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T23949Dacemazine hydrochloride；化合物 T23949Ahistan HCl|||Dacemazine HCl|||Histantine HCl|||UNII-DK78VKA001；A
Dacemazine is a phenothiazine derivative that acts as a histamine antagonist at the H1 subtype. It was also assessed as a possible anticancer drug.
价 格：￥电议型 号：T23949产 地：中国大陆
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T23947DA-7867；化合物 T23947UNII-491MT9GU8K|||DA 7867|||DA7867；UNII-491MT9GU8K|||DA 7867|||DA7867
DA-7867 is a novel oxazolidinone. DA-7867 had the lowest MIC for 90% of the aerobic gram-positive bacterial strains tested (≤0.25 μg/ml) and it was more potent than linezolid. DA-7867 was the most active drug with a MIC(90) of 0.125 μg/ml.
价 格：￥电议型 号：T23947产 地：中国大陆
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T23946DA-3934；化合物 T23946UNII-J353803KRG；UNII-J353803KRG
DA-3934 has a high affinity for gastrin/CCK-B receptors and high selectivity over CCK-A receptors. DA-3934 and its methyl ester derivative inhibited pentagastrin-induced gastric acid secretion in rats in a dose-dependent manner.
价 格：￥电议型 号：T23946产 地：中国大陆
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T23945DA-11004；化合物 T23945DA11004|||UNII-48M66E9ER2；DA11004|||UNII-48M66E9ER2
DA-11004 is a potent NADP-dependent isocitrate dehydrogenase inhibitor (IC50: 1.49 μM for IDPc). DA-11004 inhibited fatty acid synthesis in adipose tissues via IDPc inhibition. It also decreased the plasma glucose levels and FFA in HF diet-induced obesity of C57BL/6J mice.
价 格：￥电议型 号：T23945产 地：中国大陆
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T23881Wee1 Inhibitor II；化合物 T23881Wee1-Inhibitor II|||Wee1-Inhibitor-II|||Wee1 Inhibitor-II；Wee1-Inhibitor
Wee1 Inhibitor II is an ATP-binding site-targeting Wee1 inhibitor.
价 格：￥电议型 号：T23881产 地：中国大陆
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T23790BIIB-057；化合物 T23790BIIB 057；BIIB 057
BIIB-057 is a selective Syk inhibitor.
价 格：￥电议型 号：T23790产 地：中国大陆
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T2373Vipadenant；化合物VipadenantCEB-4520|||BIIB-014；CEB-4520|||BIIB-014
Vipadenant (CEB-4520)(BIIB-014) is an adenosine A2a antagonist with Ki of 1.3 nM; less potent for A1(Ki=69 nM).
价 格：￥电议型 号：T2373产 地：中国大陆
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T23504VEGFR-IN-1化合物 T23504VEGFR Tyrosine Kinase Inhibitor II
VEGFR inhibitor
价 格：￥电议型 号：T23504产 地：中国大陆
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T23295(S)-(-)-5-Iodowillardiine化合物 T23295(S)()5Iodowillardiine|||(S) ( ) 5 Iodowillardiine
hGluR5 kainate receptor agonist
价 格：￥电议型 号：T23295产 地：中国大陆
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T22980MIRA-1；化合物MIRA-1p53 Activator VIII|||1-[(1-Oxopropoxy)methyl]-1H-pyrrole-2,5-dione|||(2,5-dioxo-2,5-
MIRA-1 (WRN Helicase Inhibitor) is a restorer of wild-type p53 conformation/cellular function and selectively inhibits Werner syndrome WRN helicase activity with an IC50 of 20 ?M.
价 格：￥电议型 号：T22980产 地：中国大陆
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T2286BIIB021；化合物BIIB-021BIIB 021|||CNF2024|||BIIB-021；BIIB 021|||CNF2024|||BIIB-021
BIIB021 (CNF2024) is an orally-available, fully synthetic inhibitor of HSP90(Ki=1.7 nM, EC50=38 nM).
价 格：￥电议型 号：T2286产 地：中国大陆
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T22659Chlorisondamine diiodide化合物 T22659Chlorisondamine diiodide
long lasting nicotinic antagonist
价 格：￥电议型 号：T22659产 地：中国大陆
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T22607Bisindolylmaleimide II；化合物 T22607Bisindolylmaleimide II
protein kinase C (PKC) inhibitor
价 格：￥电议型 号：T22607产 地：中国大陆
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T22560ALK5 Inhibitor II (hydrochloride)；化合物 T22560ALK5 Inhibitor II (hydrochloride)
ALK5 Inhibitor II is an ALK5 inhibitor. IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-β cellular assay, and ALK5 binding in HepG2 cells, respectively.
价 格：￥电议型 号：T22560产 地：中国大陆
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T22353Lanthanum(III) chloride heptahydrate；氯化镧(III)七水合物Lanthanum(III) chloride heptahydrate
Lanthanum(III) chloride is an inorganic compound which used in biochemical research to block the activity of divalent cation channels, especially calcium channels.
价 格：￥电议型 号：T22353产 地：中国大陆
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T2217Cephalomannine；三尖杉宁碱Baccatin III；Baccatin III|||三尖杉宁碱
Cephalomannine (Baccatin III) is a taxol derivative obtained from Taxus yunnanensis with antitumor activity.
价 格：￥电议型 号：T2217产 地：中国大陆
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T22115SM-7368；化合物NF-κB Activation Inhibitor IIISM-7368
The NF-κB Activation Inhibitor III, controls the biological activity of NF-κB. It is primarily used for Inflammation/Immunology applications.
价 格：￥电议型 号：T22115产 地：中国大陆
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T22021ACHP；化合物ACHPIKK-2 Inhibitor VIII；IKK-2 Inhibitor VIII
ACHP (IKK-2 Inhibitor VIII) is a novel selective and potent IKK inhibitor with inhibitory effects on IKK-α and IKK-β. ACHP has anti-HIV-1 activity and inhibits HIV-1 long terminal repeat (LTR)-driven gene expression through inhibition of NF-κB activation, inhibits TNF-α-induced NF-κB (p65) recruitment to the HIV-1 LTR, and inhibits TNF-α-induced NF-κB (p65) recruitment to the HIV-1 LTR. ACHKP has anti-HIV-1 activity and inhibits TNF-α-induced recruitment of NF-κB (p65) to the HIV-1 LTR.
价 格：￥电议型 号：T22021产 地：中国大陆
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T219710-Deacetylbaccatin III10-脱乙酰巴卡丁 III10-脱乙酰巴卡丁 III|||10-脱乙酰基巴卡丁III
10-Deacetylbaccatin-III is an intermediate for taxol analog preparations with anti-cancer activity.
价 格：￥电议型 号：T2197产 地：中国大陆
