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T62491STAT3-IN-13；STAT3抑制剂13STAT3-IN-13
STAT3-IN-13 is a potent STAT3 inhibitor.STAT3-IN-13 has antiproliferative and anticancer activity and acts by binding to the structural domain of STAT3 SH2.STAT3-IN-13 inhibits the phosphorylation of STAT3 Y705, which induces apoptosis and inhibits tumor cell growth and metastasis.STAT3-IN-13 can be used to study breast cancer and liver cancer. The study of breast cancer and hepatocellular carcinoma.
价 格：￥电议型 号：T62491产 地：中国大陆
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T62490OBHS；化合物 OBHSOBHS
OBHS is an inhibitor of estrogen receptor alpha (ERα).
价 格：￥电议型 号：T62490产 地：中国大陆
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T6249Avagacestat；化合物AvagacestatBMS-708163；BMS-708163
Avagacestat (BMS-708163) (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.
价 格：￥电议型 号：T6249产 地：中国大陆
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T62489MAGL-IN-6；化合物 MAGL-IN-6MAGL-IN-6
MAGL-IN-6 is a potent inhibitor of MAGL (IC50: 4.71 nM). MAGL-IN-6 can be used to study neurological diseases.
价 格：￥电议型 号：T62489产 地：中国大陆
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T62488P2X7 receptor antagonist-1；化合物 P2X7 receptor antagonist-1P2X7 receptor antagonist-1
P2X7 receptor antagonist-1 is a purinergic P2X7 receptor antagonist with anti-neuroinflammatory effects.
价 格：￥电议型 号：T62488产 地：中国大陆
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T62487HER2-IN-12；化合物 HER2-IN-12HER2-IN-12
HER2-IN-12 is an HER2 inhibitor with an IC50 value of 121 nM and can be used to study cancers such as breast cancer.
价 格：￥电议型 号：T62487产 地：中国大陆
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T62486VIM-2-IN-1；化合物 VIM-2-IN-1VIM-2-IN-1
VIM-2-IN-1 (compound 1dj) is a β-lactamase inhibitor with antibacterial activity. IC50: 48 μM) and New Delhi Metal (NDM-1) (IC50: 231 μM).
价 格：￥电议型 号：T62486产 地：中国大陆
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T62485FabG1-IN-1；化合物 FabG1-IN-1FabG1-IN-1
FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).
价 格：￥电议型 号：T62485产 地：中国大陆
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T62484Aurora Kinases-IN-2；化合物 Aurora Kinases-IN-2Aurora Kinases-IN-2
Aurora Kinases-IN-2 (compound 12Aj) is a potent inhibitor of Aurora kinases, acting on Aurora A (IC50: 90 nM) and Aurora B (IC50: 152 nM). Aurora Kinases-IN-2 can be used in cancer research.
价 格：￥电议型 号：T62484产 地：中国大陆
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T62483CJJ300；化合物CJJ300CJJ300
CJJ300 is a transforming growth factor-β (TGF-β) inhibitor (IC50 : 5.3 μM).CJJ300 inhibits TGF-β signaling by disrupting the formation of the TGF-β-TβR-I-TβR-II signaling complex.CJJ300 inhibits cell migration.
价 格：￥电议型 号：T62483产 地：中国大陆
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T62482Sunobinop；化合物 SunobinopSunobinop
Sunobinop (S 117957) is an opioid receptor-like orphan receptor (ORL1) modulator.
价 格：￥电议型 号：T62482产 地：中国大陆
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T62480Antitumor agent-51；化合物 Antitumor agent-51Antitumor agent-51
Antitumor agent-51 is effective and selective in inhibiting the growth and migration of osteosarcoma cells, acting on MNNG/HOS cells (IC50: 21.9 nM). antitumor agent-51 is less toxic and extremely bioavailable.
价 格：￥电议型 号：T62480产 地：中国大陆
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T6248XL888；化合物XL888XL888
XL888 is an ATP-competitive inhibitor of Hsp90 ( IC50: 24 nM). Heat shock protein 90 (Hsp90) is a chaperone that maintains the functionality of client proteins involved in cell proliferation, cell cycling, and apoptosis. Through this action, specific client proteins are degraded, resulting in cell cycle arrest or apoptosis. XL888 is orally bioavailable and shows efficacy in tumor regression in gastric carcinoma and melanoma xenografts in mice.
价 格：￥电议型 号：T6248产 地：中国大陆
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T624793CPLro-IN-1；化合物 3CPLro-IN-13CPLro-IN-1
3CPLro-IN-1 (compound A17) is a potent, orally active inhibitor of SARS-CoV-2 3CLpro (IC50: 5.65 μM). 3-Chymotrypsin-like cysteine protease (3CLpro), a protein essential for viral replication, is an attractive drug target against COVID-19. Antitumor agent-51
价 格：￥电议型 号：T62479产 地：中国大陆
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T62478SOS1-IN-9；化合物 SOS1-IN-9SOS1-IN-9
SOS1-IN-9 is a potent inhibitor of SOS1 that acts on KRAS G12C-SOS1 (IC50: 116.5 nM).
价 格：￥电议型 号：T62478产 地：中国大陆
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T62477Tubulin polymerization-IN-18；化合物 Tubulin polymerization-IN-18Tubulin polymerization-IN-18
Tubulin aggregation-IN-18 (compound 3) is a potent tubulin aggregation inhibitor with potential for breast cancer and drug-resistant colon cancer studies.
价 格：￥电议型 号：T62477产 地：中国大陆
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T62476Trimazosin；化合物 TrimazosinTrimazosin
Trimazosin is an orally active quinazoline derivative, structurally related to prazosin. trimazosin has hypotensive activity by selectively blocking alpha1-adrenoceptors.
价 格：￥电议型 号：T62476产 地：中国大陆
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T62475Chitin synthase inhibitor 7；化合物 Chitin synthase inhibitor 7Chitin synthase inhibitor 7
Chitin synthase inhibitor 7 (compound 9c) is a potent inhibitor of chitin synthase (CHS) (IC50: 0.37 nM). synthase inhibitor 7 can be used to study fungal infections.
价 格：￥电议型 号：T62475产 地：中国大陆
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T62474JS1310；化合物 JS1310PRMT7-IN-1|||JS-1310；PRMT7-IN-1|||JS-1310
JS1310 is a selective PRMT7 inhibitor (IC50: 5 μM against human PRMT7). JS1310 has shown anti-cancer effects on different cancer cells.
价 格：￥电议型 号：T62474产 地：中国大陆
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T62473Edecesertib；化合物 EdecesertibEdecesertib
Edecesertib (GS-5718) is a selective, orally active IRAK-4 inhibitor that exhibits anti-inflammatory activity. edecessertib can be used to study rheumatoid arthritis (RA) and lupus erythematosus (LE).
价 格：￥电议型 号：T62473产 地：中国大陆
