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T68159Tetrazolast；四唑司特Tetrazolast
Tetrazolast has anticancer activity and may have antifungal activity.
价 格：￥电议型 号：T68159产 地：中国大陆
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T6715912-(1-Pyrenyl)dodecanoic acid；化合物 12-(1-Pyrenyl)dodecanoic acid12-(1-Pyrenyl)dodecanoic acid
12-(1-Pyrenyl)dodecanoic acid is a useful organic compound for research related to life sciences. The catalog number is T67159 and the CAS number is 69168-45-2.
价 格：￥电议型 号：T67159产 地：中国大陆
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T65159Ethyl 2-oxo-2-(thiophen-2-yl)acetate；化合物 Ethyl 2-oxo-2-(thiophen-2-yl)acetateEthyl 2-oxo-2-(thiophen
Ethyl 2-oxo-2-(thiophen-2-yl)acetate is a useful organic compound for research related to life sciences. The catalog number is T65159 and the CAS number is 4075-58-5.
价 格：￥电议型 号：T65159产 地：中国大陆
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T64159Cathepsin K inhibitor 2；化合物 Cathepsin K inhibitor 2Cathepsin K inhibitor 2
Cathepsin K inhibitor 2 is a potent inhibitor of cathepsin K. Cathepsin K (Cat K) is a cysteine protease expressed under the control of the CTSK gene, which is closely related to osteoporosis and hydrolyses collagen. cathepsin K inhibitor 2 has shown potential in osteoarthritis.
价 格：￥电议型 号：T64159产 地：中国大陆
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T64127VT-1598；化合物 VT-1598VT-1598
VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.
价 格：￥电议型 号：T64127产 地：中国大陆
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T6367Abacavir sulfate；硫酸阿巴卡韦Abacavir Hemisulfate|||1592U89|||ABC sulfate|||Ziagen；Abacavir Hemisulfate|||
Abacavir sulfate (Ziagen) , a nucleoside analogue, effectively utilize its antiviral activity
价 格：￥电议型 号：T6367产 地：中国大陆
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T63159Anticancer agent 28；化合物 Anticancer agent 28Anticancer agent 28
Anticancer agent 28 showed good anti-tumour effects in vivo in H22 allograft mice. anticancer agent 28 was 50 times more potent than Oridonin against K562 cells with an IC50 value of 0.09 μM.
价 格：￥电议型 号：T63159产 地：中国大陆
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T62159Antifungal agent 24；化合物 Antifungal agent 24Antifungal agent 24
Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).
价 格：￥电议型 号：T62159产 地：中国大陆
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T6214Emtricitabine恩曲他滨恩曲他滨|||FTC|||Emtriva|||BW1592
Emtricitabine (FTC) (FTC), a nucleoside reverse transcriptase inhibitor, exhibits inhibition activity against human immunodeficiency virus (HIV) and hepatitis B virus.
价 格：￥电议型 号：T6214产 地：中国大陆
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T61933MK-0159；化合物 MK-0159MK-0159
MK-0159 is an orally available, highly potent CD38 inhibitor with myocardial injury protection for the study of cardiac ischemia and reperfusion injury.
价 格：￥电议型 号：T61933产 地：中国大陆
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T61599XT2；化合物 XT2XT2
XT2 is a highly potent, orally active, and selective inhibitor of NF-κB-inducing kinase (NIK), exhibiting an IC50 of 9.1 nM. It effectively suppresses the upregulation of ALT, a vital biomarker for acute liver injury, induced by CCl4. Additionally, XT2 significantly decreases immune cell infiltration into the damaged liver tissue. As a result, XT2 holds immense potential in liver inflammatory disease research [1].
价 格：￥电议型 号：T61599产 地：中国大陆
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T61598Polyketide synthase 13-IN-2；化合物 Polyketide synthase 13-IN-2Polyketide synthase 13-IN-2
Polyketide synthase 13-IN-2 (comp 42) is a potent inhibitor of polyketide synthase 13 in Mycobacterium tuberculosis. It demonstrates a minimum inhibitory concentration (MIC) of 0.25 μg/mL [1].
价 格：￥电议型 号：T61598产 地：中国大陆
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T61597Nampt-IN-7；化合物 Nampt-IN-7Nampt-IN-7
Nampt-IN-7, also known as compound GF8, is a powerful NAMPT inhibitor exhibiting an IC50 value of 7.31 μM. It possesses significant cytotoxic effects against the human HepG2 hepatocellular carcinoma cell line, with an IC50 value of 24.28 μM [1].
价 格：￥电议型 号：T61597产 地：中国大陆
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T61596EGFR/HER2/DHFR-IN-1；化合物 EGFR/HER2/DHFR-IN-1EGFR/HER2/DHFR-IN-1
EGFR/HER2/DHFR-IN-1 is a highly selective and potent anticancer compound specifically targeting MCF-7 breast cancer cells. It acts as a multi-inhibitor, targeting the EGFR/HER2 kinase and DHFR enzymes, with IC50 values of 0.153 μM, 0.108 μM, and 0.291 μM, respectively. Its mechanism of action involves cell cycle arrest at the G1/S phase and induction of apoptosis in cells [1].
价 格：￥电议型 号：T61596产 地：中国大陆
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T61595Antitubercular agent-12；化合物 Antitubercular agent-12Antitubercular agent-12
Antitubercular agent-12 (Compound 2c) is a highly effective antitubercular agent, with a MIC (Minimum Inhibitory Concentration) value of 1.439 μg/mL. Notably, Antitubercular agent-12 exhibits significantly reduced cytotoxicity, reflected by a CC50 (50% Cytotoxic Concentration) value of 57.34 μg/mL [1].
价 格：￥电议型 号：T61595产 地：中国大陆
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T61594BF844；化合物 BF844BF844
BF844 is a chemical compound that demonstrates the ability to mitigate hearing loss in individuals with Usher Syndrome Type III (USH3) caused by the CLRN1 mutation (specifically N48K). One of its mechanisms of action is the transportation of CLRN1 N48K to the plasma membrane. In vivo studies have shown that BF844 significantly preserves hearing [1].
价 格：￥电议型 号：T61594产 地：中国大陆
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T6159311β-HSD1-IN-6；化合物 11β-HSD1-IN-611β-HSD1-IN-6
11β-HSD1-IN-6 is a potent inhibitor of 11β hydroxysteroid dehydrogenase enzymes (11β-HSDs). These enzymes are responsible for catalyzing the conversion of the active glucocorticoids, corticosterone or cortisol, to their respective inactive forms, 11-dehydrocorticosterone (11-DHC) and cortisone. The compound 11β-HSD1-IN-6 specifically targets and inhibits 11β-HSD-1, effectively modulating the interconversion of these glucocorticoids. [1]
价 格：￥电议型 号：T61593产 地：中国大陆
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T61592Thalidomide-piperazine hydrochloride；化合物 Thalidomide-piperazine hydrochlorideThalidomide-piperazine
Thalidomide-piperazine hydrochloride is a chemical compound with potential applications in the research of leprosy and multiple myeloma. It serves as a valuable tool in developmental biology, facilitating significant discoveries in the biochemical pathways of limb development [1].
价 格：￥电议型 号：T61592产 地：中国大陆
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T61591SARS-CoV-2-IN-20；化合物 SARS-CoV-2-IN-20SARS-CoV-2-IN-20
SARS-CoV-2-IN-20 (Compound 1a) is a highly effective inhibitor of SARS-CoV-2, displaying an impressive EC50 value of 6.5 μM. With its exceptional inhibitory properties, SARS-CoV-2-IN-20 holds great potential for advancing research on infectious diseases [1].
价 格：￥电议型 号：T61591产 地：中国大陆
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T61590DS96432529；化合物 DS96432529DS96432529
DS96432529 is a potent and orally active bone anabolic agent through CDK8 inhibition.
价 格：￥电议型 号：T61590产 地：中国大陆
