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T11769KRAS G12C inhibitor 15；化合物 T11769KRAS G12C inhibitor 15
KRAS G12C inhibitor 15 is a potent KRAS G12C inhibitor .
价 格：￥电议型 号：T11769产 地：中国大陆
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T11768KRAS G12C inhibitor 14化合物 T11768KRAS G12C inhibitor 14|||KRAS G-12C inhibitor 14
KRAS G12C inhibitor 14 is a potent KRAS G12C inhibitor with an IC 50 of 18 nM [1].
价 格：￥电议型 号：T11768产 地：中国大陆
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T11767KRAS G12C inhibitor 13；化合物 T11767KRAS G12C inhibitor 13
KRAS G12C inhibitor 13 is a KRAS G12C inhibitor .
价 格：￥电议型 号：T11767产 地：中国大陆
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T11766LEltanexor；化合物EltanexorONO-7706|||KPT-8602|||ATG-016；ONO-7706|||KPT-8602|||ATG-016
Eltanexor (ONO-7706) is an orally active exportin-1 (XPO1) inhibitor. It has effective anti-leukemic activity. Eltanexor inhibits XPO1-dependent nuclear export (EC50=60.9 nM) by directly targeting XPO1. Eltanexor causes caspase-dependent apoptosis in a panel of leukemic cell lines.
价 格：￥电议型 号：T11766L产 地：中国大陆
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T11766Eltanexor Z-isomer化合物 T11766KPT-8602 (Z-isomer)
Eltanexor Z-isomer exhibits different inhibitory effects on Z138, MM15, 3T3 cell lines, with IC50s of 100 nM-50 μM, < 100 nM, > 30 μM, respectively.Eltanexor Z-isomer is the less active isomer of KPT-8602. KPT-8602 is a potent CRM1 inhibitor.
价 格：￥电议型 号：T11766产 地：中国大陆
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T11765KPLH1130；化合物KPLH1130KPLH1130
KPLH1130, a specific pyruvate dehydrogenase kinase (PDK) inhibitor, enhances glucose tolerance in mice fed a high-fat diet (HFD). It effectively hinders macrophage polarization and mitigates proinflammatory reactions.
价 格：￥电议型 号：T11765产 地：中国大陆
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T11764KP496；化合物 T11764KP496
KP496 is a selective, dual antagonist for Thromboxane A2 receptor and Leukotriene D4 receptor.
价 格：￥电议型 号：T11764产 地：中国大陆
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T11763Ko-3290；化合物 T11763Ko-3290
Ko-3290 is a cardioselective antagonist of β-adrenoceptors known for its antilipolytic effects in animals.
价 格：￥电议型 号：T11763产 地：中国大陆
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T11762LKira8；化合物Kira8AMG-18；AMG-18
Kira8 (AMG-18) is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity (IC50: 5.9 nM).
价 格：￥电议型 号：T11762L产 地：中国大陆
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T11762Kira8 Hydrochloride；化合物 T11762AMG-18 Hydrochloride；AMG-18 Hydrochloride
Kira8 Hydrochloride is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC50 of 5.9 nM.
价 格：￥电议型 号：T11762产 地：中国大陆
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T11761Tarlox-TKI；化合物 Tarlox-TKIKinase inhibitor-1；Kinase inhibitor-1
Tarlox-TKI (Kinase inhibitor-1) is a pan-ErbB inhibitor, the active ingredient of Tarloxotinib, with antitumor activity.Tarlox-TKI inhibits NRG1 and suppresses HER2 mutants.
价 格：￥电议型 号：T11761产 地：中国大陆
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T11760KIN101；3-(4-溴苯基)-4-氧代-7-[(甲磺酰基)氧基]-4H-色烯3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene；
KIN101 (3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene), an isoflavone agonist of IRF-3 dependent signaling, induces IRF-3 nuclear translocation. KIN101 has antiviral activity against RNA viruses, HCV, and RSV.
价 格：￥电议型 号：T11760产 地：中国大陆
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T1176Racecadotril；消旋卡多曲Acetorphan；Acetorphan|||消旋卡多曲
Racecadotril (Acetorphan) has been investigated for the basic science and treatment of Diarrhea, Acute Diarrhea, and Acute Gastroenteritis.
价 格：￥电议型 号：T1176产 地：中国大陆
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T11676Iriflophenone 3-C-glucoside；化合物Iriflophenone 3-C-glucosideIriflophenone 3-C-β-D-glucopyranoside；Irif
Iriflophenone 3-C-glucoside (Iriflophenone 3-C-β-D-glucopyranoside),has antioxidant activity,isolated from Cyclopia genistoides.
价 格：￥电议型 号：T11676产 地：中国大陆
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T11661INT-767；化合物 INT-767INT-767
INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.
价 格：￥电议型 号：T11661产 地：中国大陆
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T11601Ibrutinib-d5；化合物 T11601PCI-32765 D5|||Ibrutinib D5；PCI-32765 D5|||Ibrutinib D5
Ibrutinib D5 is a deuterium-labeled Ibrutinib. Ibrutinib is an irreversible Btk inhibitor.
价 格：￥电议型 号：T11601产 地：中国大陆
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T11576HSL-IN-1；化合物 T11576HSL-IN-1
HSL-IN-1 is an orally active hormone-sensitive lipase (HSL) inhibitor (IC50: 2 nM) with a significantly reduced reactive metabolite liability.
价 格：￥电议型 号：T11576产 地：中国大陆
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T11521GW 766994；化合物 T11521GW 994；GW 994
GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist. It has the potential for asthma and eosinophilic bronchitis treatment.
价 格：￥电议型 号：T11521产 地：中国大陆
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T11519GW768505A free base；化合物 T11519GW768505A free base
GW768505A free base is a potent dual inhibitor of VEGFR2 (KDR) and Tie-2 (pIC50: 7.81 for VEGFR2) with anti-angiogenic activity.
价 格：￥电议型 号：T11519产 地：中国大陆
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T11494GSK3532795；化合物 T11494BMS-955176；BMS-955176
GSK3532795 is a potent, orally active, second-generation HIV-1 maturation inhibitor (EC50s: 10.2, 1.9, 2.7, and 13 nM for HIV-1 WT(human serum), HIV-1 WT, HIV-1 V370A, and HIV-1 ΔV370).
价 格：￥电议型 号：T11494产 地：中国大陆
