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T10813Cilobradine hydrochloride；西洛雷定盐酸盐DK-AH 269；DK-AH 269
Cilobradine hydrochloride (DK-AH 269) is an HCN Channel blocker and an open channel blocker of neuronal Ih and related cardiac If channels.
价 格：￥电议型 号：T10813产 地：中国大陆
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T10713CCR4 antagonist 2；化合物 T10713CCR4 antagonist 2
CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg trafficking into the Tumor Microenvironment without suppressing the number of Treg in healthy tissues. CCR4 antagonist 2 (Compound 31) exhibits IC50 values of Ca2+flux and (chemotaxis) CTX are 40 nM and 70 nM, respectively.
价 格：￥电议型 号：T10713产 地：中国大陆
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T10699L2CBB1007 trihydrochloride (1379573-92-8 free base)；化合物 T10699L2CBB1007 trihydrochloride；CBB1007 trihy
CBB1007 trihydrochloride is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699L2产 地：中国大陆
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T10699CBB1007 hydrochloride (1379573-92-8 free base)；化合物 T10699CBB1007 hydrochloride；CBB1007 hydrochloride
CBB1007 Hcl is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699产 地：中国大陆
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T10698LCBB1003 hydrochloride (1379573-88-2 free base)；化合物 T10698LCBB1003 hydrochloride；CBB1003 hydrochlorid
CBB1003 hydrochloride is a new inhibitor of histone demethylase LSD1 (IC50: 10.54 μM).
价 格：￥电议型 号：T10698L产 地：中国大陆
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T10660L2CAL-130 Racemate；化合物 T10660L2CAL-130 Racemate
CAL-130 Racemate is the racemate of CAL-130. CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660L2产 地：中国大陆
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T10660LCAL-130 Hydrochloride；化合物 T10660LCAL-130 Hydrochloride
CAL-130 Hydrochloride is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660L产 地：中国大陆
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T10660CAL-130；化合物 T10660CAL-130
CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660产 地：中国大陆
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T10655c-Met inhibitor 1化合物c-Met inhibitor 13-[(2-甲基-2H-吲唑-5-基)硫基]-6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪
c-Met inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including glioblastoma, gastric, and pancreatic cancer.
价 格：￥电议型 号：T10655产 地：中国大陆
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T10631Bucindolol布新洛尔BMY 13105|||MJ 131051|||MJ 13105
Bucindolol (BMY 13105) is a novel and potent β1-adrenergic receptor blocker that mediates vasodilation and can be used to study chronic heart failure.
价 格：￥电议型 号：T10631产 地：中国大陆
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T10628BTK inhibitor 13；化合物 T10628BTK inhibitor 13
BTK inhibitor 13 (compound 8) is an effective and selective BTK inhibitor(IC50: 1.2 nM).
价 格：￥电议型 号：T10628产 地：中国大陆
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T10624BT-13；化合物BT-13BT-13
BT-13 is a selective agonist of glial cell line-derived neurotrophic factor (GDNF) receptor RET independently of GFLs. BT-13 promotes neurite growth from sensory neurons in vitro.
价 格：￥电议型 号：T10624产 地：中国大陆
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T10617Brofaromine；化合物 T10617CGP 11305A；CGP 11305A
Brofaromine (CGP 11305A) is an MAO inhibitor (IC50: 0.2 μM for MAO-A).
价 格：￥电议型 号：T10617产 地：中国大陆
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T10613BRL 37344 sodium；化合物 T10613BRL 37344A；BRL 37344A
BRL 37344 sodium is a specific agonist of the β3-adrenergic receptor. The treatment of BRL 37344 sodium significantly lowers the bodyweight of obese mice.
价 格：￥电议型 号：T10613产 地：中国大陆
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T10586LBPH-1358；化合物BPH-1358NSC50460；NSC50460
BPH-1358 (NSC-50460) (NSC-50460) is a potent human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS) inhibitor. With IC50s of 1.8 μM and 110 nM, respectively. And it is active against S. aureus in vitro (MIC ~250 ng/mL)[1][2].
价 格：￥电议型 号：T10586L产 地：中国大陆
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T10586BPH-1358 free base；化合物 T10586NSC50460 free base；NSC50460 free base
BPH-1358 (NSC50460) free base is a potent human undecaprenyl diphosphate synthase (UPPS) and farnesyl diphosphate synthase (FPPS) inhibitor (IC50s: 110 nM and 1.8 μM) and is active against S. aureus in vitro (MIC ~250 ng/mL).
价 格：￥电议型 号：T10586产 地：中国大陆
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T10562(4-Acetamidocyclohexyl) nitrate；化合物 T10562BM121307；BM121307
(4-Acetamidocyclohexyl) nitrate (BM121307) is an activator of guanylate cyclase.
价 格：￥电议型 号：T10562产 地：中国大陆
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T10561BM-131246；化合物BM-131246BM-131246
BM-131246 is an orally available and antidiabetic active thiazolidinedione derivative for the study of diabetes.
价 格：￥电议型 号：T10561产 地：中国大陆
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T10556BKI-1369；化合物 T10556BKI-1369
BKI-1369 is a bumped kinase inhibitor. BKI-1369 increases hERG-inhibitory activity (IC50:1.52 μM).
价 格：￥电议型 号：T10556产 地：中国大陆
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T10513Benzothiohydrazide化合物 BenzothiohydrazideBenzothiohydrazide
Benzothiohydrazide is an analog of isoniazid with anti-tuberculosis activity and can be used to isolate fungi and bacteria.
价 格：￥电议型 号：T10513产 地：中国大陆
