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T6776BAY 61-3606 dihydrochloride；化合物BAY-61-3606BAY 61-3606|||BAY-61-3606 dihydrochloride；BAY 61-3606|||BA
BAY 61-3606 dihydrochloride (BAY 61-3606) is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
价 格：￥电议型 号：T6776产 地：中国大陆
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T66654(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane；化合物 (2b,3a,5
(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane is a useful organic compound for research related to life sciences. The catalog number is T66654 and the CAS number is 119302-24-8.
价 格：￥电议型 号：T66654产 地：中国大陆
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T66653(2b,3a,5a,16b,17b)-2-(4-Morpholinyl)-16-(1-pyrrolidinyl)androstane-3,17-diol；化合物 (2b,3a,5a,16b,17b)-
(2b,3a,5a,16b,17b)-2-(4-Morpholinyl)-16-(1-pyrrolidinyl)androstane-3,17-diol is a useful organic compound for research related to life sciences and the catalog number is T66653.
价 格：￥电议型 号：T66653产 地：中国大陆
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T6444811-Keto budesonide；化合物 (6aR,6bS,8aS,8bS,11aR,12aS,12bS)-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-10-propy
11-Keto budesonide is a useful organic compound for research related to life sciences and the catalog number is T64448.
价 格：￥电议型 号：T64448产 地：中国大陆
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T6428BV6；化合物BV6BV6
BV6 is an antagonist of c-IAP1 and XIAP, members of the inhibitors of apoptosis (IAP) family.
价 格：￥电议型 号：T6428产 地：中国大陆
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T6418BMS-378806；化合物BMS378806BMS378806|||BMS-806；BMS378806|||BMS-806|||1-[(2R)-4-苯甲酰基-2-甲基-1-哌嗪基]-2-(4-甲氧基
BMS-378806 (BMS-806) selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.
价 格：￥电议型 号：T6418产 地：中国大陆
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T64055SPOP-IN-6b dihydrochloride；化合物 SPOP-IN-6b dihydrochlorideSPOP-IN-6b dihydrochloride
SPOP-IN-6b dihydrochloride is a potent inhibitor of spotted POZ protein (SPOP) (IC50: 3.58 μM).
价 格：￥电议型 号：T64055产 地：中国大陆
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T63940B026；化合物 B026B026
B026 is a selective, orally active inhibitor of p300/CBP histone acetyltransferase (p300/CBP HAT) that acts on p300 (IC50: 1.8 nM) and CBP (IC50: 9.5 nM). b026 exhibits anticancer effects on androgen receptor positive (AR+) prostate cancer cells.
价 格：￥电议型 号：T63940产 地：中国大陆
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T63855B-Raf IN 6；化合物 B-Raf IN 6B-Raf IN 6
B-Raf IN 6 is a potent inhibitor (IC50: 1.7 nM) of the protein kinase B-Raf, which does not bind the secondary target PXR and is resistant to rapid metabolism.B-Raf IN 6 has shown research potential in cancer diseases.
价 格：￥电议型 号：T63855产 地：中国大陆
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T63676Bcl-2-IN-6；化合物 Bcl-2-IN-6Bcl-2-IN-6
Bcl-2-IN-6 is a potent inhibitor of Bcl-2 (b-cell lymphoma-2) that downregulates Bcl-2 expression and increases the expression of p53, Bax, and caspase-7 mRNA. bcl-2-IN-7 induces cell cycle arrest and apoptosis in breast cancer MCF-7 cells. bcl-2-IN-7 acts on MCF-7 cells ( Bcl2-IN-7 showed good antitumor effects on MCF-7 cells (IC50: 20.91 μM), LoVo cells (IC50: 22.30 μM), HepG2 cells (IC50: 42.29 μM) and A549 cells (IC50: 48.00 μM).
价 格：￥电议型 号：T63676产 地：中国大陆
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T63450BCR-ABL-IN-6；化合物 BCR-ABL-IN-6BCR-ABL-IN-6
BCR-ABL-IN-6 (9h) is an imatinib derivative and a selective inhibitor of Bcr-Abl kinase that acts on Bcr-AblWT (IC50: 4.6 nM) and Bcr-AblT3151 (IC50: 277 nM). BCR-ABL-IN-6 (9h) was able to be used in the study of chronic myeloid leukemia treatment.
价 格：￥电议型 号：T63450产 地：中国大陆
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T62472BTK-IN-6；化合物 BTK-IN-6BTK-IN-6
BTK-IN-6 is a potent inhibitor of Bruton´s tyrosine kinase (BTK). BTK-IN-6 has shown research potential in immune diseases, cardiovascular diseases, cancer, viral infections, inflammation, metabolic/endocrine dysfunction and neurological disorders (for more information.
价 格：￥电议型 号：T62472产 地：中国大陆
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T61785BChE-IN-6；化合物 BChE-IN-6BChE-IN-6
BChE-IN-6 (compound 12) is a highly effective inhibitor of BChE, showcasing a Ki value of 0.182 μM. Notably, BChE-IN-6 exhibits significant chelating abilities towards Zn 2+. Due to these characteristics, BChE-IN-6 serves as a valuable tool for researchers in the field of Alzheimer´s disease (AD) [1].
价 格：￥电议型 号：T61785产 地：中国大陆
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T617266BrCaQ；化合物 6BrCaQ6BrCaQ
6BrCaQ is a highly potent inhibitor of mitochondrial heat shock protein TRAP1, exhibiting significant antiproliferative properties. Additionally, 6BrCaQ can be utilized for the synthesis of 6BrCaQ-TPP conjugates [1].
价 格：￥电议型 号：T61726产 地：中国大陆
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T61455BSP16；化合物 BSP16BSP16
BSP16 is a highly potent and orally active STING agonist, capable of selectively stimulating the interferon genes pathway. This compound, BSP16, holds great potential for cancer research [1].
价 格：￥电议型 号：T61455产 地：中国大陆
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T61418BuChE-IN-6；化合物 BuChE-IN-6BuChE-IN-6
BuChE-IN-6 (compound 1b) is a highly effective and specific inhibitor of BuChE (butyrylcholinesterase), demonstrating an IC50 value of 0.46 μM for eqBuChE and 0.51 μM for hBuChE. Furthermore, BuChE-IN-6 has the additional capability of inhibiting the self-aggregation of Aβ 42 [1].
价 格：￥电议型 号：T61418产 地：中国大陆
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T6072LBGT226；化合物BGT226BGT226 free base|||NVP-BGT226；BGT226 free base|||NVP-BGT226
BGT226 (NVP-BGT226) is a novel dual PI3K / mTOR inhibitor, it acts on PI3K α/β/γ with IC50 of 4 nM / 63 nM / 38 nM, respectively.
价 格：￥电议型 号：T6072L产 地：中国大陆
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T6072BGT226 maleate；化合物BGT226BGT226|||NVP-BGT226 (maleate)|||NVP-BGT226；BGT226|||NVP-BGT226 (maleate)|||N
BGT226 maleate (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/38 nM) .
价 格：￥电议型 号：T6072产 地：中国大陆
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T60542BTK-IN-16；BTK抑制剂16BTK-IN-16
BTK-IN-16 is a potential inhibitor of wild-type BTK and C481S mutants.BTK-IN-16 can be used to study various autoimmune diseases and cancers caused by BTK.
价 格：￥电议型 号：T60542产 地：中国大陆
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T60300BPH-1086；化合物 BPH-1086BPH-1086
BPH-1086 (compound 10) is an inhibitor of IspH. IspH domain fused with ribosomal protein S1 (RPS1) can bind to mRNA or form part of the bacterial ribosome [1] [2].
价 格：￥电议型 号：T60300产 地：中国大陆
