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T71172U 80215；化合物 U 80215U 80215
U 80215 is an enzyme-competitive inhibitor.
价 格：￥电议型 号：T71172产 地：中国大陆
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T70756KT172；化合物 KT172KT172
KT172, a DAGLβ inhibitor, exhibits an IC50 value of 11 nM and has applications in metabolic and inflammatory research.
价 格：￥电议型 号：T70756产 地：中国大陆
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T70172NY0173；化合物 NY0173NY0173
NY0173 is a potent exchange protein activated by cAMP antagonists.
价 格：￥电议型 号：T70172产 地：中国大陆
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T69508GRL-1720；化合物 GRL-1720GRL-1720
GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro)
价 格：￥电议型 号：T69508产 地：中国大陆
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T69450DU172；化合物 DU172DU172
DU172 is the tyrosine-targeted covalent adenosine A1 receptor antagonist.
价 格：￥电议型 号：T69450产 地：中国大陆
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T69172Acetomycin；化合物 AcetomycinAcetomycin
Acetomycin is a γ-lactone microbial metabolite originally isolated from S. ramulosus that has anticancer activity. It inhibits proliferation of HCT-8 human colon and L1210 mouse leukemia cancer cells.
价 格：￥电议型 号：T69172产 地：中国大陆
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T68172Zalospirone；扎螺酮Zalospirone
Zalospirone is a 5-HT1A receptor agonist that can be used to study anxiety disorders and major depressive disorder.
价 格：￥电议型 号：T68172产 地：中国大陆
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T671722-(4-Chlorophenyl)quinoline-4-carboxylic acid；化合物 2-(4-Chlorophenyl)quinoline-4-carboxylic acid2-(4-
2-(4-Chlorophenyl)quinoline-4-carboxylic acid is a useful organic compound for research related to life sciences. The catalog number is T67172 and the CAS number is 5466-31-9.
价 格：￥电议型 号：T67172产 地：中国大陆
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T66172N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butylthio)-L-cysteine；化合物 N-(((9H-Fluoren-9-yl)methox
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butylthio)-L-cysteine is a useful organic compound for research related to life sciences. The catalog number is T66172 and the CAS number is 73724-43-3.
价 格：￥电议型 号：T66172产 地：中国大陆
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T65172Flavin adenine dinucleotide；黄素腺嘌呤二核苷酸FAD；FAD
Flavin adenine dinucleotide (FAD) is a REDOX cofactor, a protein cogroup, involved in a variety of metabolic reactions.
价 格：￥电议型 号：T65172产 地：中国大陆
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T64172MraY-IN-1；化合物 MraY-IN-1MraY-IN-1
MraY-IN-1 (compound 12a) is a potent inhibitor (IC50: 140 μM) of the bacterial translocase MraY. MraY-IN-1 has antibacterial activity against Escherichia coli K12 (MIC50: 7 μg/ml), Bacillus subtilis W23 (MIC50: 12 μg/ml) and Pseudomonas fluorescens Pf-5 (MIC50: 46 μg/ml). /MraY-IN-1 can be used for antimicrobial studies.
价 格：￥电议型 号：T64172产 地：中国大陆
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T63172LPA5 antagonist 2；化合物 LPA5 antagonist 2LPA5 antagonist 2
LPA5 antagonist 2 (compound 65) is a highly water-soluble LPA5 antagonist that significantly reduces nociception.LPA5 antagonist 2 can be used to study inflammatory and neuropathic pain.
价 格：￥电议型 号：T63172产 地：中国大陆
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T62172Dual AChE-MAO B-IN-1；化合物 Dual AChE-MAO B-IN-1Dual AChE-MAO B-IN-1
Dual AChE-MAO B-IN-1 (compound 15) is a safe, metabolically stable neuroprotective agent.Dual AChE-MAO B-IN-1 is a potent, orally active CNS-permeable inhibitor of human AChE (IC50=550 nM) and MAO-B (IC50=8.2 nM), and has low in vitro activity against AChE and MAO-B with IC50 values of 550 nM, 8.2 nM respectively.
价 格：￥电议型 号：T62172产 地：中国大陆
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T61729Terazosin；化合物 TerazosinTerazosin
Terazosin, a quinazoline derivative, is an orally active and competitive antagonist of α1-adrenoceptors. Its mechanism of action involves relaxing blood vessels and promoting bladder opening. Terazosin exhibits therapeutic potential for treating benign prostatic hyperplasia (BPH) and high blood pressure [1][2][3].
价 格：￥电议型 号：T61729产 地：中国大陆
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T61728MY-875；化合物 MY-875MY-875
MY-875 is a potent microtubulin polymerization inhibitor that competes at colchicine binding sites, exhibiting an IC50 value of 0.92 μM. It effectively suppresses microtubulin polymerization, exerting its inhibitory effect. Additionally, MY-875 exerts its biological impact by activating the Hippo pathway, inducing apoptosis, and displaying commendable anticancer activity [1].
价 格：￥电议型 号：T61728产 地：中国大陆
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T61727HDAC6/8/BRPF1-IN-1；化合物 HDAC6/8/BRPF1-IN-1HDAC6/8/BRPF1-IN-1
HDAC6/8/BRPF1-IN-1 is a dual inhibitor that targets HDAC6, HDAC8, and the bromodomain and PHD finger containing protein 1 (BRPF1). It exhibits inhibitory activity against HDAC1, HDAC6, and HDAC8 with IC50 values of 797 nM, 344 nM, and 908 nM, respectively. In addition, it inhibits BRPF1 with a Kd value of 175.2 nM. This compound is utilized in cancer research [1].
价 格：￥电议型 号：T61727产 地：中国大陆
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T617266BrCaQ；化合物 6BrCaQ6BrCaQ
6BrCaQ is a highly potent inhibitor of mitochondrial heat shock protein TRAP1, exhibiting significant antiproliferative properties. Additionally, 6BrCaQ can be utilized for the synthesis of 6BrCaQ-TPP conjugates [1].
价 格：￥电议型 号：T61726产 地：中国大陆
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T61725VU0463271 quarterhydrate；化合物 VU0463271 quarterhydrateVU0463271 quarterhydrate
VU0463271 quarterhydrate is a potent KCC2 antagonist, with an IC 50 of 61 nM [1].
价 格：￥电议型 号：T61725产 地：中国大陆
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T61724SB 258741 hydrochloride；化合物 SB 258741 hydrochlorideSB 258741 hydrochloride
SB 258741 hydrochloride is a potent antagonist of the 5-HT 7 receptor, designed specifically for studying schizophrenia [1].
价 格：￥电议型 号：T61724产 地：中国大陆
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T61723SS-RJW100；化合物 SS-RJW100SS-RJW100
SS-RJW100 is an enantiomer of RJW100, known as a racemic agonist that targets two nuclear receptors: liver receptor homolog 1 (LRH-1) and steroidogenic factor 1 (SF-1). In vitro experiments reveal that SS-RJW100 promotes the recruitment of coregulator protein fragments and enhances the interaction with the transcriptional intermediary factor 2 (Tif2) coactivator specifically for LRH-1. Additionally, SS-RJW100 disrupts the allosteric activation networks of LRH-1, displaying suboptimal thermal sta
价 格：￥电议型 号：T61723产 地：中国大陆
