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T9703LGSK778 hydrochlorideGSK778 hydrochloride
GSK778 hydrochloride hydrochloride is a potent and selective BD1 bromodomain inhibitor of the BET proteins, with IC50s of 75 nM (BRD2 BD1), 41 nM (BRD3 BD1), 41 nM (BRD4 BD1), and 143 nM (BRDT BD1), respectively. GSK778 hydrochloride hydrochloride phenocopies the effects of pan-BET inhibitors in cancer models[1].
价 格：￥电议型 号：T9703L产 地：中国大陆
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T20797NE-100 hydrochloride?NE100 hydrochloride?,NE100,inhibit,Inhibitor,NE 100 hydrochloride?,Sigma Recept
NE100 HCl is a potent and selective antagonist of σ1 (IC50 = 4.16 nM) with antipsychotic activity. NE100 HCl also suppresses ER stress-induced hippocampal cell death.
价 格：￥电议型 号：T20797产 地：中国大陆
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T37097SET 2SET 2
SET 2 is an antagonist of transient receptor potential vanilloid type 2(TRPV2) with an IC50 of 0.46 μM. SET 2 shows selectivity over TRPV1, TRPV3 and TRPV4.
价 格：￥电议型 号：T37097产 地：中国大陆
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T9787suvn-911nicotinic,antidepressant,nAChR,acetylcholine,neuronal,Inhibitor,SUVN-911,suvn911,suvn 911,de
suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity.
价 格：￥电议型 号：T9787产 地：中国大陆
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TP1997L[Ala17]-MCH acetate
[Ala17]-MCH acetate is a selective ligand for MCHR1 with a Ki of 0.16 nM and Kd of 0.37 nM(Eu3+ chelate-labeled). [Ala17]-MCH acetate shows selectivity over MCHR2 with Ki of 34 nM.
价 格：￥电议型 号：TP1997L产 地：中国大陆
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T8497SX-682cells,SX-682,allosteric,SX 682,recruitment,suppressor,Inhibitor,tumor,CXCR,CXC chemokine recep
SX-682 is a potent, selective and orally bioavailable inhibitor of CXCR1/2 ,has the potential to treat castration-resistant prostate cancer.
价 格：￥电议型 号：T8497产 地：中国大陆
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T6970RK33RK33
RK-33 is a first-in-class small molecule inhibitor of DDX3 (a RNA helicase) and causes G1 cell cycle arrest, induces apoptosis, and promotes radiation sensitization in DDX3-overexpressing cells.
价 格：￥电议型 号：T6970产 地：中国大陆
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T9756AZD-9574PPAR,Peroxisome proliferator-activated receptors,breast cancer,inhibit,AZD-9574,HRR,HRR-defi
AZD-9574 is a selective inhibitor of PARP1 at the sites of SSBs. AZD-9574 exhibits anti-cancer activities and can be used in studies about HRD+ breast cancer and advanced solid malignancies.
价 格：￥电议型 号：T9756产 地：中国大陆
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T6496Vactosertibantimetastatic,invasion,Smad,TEW7197,Transforming growth factor beta receptors,TGFβ,migra
Vactosertib is an orally bioavailable inhibitor of the serine/threonine kinase, transforming growth factor (TGF)-beta receptor type 1 (TGFBR1), also known as activin receptor-like kinase 5 (ALK5), with potential antineoplastic activity.
价 格：￥电议型 号：T6496产 地：中国大陆
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T9825CORT-108297 EnantiomerCORT108297 Enantiomer,CORT 108297 Enantiomer
CORT-108297 Enantiomer is an enantiomer of CORT-108297 which is an antagonist of the Glucocorticoid Receptor.
价 格：￥电议型 号：T9825产 地：中国大陆
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T9978Glutathione synthesis-IN-1Glutathione synthesisIN1,Glutathione synthesis IN 1
Glutathione synthesis-IN-1 (DC-1) is a inhibitor of glutathione synthesis[1].
价 格：￥电议型 号：T9978产 地：中国大陆
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T9843WAY-297342WAY 297342,WAY297342
FLT3-IN-16 exhibits potent inhibitory activity against FLT3 tyrosine kinase with an IC 50 of 1.1 μM. FLT3-IN-16 can be used for researching acute myeloid leukemia [1].
价 格：￥电议型 号：T9843产 地：中国大陆
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T8151MobocertinibAP-32788,Epidermal growth factor receptor,TAK-788,H1975,Inhibitor,Mobocertinib,HCC827,in
Mobocertinib is a potent inhibitor of epidermal growth factor receptor (EGFR) and an antineoplastic agent
价 格：￥电议型 号：T8151产 地：中国大陆
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T22812GRI977143GRI977143,GRI-977143
GRI977143 is a selective and non-lipid agonist of LPA2 (EC50 = 3.3 μM). GRI977143 inhibits the activation of caspases 3, 7, 8, and 9 and and reduces DNA fragmentation.
价 格：￥电议型 号：T22812产 地：中国大陆
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T9750Cetyldimethylethylammonium Bromideintracellular,ions,staining,removal,inhibit,Inhibitor,Cetyldimethy
Cetyldimethylethylammonium Bromide can be used to induce extracellular secretion of beta-galactosidase.
价 格：￥电议型 号：T9750产 地：中国大陆
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T8943AKOS025692697AKOS-025692697,AKOS025692697
AKOS025692697 is a biochemical.
价 格：￥电议型 号：T8943产 地：中国大陆
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T60063WAY-323975
WAY-323975 is a nonfluorescent inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pairn.
价 格：￥电议型 号：T60063产 地：中国大陆
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T39705ATG7-IN-1ATG7 IN 1,ATG7IN1,ATG-7-IN-1
ATG7-IN-1 is a selective ATG7 inhibitor with an IC50 of 62 nM.
价 格：￥电议型 号：T39705产 地：中国大陆
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T9734Benzo[b]thiophene-2-sulfonamide, N-[3-(aminomethyl)phenyl]-5-chloro-3-methyl-Benzo[b]thiophene2sulfo
Benzo[b]thiophene-2-sulfonamide, N-[3-(aminomethyl)phenyl]-5-chloro-3-methyl- directly inhibits InhA and does not require activation by the catalase peroxidase KatG.
价 格：￥电议型 号：T9734产 地：中国大陆
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T8974ML-211MAGL,ML 211,inhibit,Phospholipase,Monoacylglycerol lipase,ML-211,Inhibitor,ML211
ML-211 is a carbamate-based dual inhibitor of LYPLA1 (IC50 = 17 nM) and the related LYPLA2 (IC50 = 30 nM)
价 格：￥电议型 号：T8974产 地：中国大陆
