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TN7142N-methyl-1H-indole-2-carboxamide
Indole-2-carboxylic acid methylamide is a marine derived natural products found in Neosartorya pseudofischeri.
价 格：￥电议型 号：TN7142产 地：中国大陆
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T7142Cephalosporin C zinc saltInhibitor,Orthopoxvirus,Cephalosporin C zinc salt,Bacterial,inhibit,Cephalo
Cephalosporin C zinc salt was a potent inhibitor of SAMHD1 (IC50 : 1.1 ± 0.1 μM), and this inhibition was largely attributable to the presence of zinc.
价 格：￥电议型 号：T7142产 地：中国大陆
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T8738LUN42518 HCl 47142-51-8(free base)LUN-42518 HCl 47142-51-8(free base),LUN42518 HCl 47142 51 8(fre
LUN42518 HCl is an analogue of phentolamine. Phentolamine is a nonselective alpha-adrenergic antagonist.
价 格：￥电议型 号：T8738产 地：中国大陆
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TP1549LNY-BR-1 p904 A2 acetate(347142-73-8 free base)NY-BR-1 p-904 A2 acetate(347142-73-8 free base),NYBR1
T-cell clones specific for this NY-BR-1 epitope (p904) can recognize breast tumor cells expressing NY-BR-1.
价 格：￥电议型 号：TP1549L产 地：中国大陆
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T17142Toxoflavin毒黄素；Toxoflavine；PKF-118-310；Xanthothricin
Toxoflavin is an antagonist of transcription factor 4 (TCF4)/β-catenin complex. Toxoflavin also acts as an inhibitor of KDM4A.
价 格：￥电议型 号：T17142产 地：中国大陆
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T11277FG 7142ZK 39106；LSU-65
FG 7142 also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM). FG 7142 can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex. FG 7142 , a non-selectively benz
价 格：￥电议型 号：T11277产 地：中国大陆
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T11277FG 7142FG 7142,ZK 39106,LSU-65
?FG 7142??also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM).?FG 7142?can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex.?FG 7142 , a non-selectively be
价 格：￥电议型 号：T11277产 地：美洲
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T8738LUN42518 HCl 47142-51-8(free base)；化合物LUN42518 HClLUN42518 HCl 47142-51-8(free base)
LUN42518 HCl is an analogue of phentolamine. Phentolamine is a nonselective alpha-adrenergic antagonist.
价 格：￥电议型 号：T8738产 地：中国大陆
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T77142Ranevetmab；化合物 RanevetmabRanevetmab
Ranevetmab (NV-01), a caninized anti-nerve growth factor (anti-NGF) monoclonal antibody (mAb), is utilized in research for alleviating pain associated with degenerative joint disease (DJD) in canines.
价 格：￥电议型 号：T77142产 地：中国大陆
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T71429O-Demethyl apixaban sulfate；化合物 O-Demethyl apixaban sulfateO-Demethyl apixaban sulfate
O-Demethyl apixaban sulfate is a metabolite of Apixaban, a potent and highly selective factor Xa inhibitor. Apixaban is currently under development for treatment of arterial and venous thrombotic diseases.
价 格：￥电议型 号：T71429产 地：中国大陆
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T71428Mocoht bromide；化合物 Mocoht bromideMocoht bromide
Mocoht bromide is new antagonists of platelet activating factor.
价 格：￥电议型 号：T71428产 地：中国大陆
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T71427N-(5-((2-Methylene-3-(((octadecylamino)carbonyl)oxy)propoxy)carbonyl)pentyl)pyridinium；化合物 N-(5-((2-
N-(5-((2-Methylene-3-(((octadecylamino)carbonyl)oxy)propoxy)carbonyl)pentyl)pyridinium is a platelet activating factor antagonist.
价 格：￥电议型 号：T71427产 地：中国大陆
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T71426STA-1474；化合物 STA-1474STA-1474
STA-1474 is a water soluble prodrug of ganetespib (formerly STA-9090). STA-1474 will metabolized to Ganetespib, which is a potent HSP90 inhibitor previously shown to kill canine tumor cell lines in vitro and inhibit tumor growth in the setting of murine xenografts. The purpose of the following study was to extend these observations and investigate the safety and efficacy of STA-1474 in dogs with spontaneous tumors.
价 格：￥电议型 号：T71426产 地：中国大陆
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T71425Noberastine maleate；化合物 Noberastine maleateNoberastine maleate
Noberastine maleate, a histamine H1 antagonist, has potent and specific peripheral antihistaminic activity. Noberastine, a furan derivative of nor-astemizole (an astemizole metabolite), has been shown to have a more rapid onset, and shorter duration of action than astemizole with peak antihistaminic activity at 4h following ingestion. Noberastine is rapidly absorbed and the peak plasma levels are obtained within 2 h of oral dosing. In preclinical studies Noberastine has been shown to lack centra
价 格：￥电议型 号：T71425产 地：中国大陆
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T71424VT-102 free base；化合物 VT-102 free baseVT-102 free base
VT-102 is a TEAD Auto-palmitoylation inhibitor that Selectively Inhibit Proliferation and Tumor Growth of NF2-deficient Mesothelioma. VT102 inhibited the firefly luciferase reporter dose-dependently and had no 204 effect on the Renilla luciferase reporter.
价 格：￥电议型 号：T71424产 地：中国大陆
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T71423AZD5213；化合物 AZD-5213AZD5213
AZD5213 is a selective, competitive antagonist of the human H3 receptor, exhibiting a pK i of 9.3 against hH3R. It is utilized in the research of sleep and cognitive regulation.
价 格：￥电议型 号：T71423产 地：中国大陆
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T71422S6821；化合物 S6821S6821
S6821 is a TAS2R8 antagonist. S6821 was not found to be mutagenic or clastogenic in vitro, and did not induce micronuclei in bone marrow polychromatic erythrocytes in vivo.
价 格：￥电议型 号：T71422产 地：中国大陆
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T71421Bemoradan；化合物 BemoradanBemoradan
Bemoradan is an inhibitor of the rolipram-insensitive cyclic AMP phosphodiesterase from canine heart tissue
价 格：￥电议型 号：T71421产 地：中国大陆
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T71420RO314724；化合物 RO314724RO314724
RO314724 is a HDAC inhibitor. RO314724 is also a a reversible, tightly binding, MMP inhibitor with a Ki of 26 nm. Matrix metalloproteinases (MMPs) belong to the key enzymes of the proteolytic destruction of cartilage matrix during chronic rheumatic diseases. Ro314724 displayed MMP-proteoglycanase inhibitory activity both in vitro and ex vivo and proved to be not harmful to the morphology, viability and proteoglycan biosynthesis of bovine articular cartilage explants.
价 格：￥电议型 号：T71420产 地：中国大陆
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T7142Cephalosporin C zinc salt；头孢菌素C锌盐Cephalosporin C zinc salt
Cephalosporin C zinc salt was a potent inhibitor of SAMHD1 (IC50 : 1.1 ± 0.1 μM), and this inhibition was largely attributable to the presence of zinc.
价 格：￥电议型 号：T7142产 地：中国大陆
