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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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T9127MYLS22OPA1,Inhibitor,MYLS22,optic,atrophy,endothelial,MYLS-22,inhibit,MYLS 22,tumor
MYLS22 is a first-in-class and selective inhibitor of optic atrophy 1 (OPA1) . MYLS22 can target endothelial OPA1 to curtail tumor growth and inhibits angiogenesis by impinging on NFkB activity and on angiogenic gene expression. It with anti-angiogenesis and anti-cancer activity.
价 格：￥电议型 号：T9127产 地：中国大陆
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TN1096Ginsenoside Ra1Ginsenoside Ra1,inhibit,Inhibitor,Ginsenoside Ra 1,Ginsenoside Ra-1
Ginsenoside Ra1 is a component from ginseng. Ginsenoside Ra1 shows significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R).
价 格：￥电议型 号：TN1096产 地：中国大陆
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T6875LesinuradRDEA 594,RDEA-594,SLC22A12,Inhibitor,Lesinurad,inhibit,URAT1,Urate transporter 1
Lesinurad is a selective inhibitor of uric acid reabsorption which is used in combination with other agents in the therapy of gout. Lesinurad has had a limited clinical use but has not been associated with serum enzyme elevations during therapy or with instances of clinically apparent liver injury.
价 格：￥电议型 号：T6875产 地：中国大陆
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T9565OSBPL7-IN-1OSBPL7,orally active,ABCA1,OSBPL7 IN 1,Inhibitor,OSBPL-7-IN-1,OSBPL7IN1,inhibit
OSBPL7-IN-1 is an orally active inhibitor of oxysterol binding protein like 7 (OSBPL7). OSBPL7-IN-1 promotes an increase of ABCA1 at the plasma membrane without affecting mRNA expression[1].
价 格：￥电议型 号：T9565产 地：中国大陆
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T9009ICA-105574activator,KcsA,current amplitudes,ICA105574,ICA-105574,ICA 105574,Potassium Channel,inhibi
ICA-105574 is an activator of hERG that binds to the channel to remove inactivation, thus increasing peak current amplitude and shortening the action potential. It also modulates activation kinetics of the channel.
价 格：￥电议型 号：T9009产 地：中国大陆
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T7090Jionoside A1Inhibitor,Jionoside A-1,Jionoside A1,inhibit,Jionoside A 1
Jionoside A1 is isolated and purified from the roots of Rehmannia glutinosa. It displays dose-dependent immune-enhancement activity and possesses moderate neuroprotective activities on H2O2-treated SH-SY5Y cells.
价 格：￥电议型 号：T7090产 地：中国大陆
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T7131Antineoplaston A10Inhibitor,Antineoplaston A10,inhibit,Ras,Endogenous Metabolite,Antineoplaston A-10
Antineoplaston A 10 is a Ras inhibitor potentially for the treatment of glioma, lymphoma, astrocytoma and breast cancer.
价 格：￥电议型 号：T7131产 地：中国大陆
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T22789FPR A14FPR A-14,FPR A14
FPR A14 is an agonist of formyl peptide receptor (FPR) and induces cell differentiation.
价 格：￥电议型 号：T22789产 地：中国大陆
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T67756ISRIB-A15
ISRIB-A15 is an potent inhibitor of the integrated stress response with an EC50 of 0.8 nM.
价 格：￥电议型 号：T67756产 地：中国大陆
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T6217LFM-A13
LFM-A13（IC50=2.5 μM）, a specific Bruton´s tyrosine kinase (BTK), is more than 100-fold specificity than other protein kinases, such as JAK1, JAK2, HCK, EGFR, and IRK.
价 格：￥电议型 号：T6217产 地：中国大陆
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T5S2139Epimedin A1朝藿定A1；Hexandraside F
Epimedin A1(Hexandraside F) is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.
价 格：￥电议型 号：T5S2139产 地：中国大陆
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T5442A1874
A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degradation in cells. Effective in inhibiting many cancer cell lines proliferation.
价 格：￥电议型 号：T5442产 地：中国大陆
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T5379(Rac)-Antineoplaston A103-苯基乙酰氨基-2,6-哌啶二酮；Antineoplaston A10
(Rac)-Antineoplaston A10 is a naturally occurring substance and the first antineoplaston in the human body to be chemically identified. It displayed anti-proliferative action inhibiting cell growth.
价 格：￥电议型 号：T5379产 地：中国大陆
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T5330FluralanerAH252723；A1443；氟雷拉纳
Fluralaner is an isoxazoline ectoparasiticide. It potently and selectively inhibits binding of the GABA receptor channel blocker EBOB to housefly head membranes (IC50: 455 pM).
价 格：￥电议型 号：T5330产 地：中国大陆
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T5315TCA1TCA 1；TCA-1
TCA-1 is a small molecule with activity against drug-resistant and persistent tuberculosis.
价 格：￥电议型 号：T5315产 地：中国大陆
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T5104BTSA1
BTSA1 is a BAX activator that binds with high affinity and specificity to the N-terminal activation site and induces conformational changes to BAX leading to BAX-mediated apoptosis.
价 格：￥电议型 号：T5104产 地：中国大陆
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T5037Midecamycin麦迪霉素；Turimycin P3；Medecamycin A1；Espinomycin A；Platenomycin B1；Rubimycin；Antibiotic SF-83
Midecamycin, an acetoxy-substituted macrolide antibiotic, has effective on gram-positive and gram-negative bacteria acts by inhibiting bacterial protein synthesis.
价 格：￥电议型 号：T5037产 地：中国大陆
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T4343A-196A196；A 196
A-196 is a potent and selective inhibitor of SUV420 h1 and SUV420 h2 with IC50 values of 0.025 and 0.144 μM, respectively; more than 100-fold selective over other histone methyltransferases and non-epigenetic targets.
价 格：￥电议型 号：T4343产 地：中国大陆
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T40437LCaloxin 2A1 acetate
Caloxin 2A1 acetate is an inhibitor of extracellular plasma membrane Ca2+-ATPase (PMCA) peptide. Caloxin 2A1 acetate inhibits Ca2+-dependent formation of the 140-kDa acid-stable acylphosphate.
价 格：￥电议型 号：T40437L产 地：中国大陆
