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T27131DCG04；化合物 T27131DCG-04|||CD-892|||CD 892|||DCG 04|||CD892；DCG-04|||CD-892|||CD 892|||DCG 04|||CD892
DCG04 is a multivalent ligand for the mannose-6-phosphate receptor. DCG-04 is an activity-based probe for cysteine cathepsins, enabled fluorescent readout of its receptor-targeting properties. DCG04 is used for endolysosomal targeting of an activity-based probe.
价 格：￥电议型 号：T27131产 地：中国大陆
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T27130DCE_42；化合物 T27130DCE 42|||DCE42|||DCE-42；DCE 42|||DCE42|||DCE-42
DCE_42 is a novel EZH2 inhibitor, it also displays significant anti-proliferation activity against lymphoma cell lines.
价 格：￥电议型 号：T27130产 地：中国大陆
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T2713Stachyose tetrahydrate；水苏糖Stachyose|||D-Stachyose tetrahydrate；Stachyose|||D-Stachyose tetrahydrate|
Stachyose tetrahydrate (D-Stachyose tetrahydrate) is a tetrasaccharide consisting of two α-D-galactose units, one α-D-glucose unit, and one β-D-fructose unit sequentially.
价 格：￥电议型 号：T2713产 地：中国大陆
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T27129DCE_254；化合物 T27129DCE 254|||DCE-254|||DCE254；DCE 254|||DCE-254|||DCE254
DCE_254 is a novel EZH2 inhibitor, it also displays significant anti-proliferation activity against lymphoma cell lines.
价 格：￥电议型 号：T27129产 地：中国大陆
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T27128DCB-3503；化合物 T27128NSC716802|||NSC 716802|||NSC-716802|||DCB3503|||DCB 3503；NSC716802|||NSC 716802||
Tylophorine analog DCB-3503 is a potential anticancer and immunosuppressive agent. DCB-3503 suppresses the translation of cellular regulatory proteins, including cyclin D1, at the elongation step. DCB-3503 allosterically regulates the ATPase and chaperone activities of HSC70 by promoting ATP hydrolysis in the presence of specific RNA binding motifs (AUUUA) of cyclin D1 mRNA.
价 格：￥电议型 号：T27128产 地：中国大陆
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T27126DC07090 Dihydrochloride；化合物 T27126DC07090 Dihydrochloride
DC07090 Dihydrochloride is a potent inhibitor of human enterovirus 71 3C protease.
价 格：￥电议型 号：T27126产 地：中国大陆
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T27125DBPR-110；化合物 T27125MB110|||MB 110|||MB-110；MB110|||MB 110|||MB-110
DBPR-110 is a nonstructural protein 5A (NS5A) inhibitor. DBPR-110 reduced the reporter expression of the HCV1b replicon with a EC(50) and a selective index value of 3.9 ± 0.9 pM and >12,800,000, respectively. DBPR-110 reduced HCV2a replicon activity with an EC(50) and a selective index value of 228.8 ± 98.4 pM and >173,130, respectively.
价 格：￥电议型 号：T27125产 地：中国大陆
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T27124DB-959 (salt)；化合物 T27124T3D959|||T-3D-959|||T-3D959|||DB-959Na|||DB959Na；T3D959|||T-3D-959|||T-3D959
DB-959, a PPAR agonist, is used potentially for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T27124产 地：中国大陆
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T27123Dasolampanel etibutil；化合物 T27123Dasolampanel etibutil
Dasolampanel etibutil is a novel selective antagonist of ionotropic glutamate receptor 5 (iGluR5).
价 格：￥电议型 号：T27123产 地：中国大陆
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T27122Dasantafil；达生他非SCH446132|||SCH-446132|||SCH 446132；SCH446132|||SCH-446132|||SCH 446132
Dasantafil (SCH446132) is a small molecule phosphodiesterase-5A (PDE5A) inhibitor used to treat genitourinary disorders and study erectile dysfunction.
价 格：￥电议型 号：T27122产 地：中国大陆
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T27121Darexaban glucuronide；化合物 T27121YM 222714|||YM222714|||YM-222714；YM 222714|||YM222714|||YM-222714
Darexaban glucuronide is the major component in plasma after oral administration of darexaban to humans. Darexaban (YM150) is a direct inhibitor of factor Xa.
价 格：￥电议型 号：T27121产 地：中国大陆
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T2712Nifekalant hydrochloride；盐酸尼非卡兰Nifekalant hydrochloride
Nifekalant hydrochloride is an IKr potassium channel blocker with an IC50 of 10 ?M. It is a Class III antiarrhythmic compound and can be used in the study of tachyarrhythmias.
价 格：￥电议型 号：T2712产 地：中国大陆
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T27119L(Rac)-Daglutril；化合物(Rac)-DaglutrilSLV 306 acetic acid|||2-((3S)-3-(1-(2-(ethoxycarbonyl)-4-phenylbut
(Rac)-Daglutril (SLV 306 acetic acid) is the racemate form of Daglutril. Daglutril is an orally active, mixed neutral endopeptidase/endothelin converting enzyme inhibitor under development for the treatment of essential hypertension and congestive heart failure.
价 格：￥电议型 号：T27119L产 地：中国大陆
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T27119Daglutril；化合物 T27119SLV306|||SLV 306|||SLV-306；SLV306|||SLV 306|||SLV-306
Daglutril, a NEP/ECE inhibitor, is potentially used for the treatment of hypertension, heart failure andpulmonary. Daglutril inhibits systemic conversion of big endothelin-1 in humans.
价 格：￥电议型 号：T27119产 地：中国大陆
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T27118DAA-1097；化合物 T27118DAA-1097
DAA-1097 is a novel ligand of peripheral benzodiazepine receptor.
价 格：￥电议型 号：T27118产 地：中国大陆
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T27117DA-6886；化合物DA-6886DA6886|||DA 6886；DA6886|||DA 6886
DA-6886 is an agonist 5-Hydroxytryptamine receptor 4 (5-HT4). DA-6886 induced relaxation of the rat oesophagus preparation in a 5-HT4 receptor antagonist-sensitive manner. The evaluation of DA-6886 in CHO cells expressing hERG channels revealed that it inhibited hERG channel current with an pIC50 value of 4.3, indicating that the compound was 1000-fold more selective for the 5-HT4 receptor over hERG channels.
价 格：￥电议型 号：T27117产 地：中国大陆
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T27115CZh226；化合物 T27115CZh-226|||CZh 226；CZh-226|||CZh 226
CZh226 is a potent and selective PAK4 inhibitor (PAK4 Ki = 9 nM; PAK1 Ki = 3112 nM). CZh226 potently inhibits the migration and invasion of A549 tumor cells by regulating the PAK4-directed downstream signaling pathways in vitro.
价 格：￥电议型 号：T27115产 地：中国大陆
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T27114CZC-13788；化合物 T27114CZC13788|||CZC 13788；CZC13788|||CZC 13788
CZC-13788 is a highly potent and selective H4R antagonist with the potential utility in the treatment of inflammatory diseases.
价 格：￥电议型 号：T27114产 地：中国大陆
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T27113Camptothecin-20(S)-O-propionate；化合物 T27113CZ 48|||CZ48|||CZ-48；CZ 48|||CZ48|||CZ-48
CZ-48 is a DNA topoisomerase inhibitor.
价 格：￥电议型 号：T27113产 地：中国大陆
