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T671681-(4-(Trifluoromethoxy)phenyl)thiourea；化合物 1-(4-(Trifluoromethoxy)phenyl)thiourea1-(4-(Trifluorometh
1-(4-(Trifluoromethoxy)phenyl)thiourea is a useful organic compound for research related to life sciences. The catalog number is T67168 and the CAS number is 142229-74-1.
价 格：￥电议型 号：T67168产 地：中国大陆
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T670771,3-diisopropylurea；化合物 1,3-diisopropylurea1,3-diisopropylurea
1,3-diisopropylurea is a useful organic compound for research related to life sciences and the catalog number is T67077.
价 格：￥电议型 号：T67077产 地：中国大陆
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T6636Refametinib；瑞法替尼//瑞美替尼BAY 86-97661|||BAY 869766|||RDEA119；BAY 86-97661|||瑞法替尼//瑞美替尼|||BAY 869766|||R
Refametinib (RDEA119) (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
价 格：￥电议型 号：T6636产 地：中国大陆
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T64357FA16；化合物FA16FA 16|||FA-16；FA 16|||FA-16
FA16 is a selective, metabolically stable ferroptosis inducer with an IC50 value of 1.26 μM.FA16 is a derivative of 2-(trifluoromethyl)benzimidazole.FA16 inhibits the cystine/glutamate inverse transporter protein (system Xc-)-mediated exchange of intracellular glutamate for extracellular cystine.FA16 significantly inhibited tumor growth in a HepG2 xenograft tumor model. HepG2 xenograft tumor model significantly inhibited tumor growth.
价 格：￥电议型 号：T64357产 地：中国大陆
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T64228ALDH1A1-IN-3；化合物 ALDH1A1-IN-3ALDH1A1-IN-3
ALDH1A1-IN-3 is a good and selective inhibitor of aldehyde dehydrogenase 1A1 (ALDH1A1) (IC50: μM).ALDH1A1-IN-3 is effective in improving glucose consumption in HepG2 cells.ALDH1A1-IN-3 can be used for studies to improve glucose metabolism.
价 格：￥电议型 号：T64228产 地：中国大陆
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T63341ALDH1A1-IN-2；ALDH1A1抑制剂2ALDH1A1-IN-2
ALDH1A1-IN-2 is a potent aldehyde dehydrogenase 1a1 (aldh1a1) inhibitor with anticancer activity.ALDH1A1-IN-2 may be used in the study of breast cancer, inflammation or obesity.
价 格：￥电议型 号：T63341产 地：中国大陆
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T62856FFA1 agonist-1；化合物 FFA1 agonist-1FFA1 agonist-1
FFA1 agonist-1 (Compound 17a) is an orally active fatty acid receptor (FFA1) agonist (EC50: 0.75 μM).
价 格：￥电议型 号：T62856产 地：中国大陆
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T62765WRNA10；化合物 WRNA10WRNA10
WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).
价 格：￥电议型 号：T62765产 地：中国大陆
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T62348A1AR antagonist 3；化合物 A1AR antagonist 3A1AR antagonist 3
A1AR antagonist 3 (compound 13) is a selective adenylate 1 (A1) receptor antagonist that acts on human A1 (Ki: 9.69 nM) and rat A1 (Ki: 0.529 nM). A1AR antagonist 3 can be used to study neurological diseases.
价 格：￥电议型 号：T62348产 地：中国大陆
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T62307Aha1/Hsp90-IN-1；化合物 Aha1/Hsp90-IN-1Aha1/Hsp90-IN-1
Aha1/Hsp90-IN-1 (Compound 17) is an inhibitor of the Aha1/Hsp90 complex and has an inhibitory effect on tau protein aggregation.Aha1/Hsp90-IN-1 disrupts the Aha1/Hsp90 interaction (IC50: 3.32 μM).
价 格：￥电议型 号：T62307产 地：中国大陆
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T62176POLA1 inhibitor 1；化合物 POLA1 inhibitor 1POLA1 inhibitor 1
POLA1 inhibitor 1 (Compound 12) is an orally active inhibitor of POLA1. POLA1 inhibitor 1 exhibits antitumour effects on several tumour tissue types and Adaroten-resistant cell lines.
价 格：￥电议型 号：T62176产 地：中国大陆
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T6217LFM-A13；化合物LFM-A13LFM-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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T62134A1/A3 AR antagonist 1；化合物 A1/A3 AR antagonist 1A1/A3 AR antagonist 1
A1/A3 AR antagonist 1 (Compound 10) is a potent, dual adenosine 1 (A1) and adenosine 3 (A3) receptor antagonist that acts on human A1 (Ki: 37.6 nM), human A3 (Ki: 25.4 nM) and rat A1 (Ki: 1.47 nM). 1 Can be used to study renal failure, inflammatory lung disease and Alzheimer´s disease.
价 格：￥电议型 号：T62134产 地：中国大陆
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T61744A1/A3 AR antagonist 2；化合物 A1/A3 AR antagonist 2A1/A3 AR antagonist 2
The compound is an a1/a3 adenosine receptor antagonist, which helps to treat (neurological) inflammatory diseases.
价 格：￥电议型 号：T61744产 地：中国大陆
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T61536A1AR antagonist 4；化合物 A1AR antagonist 4A1AR antagonist 4
A1AR antagonist 4 (compound 22) is a highly developed chemical compound that acts as a potent and selective antagonist of the A1 adenosine receptor (A1AR). It possesses a pIC50 value of 5.51 and a pKi value of 6.29 [1].
价 格：￥电议型 号：T61536产 地：中国大陆
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T61448AZA1；化合物AZA1Rac1/Cdc42-IN-1；Rac1/Cdc42-IN-1
AZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induced apoptosis of prostate cancer cells and inhibited cell proliferation, migration and invasion.
价 格：￥电议型 号：T61448产 地：中国大陆
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T61287CYP121A1-IN-1；化合物 CYP121A1-IN-1CYP121A1-IN-1
CYP121A1-IN-1 is a potent inhibitor of CYP121A1, demonstrating favorable activity against Mycobacterium tuberculosis (H37Rv MIC 90 ~6.25 μM, ~2.2 μg/mL). It significantly reduces mycocyclosin production by blocking the CYP121A1-mediated conversion of cyclo(l-tyrosyl-l-tyrosyl) to mycocyclosin [1].
价 格：￥电议型 号：T61287产 地：中国大陆
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T60915A1AR antagonist 5；化合物 A1AR antagonist 5A1AR antagonist 5
A1AR antagonist 5 (compound 20) is a potent and selective antagonist of A1 adenosine receptor (A1AR) with a pKi of 6.11 and a pIC 50 of 5.83 [1].
价 格：￥电议型 号：T60915产 地：中国大陆
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T60732A2A/A1 AR antagonist-1；化合物 A2A/A1?AR antagonist-1A2A/A1 AR antagonist-1
A2A/A1 AR antagonist-1 (compound 1a) has the potential for ischemic stroke research which is potent A 2A /A 1 AR dual antagonist with Ki s of 5.58 and 24.2 nM, respectively [1].
价 格：￥电议型 号：T60732产 地：中国大陆
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T60687A1AR antagonist 1；化合物 A1AR?antagonist 1A1AR antagonist 1
A1AR antagonist 1 (compound 18g) is a potent antagonist of A1 adenosine receptor (AR). A1AR antagonist 1 has Ki values of 2.08, 6.91, and 31.2 nM for hA1, hA2A and hA2B, respectively [1].
价 格：￥电议型 号：T60687产 地：中国大陆
