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T1088Repaglinide；瑞格列奈AG-EE 388 ZW|||AG-EE 623ZW；AG-EE 388 ZW|||AG-EE 623ZW|||瑞格列奈
Repaglinide (AG-EE 623ZW) is a benzoic acid derivative that stimulates insulin secretion from the pancreas and is used in the therapy of type 2 diabetes. Repaglinide has been linked to rare instances of clinically apparent acute liver injury.
价 格：￥电议型 号：T1088产 地：中国大陆
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T1087LValaciclovir；化合物 T1087LValaciclovir
Valacyclovir (Valaciclovir) is an orally active antiviral drug for herpes simplex, herpes zoster, and herpes B. Valacyclovir inhibits HSV-1 W with an IC50 of 2.9 μg/ml. Valacyclovir is a prodrug of Aciclovir [1] [2] [3] [4] [5].
价 格：￥电议型 号：T1087L产 地：中国大陆
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T10878CPFX2090；化合物 T10878CPFX2090
CPFX2090, a cephalosporin antibacterial compound.
价 格：￥电议型 号：T10878产 地：中国大陆
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T10877CPDA；化合物CPDACPDA
CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).
价 格：￥电议型 号：T10877产 地：中国大陆
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T10876CPA inhibitor；化合物CPA inhibitorCarboxypeptidase inhibitor；Carboxypeptidase inhibitor
CPA inhibitor (Carboxypeptidase inhibitor) is a potent carboxypeptidase A (CPA) inhibitor with a Ki of 0.32 μM.
价 格：￥电议型 号：T10876产 地：中国大陆
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T10875CP5V；化合物 T10875CP5V
CP5V, a PROTAC, induces mitotic inhibition, and suppresses cancer cell proliferation. It specifically degrades Cdc20 by linking Cdc20 to the VHL/VBC complex for ubiquitination followed by proteasomal degradation.
价 格：￥电议型 号：T10875产 地：中国大陆
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T10874CP-060；化合物CP-060CP-060
CP-?060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
价 格：￥电议型 号：T10874产 地：中国大陆
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T10873CP-96486；化合物 T10873CP-96486
CP-96486 is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor (Kis: 20 and 24 nM).
价 格：￥电议型 号：T10873产 地：中国大陆
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T10872LCP 96021；化合物CP 96021CP 96021
CP 96021 is a group of 5-HT1 receptors and 5-HT2 receptors antagonists that have anti-inflammatory properties and are non-non-self anti-ulcer compounds for the treatment of gastrointestinal tract and respiratory asthma.
价 格：￥电议型 号：T10872L产 地：中国大陆
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T10872CP-96021 hydrochloride；化合物 T10872CP-96021 hydrochloride
CP-96021 hydrochloride is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor receptor (Kis: 34 nM and 37 nM).
价 格：￥电议型 号：T10872产 地：中国大陆
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T10871CP-809101 hydrochloride；2-[(3-氯苯基)甲氧基]-6-(1-哌嗪基)吡嗪盐酸盐CP-809101 hydrochloride
CP-809101 hydrochloride is a potent and selective 5-HT2C receptor agonist (pEC50: 9.96/7.19/6.81 for human 5-HT2C/5-HT2B/5-HT2A receptors).
价 格：￥电议型 号：T10871产 地：中国大陆
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T10870LCP-547632；化合物CP-547632CP-547632
CP-547632 is an orally available and potent, ATP-competitive dual inhibitor of VEGFR-2 and FGF kinase F with IC50s of 11 nM and 9 nM, respectively. CP-547632 is selective, with higher selectivity for VEGFR2 and bFGF than for EGFR, PDGFRβ and related tyrosine kinases (TKs). PDGFRβ and related tyrosine kinases (TKs) CP-547632 has antitumour activity.
价 格：￥电议型 号：T10870L产 地：中国大陆
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T10870CP-547632 hydrochloride；化合物 T10870CP-547632 hydrochloride
CP-547632 hydrochloride is a well-tolerated and orally-bioavailable inhibitor of the VEGFR-2 and basic FGF kinases (IC50s: 11 nM and 9 nM) with antitumor efficacy.
价 格：￥电议型 号：T10870产 地：中国大陆
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T1087Valacyclovir hydrochloride；盐酸伐昔洛韦Valaciclovir hydrochloride|||Valaciclovir HCl；Valaciclovir hydrochl
Valacyclovir hydrochloride (Valaciclovir hydrochloride) is an acyclovir prodrug that inhibits viral DNA replication after metabolization.
价 格：￥电议型 号：T1087产 地：中国大陆
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T10869LCP-409092；化合物 T10869LCP-409092
CP-409092 is a partial GABAA receptor agonist. It has anti-anxiety activity.
价 格：￥电议型 号：T10869L产 地：中国大陆
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T10869CP-409092 hydrochloride；化合物 T10869CP-409092 hydrochloride
CP-409092 hydrochloride is a partial agonist of the GABAA receptor with anti-anxiety activity.
价 格：￥电议型 号：T10869产 地：中国大陆
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T10868CP-28888；化合物 T10868CP 28888-27；CP 28888-27
CP-28888, an interferon inducer, exhibits heightened potency in mice compared to humans and lacks antirhinovirus effects.
价 格：￥电议型 号：T10868产 地：中国大陆
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T10867Coumetarol库美香豆素Ph 137|||Dicumoxane|||库美香豆素
Coumetarol is an antagonist of vitamin K.
价 格：￥电议型 号：T10867产 地：中国大陆
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T10866Cot inhibitor-2；Cot抑制剂2Cot inhibitor-2
Cot inhibitor-2 is a cot (Tpl2/MAP3K8) inhibitor (IC50: 1.6 nM) with potency, selectivity and oral activity. cot inhibitor-2 inhibits LPS-stimulated TNF-α production in human whole blood with an IC50 of 0.3 μM.
价 格：￥电议型 号：T10866产 地：中国大陆
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T10865LCot inhibitor-1 hydrochloride；化合物Cot inhibitor-1盐酸盐Cot inhibitor-1 hydrochloride(915365-57-0 Free ba
Cot inhibitor-1 hydrochloride is an inhibitor of tumor progression loci-2 kinase (IC50 = 28 nM) and inhibits the production of TNF-α in human whole blood (IC50 = 5.7 nM).
价 格：￥电议型 号：T10865L产 地：中国大陆
