-tumor kwiimpuku ezihamba ze ezithwele iiseli ze-PC9, ukucinezela ukukhula kwethumba kunye nokukhuthaza ukufa kwethumba[3].

Ugcino

Umgubo

-20°C

Iminyaka emi-3

4°C

iminyaka eyi-2
Kwi-solvent

-80°C

Iinyanga ezi-6

-20°C

Inyanga eyi-1

Ubume beMichiza

Thalidomide

ISIQINISEKISO

2018 GMP-2
原料药GMP证书201811(captopril,thalidomide etc)
GMP-of-PMDA-in-Chanyoo-平成28年08月03日 Nantong-Chanyoo-Pharmatech-Co
I-FDA-EIR-Letter-201901

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