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产品数：86101
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T23350SGS518 oxalate；化合物 T23350SGS 518 oxalate；SGS 518 oxalate
SGS518 oxalate is a 5-HT6 antagonist.
价 格：￥电议型 号：T23350产 地：中国大陆
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T2293SGX-523；化合物SGX-523SGX-523
SGX-523 is a selective Met inhibitor (IC50: 4 nM), no inhibitory to Abl, BRAFV599E, p38α, and c-Raf.
价 格：￥电议型 号：T2293产 地：中国大陆
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T21077Tolperisone free base；化合物 T21077Mydeton|||Atmosgen free base|||Mideton|||Menopatol|||Besnoline free
Tolperisone free base, a centrally acting muscle relaxant, has been used for the symptomatic treatment of spasticity and muscle spasm.
价 格：￥电议型 号：T21077产 地：中国大陆
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T19560SGD-1882；化合物 T19560PBD dimer；PBD dimer
SGD-1882 is a agent of cytotoxic, DNA minor-groove crosslinking pyrrolobenzodiazepine (PBD) dimer, and acting as the payload for ADCs.
价 格：￥电议型 号：T19560产 地：中国大陆
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T1904SGI-1027；化合物SGI-1027DNA Methyltransferase Inhibitor II|||SGI1027；DNA Methyltransferase Inhibitor II|
SGI-1027 (DNA Methyltransferase Inhibitor II) is an effective and selective inhibitor of DNA methyltransferase (DNMT). The IC50 of SGI-1027(SGI1027) against DNMT1, DNMT3A, and DNMT3B are 6, 8, 7.5 μM, respectively.
价 格：￥电议型 号：T1904产 地：中国大陆
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T17175Troxacitabine；化合物 T17175BCH-4556|||SGX-145|||SGX145|||SPD-758|||BCH4556|||beta-L-OddC；BCH-4556|||SGX
Troxacitabine, a DNA polymerase inhibitor, is potentially used for the treatment of acute myeloid leukemia (AML). In comparison with gemcitabine, troxacitabine was equally active against MiaPaCa and was more efficacious against Panc-01.
价 格：￥电议型 号：T17175产 地：中国大陆
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T16876Guadecitabine；化合物 T16876SGI-110；SGI-110
Guadecitabine is a second-generation DNA methyltransferases inhibitor. It is used for research on acute myeloid leukemia and myelodysplastic syndromes.
价 格：￥电议型 号：T16876产 地：中国大陆
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T16025SGD-1910；化合物 T16025MC-Val-Ala-PBD；MC-Val-Ala-PBD
MC-Val-Ala-PBD is a drug-linker conjugate for ADC by using the antitumor antibiotic, pyrrolobenzodiazepine (PBD, a cytotoxic DNA crosslinking), linked via the cleavable linker MC-Val-Ala[1].
价 格：￥电议型 号：T16025产 地：中国大陆
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T15171DSG Crosslinker；双琥珀酰亚胺戊二酸酯DSG Crosslinker
DSG Crosslinker is a cleavable ADC linker used in antibody-drug conjugates (ADCs) synthesis.
价 格：￥电议型 号：T15171产 地：中国大陆
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T13936Triptotriterpenic acid A；化合物 T13936Maytenfolic acid|||Abrusgenic acid；Maytenfolic acid|||Abrusgenic
Triptotriterpenic acid A is a natural product isolate from Tripterygium wilfordii.
价 格：￥电议型 号：T13936产 地：中国大陆
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T13847PROTAC SGK3 degrader-1；PROTAC SGK3 降解剂1SGK3-PROTAC1；SGK3-PROTAC1
PROTAC SGK3 degrader-1 (SGK3-PROTAC1) is a PROTAC coupler that targets SGK3 and binds ligand to VH032 VHL, which induces degradation of endogenous SGK3.PROTAC SGK3 degrader-1 inhibits GDC0941-induced proliferation of cancer cells.CAS ??5017-88-83-4
价 格：￥电议型 号：T13847产 地：中国大陆
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T13667LDusquetide；化合物 T13667LSGX942；SGX942
Dusquetide is a first-in-class innate defense regulator. Dusquetide displays activity in both reducing inflammation and increasing the clearance of bacterial infection.
价 格：￥电议型 号：T13667L产 地：中国大陆
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T13667Dusquetide TFA (931395-42-5 free base)；化合物 T13667SGX942 TFA|||Dusquetide TFA；SGX942 TFA|||Dusquetide
Dusquetide TFA is a kind of innate defense regulator (IDR).Dusquetide TFA has been shown to be active in reducing inflammation and increasing clearance of bacterial infections.Dusquetide TFA regulates innate immune responses to PAMPs and DAMPs in combination with P62.
价 格：￥电议型 号：T13667产 地：中国大陆
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T13179Tofogliflozin；化合物 T13179CSG452；CSG452
Tofogliflozin is a highly specific inhibitor of sodium/glucose cotransporter 2 (SGLT2) (Kis: 2.9, 14.9, and 6.4 nM for human, rat, and mouse SGLT2. IC50s: 2.9/14.9/6.4 nM (human/rat/mouse SGLT2)).
价 格：￥电议型 号：T13179产 地：中国大陆
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T12894SGN-2FF；化合物SGN-2FFSGN-2FF
SGN-2FF is an oral fucosyltransferase inhibitor with antitumor activity.
价 格：￥电议型 号：T12894产 地：中国大陆
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T12893SGLT inhibitor-1；化合物 T12893SGLT inhibitor-1
SGLT inhibitor-1 is a potentsodium glucose co-transporter proteins (SGLTs) dual inhibitor(hSGLT1 and hSGLT2 with IC50s of 43 nM and 9 nM, respectively).
价 格：￥电议型 号：T12893产 地：中国大陆
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T12892SGL5213；化合物 T12892SGL5213
SGL5213 is an oral active and low-absorbable inhibitor of sodium-dependent glucose cotransporter 1 (SGLT1)(hSGLT1 and hSGLT2 with IC50 values of 29 nM and 20 nM , respectively),and has potential to treat type 2 diabetes.
价 格：￥电议型 号：T12892产 地：中国大陆
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T12891SGK1-IN-2；化合物 T12891SGK1-IN-2
SGK1-IN-2 (14h) is a selective inhibitor of SGK1 (serum and glucocorticoid regulated kinase 1)(with an IC50 of 5 nM at 10 μM ATP concentration).
价 格：￥电议型 号：T12891产 地：中国大陆
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T12890SGK1-IN-1；化合物 T12890SGK1-IN-1
SGK1-IN-1 is a highly active and selective SGK-1 inhibitor(IC50 of 1 nM).
价 格：￥电议型 号：T12890产 地：中国大陆
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T12887SGC3027；化合物 T12887SGC3027
SGC3027 is an inhibitor of histone methyltransferase,also is a first potent, selective and cell active chemical probe for PRMT7.
价 格：￥电议型 号：T12887产 地：中国大陆
