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T8954ML179C57Bl6 mice,inhibit,SAA4,ER-negative breast cancer,probe compounds,ML 179,MCF-7,SAA1,Inhibitor,
ML179 is a potent and selective inverse agonist of liver receptor homolog-1 (LRH1, NR5A2) with IC50 of 320 nM.
价 格：￥电议型 号：T8954产 地：中国大陆
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T13101TC-MCH 7cTCMCH 7c,TC MCH 7c
TC-MCH 7c is an orally available, selective and brain-penetrable antagonist of MCH1R(IC50 of 5.6 nM for hMCH1R),and is a phenylpyridone derivative.
价 格：￥电议型 号：T13101产 地：中国大陆
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T9636DalpiciclibMCF7,BT-474/T,Cyclin dependent kinase,Eca 109,MCF7/TR,and KYSE-510 ESCC,SHR6390,Inhibitor
Dalpiciclib is a highly selective, orally bioavailable, and comparable potency inhibitor of CDK4 and CKD6 with IC50s of 12.4?nM and 9.9?nM, respectively. Dalpiciclib exerts potent antitumor activity in esophageal squamous cell carcinoma by inhibiting phosphorylated tumor suppressor retinoblastoma protein (Rb) and inducing G1 cell cycle arrest.
价 格：￥电议型 号：T9636产 地：中国大陆
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T8716physalin Fcytokine,PBMC,physalin F,HTLV-1,infection,inflammatory,Inhibitor,Apoptosis,immunomodulator
Physalin F is a natural blocker of CaV2.3 (R-type) and CaV2.2 (N-type) voltage-gated calcium channels.It is a secosteroid with potent anti-inflammatory and immunomodulatory activities. Physalin F induces apoptosis of PBMC, decreasing the spontaneous proliferation and cytokine production caused by Human T-lymphotropic virus type 1 (HTLV-1) infection
价 格：￥电议型 号：T8716产 地：中国大陆
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T8662UAMC-3203 hydrochlorideUAMC 3203 hydrochloride,UAMC3203,UAMC 3203,inhibit,UAMC-3203,Inhibitor,Ferrop
UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
价 格：￥电议型 号：T8662产 地：中国大陆
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TP1996MCH(human, mouse, rat)MCH(human, mouse, rat),inhibit,MCHR1 (GPR24),Inhibitor,Melanin concentrating h
Potent endogenous agonist at melanin-concentration hormone (MCH) receptors (IC50 values are 0.3 and 1.5 nM and EC50 values are 3.9 and 0.1 nM at MCH1 and MCH2 receptors respectively). Increases food intake in vivo.
价 格：￥电议型 号：TP1996产 地：中国大陆
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T8390CefazolinBacterial,Cefazolin,C8-B4,post-operative cognitive dysfunction,Antibiotic,PBMC,Inhibitor,an
Cefazolin is a semi-synthetic cephalosporin that has a broad spectrum of antibacterial activity and inhibits the synthesis of bacterial cell walls.
价 格：￥电议型 号：T8390产 地：中国大陆
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TN2252Syrosingopinecancer,Syrosingopine,NAD+,Su-3118,MCTs,Su 3118,synthetic lethality,inhibit,metformin,la
Syrosingopine has selective depleting effect on brain amines is potentiated by combined treatment with disulfiram or fusaric acid, a dopamine beta-hydroxylase inhibitor.
价 格：￥电议型 号：TN2252产 地：中国大陆
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T7294AramcholInhibitor,inhibit,Aramchol
Aramchol, also known as arachidyl amido cholanoic acid, is a conjugate of arachidic acid and cholic acid. It reduces ex vivo cholesterol crystallization in native human bile and dissolves pre-formed cholesterol crystals in a dose-dependent manner.
价 格：￥电议型 号：T7294产 地：中国大陆
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T9605Sangivamycincells,Nucleoside Antimetabolite/Analog,Sangivamycin,antitumor,NSC-65346,PKC,MCF7,NSC6534
Sangivamycin is an effective inhibitor of protein kinase C (PKC, Ki = 10 μM). Sangivamycin exhibits antiproliferative activity against a variety of human cancers.
价 格：￥电议型 号：T9605产 地：中国大陆
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T9122XL177AMCF7,XL177A,Deubiquitinase,inhibit,Inhibitor,cancer,XL-177A,DUBs,p53,USP7
XL177A is a selective irreversible USP7 inhibitor(IC50 : 0.34 nM). XL177A elicits cancer cell killing through a p53-dependent mechanism.
价 格：￥电议型 号：T9122产 地：中国大陆
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T6323Oligomycin AMCH 32；寡霉素A
Oligomycin A is an inhibitor of ATP synthase, inhibits oxidative phosphorylation and all the ATP-dependent processes occurring on the coupling membrane of mitochondria.
价 格：￥电议型 号：T6323产 地：中国大陆
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T6272Fosbretabulin DisodiumCA 4DP；Combretastatin A4 disodium phosphate；CA 4P；Fosbretabulin (Combretastati
Fosbretabulin (Combretastatin A4 Phosphate (CA4P)) Disodium, a water-soluble prodrug of Combretastatin A4 (CA4), is a microtubule-targeting agent that binds β-tubulin (Kd: 0.4 μM). Fosbretabulin Disodium inhibits the polymerization of tubulin (IC50: 2.4 μ
价 格：￥电议型 号：T6272产 地：中国大陆
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T6269BemcentinibBGB324；R428
R428 is a selective inhibitor of Axl (IC50: 14 nM) and has been investigated for the treatment of NSCLC.
价 格：￥电议型 号：T6269产 地：中国大陆
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T6069Gemcitabine hydrochlorideLY 188011 hydrochloride；LY188011；Gemzar；Gemcitabine HCl；吉西他滨盐酸盐；盐酸吉西他滨
Gemcitabine is a DNA synthesis inhibitor (IC50s: 12, 18, 40, 92.7, 89.3 in Capan2, BxPC-3, Mia Paca-2, PANC-1, and PL-45 cells, respectively).
价 格：￥电议型 号：T6069产 地：中国大陆
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T6057URMC-099URMC 099；URMC099
URMC-099 is an orally bioavailable, brain penetrant MLK inhibitor (IC50: 19/42/14/150 nM, for MLK1/MLK2/MLK3/DLK), and also inhibits LRRK2 activity (IC50: 11 nM).
价 格：￥电议型 号：T6057产 地：中国大陆
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T5823D-Lin-MC3-DMA
D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle.
价 格：￥电议型 号：T5823产 地：中国大陆
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T5814AurantiamideTMC-58B；橙黄胡椒酰胺
Aurantiamide has anti-cancer, anti-inflammatory and antinociceptive activities, it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the
价 格：￥电议型 号：T5814产 地：中国大陆
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T5533MC180295(rel)-MC180295
MC180295 is a novel potent, highly selective CDK9 inhibitor (IC50: 5 nM), displays >22-fold selectivity over other CDKs.
价 格：￥电议型 号：T5533产 地：中国大陆
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T5343UAMC-3203UAMC 3203；UAMC3203
UAMC-3203 is a potent and selective Ferroptosis inhibitor (IC50: 12 nM).
价 格：￥电议型 号：T5343产 地：中国大陆
