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T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
价 格：￥电议型 号：T11675产 地：中国大陆
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T11647INCB 3284 dimesylate；化合物 T11647INCB 3284 dimesylate
INCB 3284 dimesylate is a selective and orally bioavailable human CCR2 antagonist, inhibiting monocyte chemoattractant protein-1 binding to hCCR2 (IC50: 3.7 nM). It can be used in the research of acute liver failure.
价 格：￥电议型 号：T11647产 地：中国大陆
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T11597LIACS-9571 Hydrochloride (1800477-30-8 free base)；化合物 T11597LIACS-9571 Hydrochloride|||ASIS-P040 Hydr
IACS-9571 Hydrochloride is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
价 格：￥电议型 号：T11597L产 地：中国大陆
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T11547hDHODH-IN-2；化合物 T11547hDHODH-IN-2
hDHODH-IN-2 is an analogue of the active metabolite of Leflunomide. hDHODH-IN-2 is a human dihydroorotate dehydrogenase (hDHODH) inhibitor with anti-inflammatory activity.
价 格：￥电议型 号：T11547产 地：中国大陆
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T11493GSK3004774；化合物 T11493GSK3004774
GSK3004774 is a nonabsorbable agonist of CaSR (pEC50: 7.3, 6.6, and 6.5 for human, mouse, and rat CaSR). GSK3004774 shows an EC50 of 50 nM for human CaSR.
价 格：￥电议型 号：T11493产 地：中国大陆
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T11479GSK1521498；化合物 T11479GSK1521498
GSK1521498 is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11479产 地：中国大陆
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T11478LGSK1521498 free base；化合物 T11478LGSK1521498 free base
GSK1521498 free base is a potent and selective antagonist of the μ-opioid receptor. GSK1521498 free base also has the potential for disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478L产 地：中国大陆
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T11478GSK1521498 free base (hydrochloride)；化合物 T11478GSK1521498 free base (hydrochloride)
GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478产 地：中国大陆
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T11477GSK1059865；化合物 T11477GSK1059865
GSK1059865 is a potent antagonist of the orexin 1 receptor.
价 格：￥电议型 号：T11477产 地：中国大陆
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T11476GSK-J2；化合物 T11476GSK-J2
GSK-J2, an isomer of GSK-J1, haven´t any specific activity. GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A.
价 格：￥电议型 号：T11476产 地：中国大陆
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T11475GSK-J1 lithium salt化合物 T11475GSKJ1 lithium salt|||GSK J1 lithium salt|||GSK-J-1 lithium salt
GSK-J1 lithium salt is an effective inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with an IC 50 of 60 nM for KDM6B.
价 格：￥电议型 号：T11475产 地：中国大陆
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T11472LMolibresib besylate化合物 T11472LI-BET 762 besylate|||GSK 525762C
Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM).
价 格：￥电议型 号：T11472L产 地：中国大陆
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T11472GSK 525768A；化合物 T11472GSK 525768A
GSK 525768A, the inactive enantiomer of GSK525762A, exhibits no activity towards BET.
价 格：￥电议型 号：T11472产 地：中国大陆
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T11471GSK-3β inhibitor 2；GSK-3β 抑制剂 25-Thiazolecarboxamide,2-[2-[(cyclopropylcarbonyl)amino]-4-pyridinyl]-
GSK-3β inhibitor 2 (5-Thiazolecarboxamide,2-[2-[(cyclopropylcarbonyl)amino]-4-pyridinyl]-4-methoxy-) is a BBB-crossing and selective inhibitor of GSK-3β (IC50 = 1.1 nM). GSK-3β inhibitor 2 can be used in studies about Alzheimer´s disease.
价 格：￥电议型 号：T11471产 地：中国大陆
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T11470GSK 366；化合物 T11470GSK 366
GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor (IC50s: 0.7 nM and 2.3 nM for P. fluorescens-KMO and human KMO).
价 格：￥电议型 号：T11470产 地：中国大陆
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T1147Chlorhexidine dihydrochloride；盐酸氯己定Chlorhexidine hydrochloride|||Chlorhexidine 2HCl|||NSC-185；盐酸氯己定|
Chlorhexidine dihydrochloride (NSC-185) is a disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque.
价 格：￥电议型 号：T1147产 地：中国大陆
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T11447GNF4877；化合物GNF4877GNF4877
GNF4877 is a potent DYRK1A and GSK3β inhibitor (IC50s: 6 nM and 16 nM). It leads to blockade of nuclear factor of activated T-cells (NFATc) nuclear export and increased β-cell proliferation cells.
价 格：￥电议型 号：T11447产 地：中国大陆
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T11402LGKI-1 HCl；GKI-1盐酸盐GKI-1 HCl（ 2444764-03-6 Free base）；GKI-1 HCl（ 2444764-03-6 Free base）
GKI-1 HCl is a Greatwall (GWL) kinase inhibitor that inhibits hGWLFL and hGWL-KinDom.The inhibitory effect of GKI-1 HCl on ROCK1 is more significant.
价 格：￥电议型 号：T11402L产 地：中国大陆
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T11347G6PD activator AG1；化合物 T11347G6PD activator AG1
G6PD activator AG1 is a glucose-6-phosphate dehydrogenase (G6PD) activator with an EC50 of 3 μΜ.
价 格：￥电议型 号：T11347产 地：中国大陆
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T11321FR194738 free base；化合物FR194738 free baseFR194738 free base
FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.?
价 格：￥电议型 号：T11321产 地：中国大陆
