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T63443XR8-89；化合物 XR8-89XR8-89
XR8-89, a potent inhibitor of papain-like protease (PLpro), exhibits an IC50 value of 0.1 μM and effectively hinders SARS-CoV-2 replication by inducing conformational changes in the SARS-COV-2 papain-like protease. This compound holds potential for SARS-CoV-2 research applications [1].
价 格：￥电议型 号：T63443产 地：中国大陆
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T63442DNA Gyrase-IN-2；化合物 DNA Gyrase-IN-2DNA Gyrase-IN-2
DNA Gyrase-IN-2 is a bacterial DNA cyclooxygenase B inhibitor that acts on Escherichia coli DNA cyclooxygenase (IC50: 3.29-10.49 μM) and Mycobacterium tuberculosis DNA cyclooxygenase (IC50: 4.41-5.61 μM), exhibiting antibacterial and antitubercular effects.
价 格：￥电议型 号：T63442产 地：中国大陆
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T63441HER2-IN-6；化合物 HER2-IN-6HER2-IN-6
HER2-IN-6 is a potent inhibitor of HER2. HER2-IN-6 has the potential to be investigated in wild and/or mutant EGFR and/or HER2 kinase-mediated tumors.
价 格：￥电议型 号：T63441产 地：中国大陆
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T63440Dyrk1A-IN-2；化合物 Dyrk1A-IN-2Dyrk1A-IN-2
Dyrk1A-IN-2 is a DYRK1A inhibitor (EC50: 37 nM). dyrk1A-IN-2 exhibits efficient promotion of human β-cell replication, as well as low cytotoxicity.
价 格：￥电议型 号：T63440产 地：中国大陆
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T6344Sevelamer hydrochloride；化合物Sevelamer HClSevelamer HCl；Sevelamer HCl
Sevelamer hydrochloride (Sevelamer HCl) is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.
价 格：￥电议型 号：T6344产 地：中国大陆
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T63344Lp-PLA2-IN-4；化合物 Lp-PLA2-IN-4Lp-PLA2-IN-4
Lp-PLA2-IN-4 is a potent lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor. Lp-PLA2-IN-4 has the potential to be studied in diseases associated with Lp-PLA2 activity, such as Alzheimer´s disease, atherosclerosis, and is an inhibitor of platelet-activating factor acetylhydrolase (PAF-AH), a phospholipase A2 involved in lipoprotein lipid or phospholipid hydrolysis. Compound 38).
价 格：￥电议型 号：T63344产 地：中国大陆
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T62344MIF-IN-3；化合物 MIF-IN-3MIF-IN-3
MIF-IN-3 is an inhibitor of migration inhibitory factor (MIF), which can be used in the study of immunoinflammation-related diseases.
价 格：￥电议型 号：T62344产 地：中国大陆
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T61344VO-OHPic；化合物 VO-OHPicVO-OHPic
VO-OHPic is a reversible, noncompetitive, and selective inhibitor of PTEN with an IC50 of 46 nM. It effectively attenuates apoptosis, adverse cardiac remodeling, and the presence of pro-inflammatory M1 macrophages in models of doxorubicin-induced cardiomyopathy. Additionally, VO-OHPic inhibits autophagy [1] [2] [3].
价 格：￥电议型 号：T61344产 地：中国大陆
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T60344L-Cytidine；化合物 L-CytidineL-Cytidine
L-Cytidine is an L-configurational form of Cytidine. L-Cytidine is a pyrimidine nucleoside which is a component of RNA. Cytidine can control the glial glutamate cycle, and affect brain phospholipid metabolism, catecholamine synthesis and mitochondrial function [1] [2].
价 格：￥电议型 号：T60344产 地：中国大陆
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T5344SP-420；化合物SP-420SP 420；SP 420
SP-420 is a novel orally active iron chelator.
价 格：￥电议型 号：T5344产 地：中国大陆
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T4344ALW-II-41-27；化合物ALW-II-41-27Eph receptor tyrosine kinase inhibitor；Eph receptor tyrosine kinase inhi
ALW-II-41-27 (Eph receptor tyrosine kinase inhibitor), an Eph receptor tyrosine kinase inhibitor, is used for cancer therapy.
价 格：￥电议型 号：T4344产 地：中国大陆
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T41295LY 344864 hydrochloride；化合物 LY 344864 hydrochlorideLY 344864 hydrochloride
LY 344864 hydrochloride is a selective receptor agonist with an affinity of 6 nM (Ki) at the 5-HT1F receptor.
价 格：￥电议型 号：T41295产 地：中国大陆
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T40428LTfR-T12 acetate；化合物TfR-T12 acetateTfR-T12 acetate (344618-30-0 Free base)；TfR-T12 acetate (344618-30
TfR-T12 acetate is a peptide binding to the transferrin receptor (TfR) and is subsequently internalized into TfR-expressing cells.
价 格：￥电议型 号：T40428L产 地：中国大陆
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T40344CBP/p300-IN-14CBP/p300-IN-14CBP/p300-IN-14
CBP/p300-IN-14, efficiently inhibits CBP/EP300 (lysine acetyltransferase) with an IC50 value of 3.3 nM.
价 格：￥电议型 号：T40344产 地：中国大陆
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T3S2344β,β-Dimethylacrylshikonin；β,β-二甲基丙烯酰紫草素Dimethylacrylshikonin|||β, β-Dimethylacrylshikonin；β,β-二甲基丙烯酰
1. β,β-Dimethylacrylshikonin (Dimethylacrylshikonin) is a promising agent for developing an improved strategy for radiotherapy against tumors. (a) Injection of Dimethylacrylshikonin combined with IR treatment significantly suppressed tumor growth of the HCT-116 xenograft. (b) Dimethylacrylshikonin significantly suppressed the growth of H(22) transplantable hepatoma, and induced the activation of caspase-3 . (c) Dimethylacrylshikonin inhibited growth of gastric cancer SGC-791 cells by inducing ER
价 格：￥电议型 号：T3S2344产 地：中国大陆
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T39344Z-VDVA-(DL-Asp)-FMK；Z-VDVA-(DL-Asp)-FMKZ-VDVA-(DL-Asp)-FMK
Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2.
价 格：￥电议型 号：T39344产 地：中国大陆
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T38995Taletrectinib free base；他雷替尼游离碱AB-106freebase|||Taletrectinib free base|||IBI-344 free base|||DS-605
Taletrectinib free base (AB-106 free base) is a novel potent, selective and orally active ROS1/NTRK inhibitor.Taletrectinib free base has potent inhibitory effects on recombinant ROS1, NTRK1, NTRK2, and NTRK3, with IC50s of 0.207, 0.622, 2.28 and 0.98 nM, respectively, Taletrectinib free base also inhibited ROS1 G2032R and other Crizotinib-resistant ROS1 mutations.
价 格：￥电议型 号：T38995产 地：中国大陆
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T38344Lalistat 1；化合物Lalistat 1ZINC795230；ZINC795230
Lalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae. Lalistat 1 can be used in studies about niemann-pick type C diseases.
价 格：￥电议型 号：T38344产 地：中国大陆
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T373445,6-dimethyl-2-Thiouracil；5,6-dimethyl-2-Thiouracil5,6-dimethyl-2-Thiouracil
5,6-dimethyl-2-Thiouracil is a heterocyclic building block that has been used in the synthesis of anti-HIV-1 pyrimidinones.1 It has also been used as an internal standard for the quantification of thyreostats, including 2-thiouracil, in bovine plasma.2
价 格：￥电议型 号：T37344产 地：中国大陆
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T36344Ac-LEVD-AFC；Ac-LEVD-AFCAc-LEVD-AFC
Ac-LEVD-AFC has a wide range of applications in life science related research.
价 格：￥电议型 号：T36344产 地：中国大陆
