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T62360AChE-IN-26
AChE-IN-26 is an AChE (acetylcholinesterase) inhibitor (IC50= 0.42 μM). AChE-IN-26 has research value in Alzheimer’s disease.
价 格：￥电议型 号：T62360产 地：中国大陆
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T60082HDAC-IN-40HDACIN40,HDAC IN 40
HDAC-IN-40 is a potent alkoxyamide-based HDAC inhibitor with Ki of 60 nM and 30 nM for HDAC2 and HDAC6, respectively. HDAC-IN-40 had antitumor effects
价 格：￥电议型 号：T60082产 地：中国大陆
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T60148MSC-4106MSC4106
MSC-4106 is an orally active and potent inhibitor of YAP/TAZ-TEAD. MSC-4106 inhibits TEAD1 or TEAD3 auto-palmitoylation and exhibits inhibitory effect on NCI-H226 tumor xenograft model [1].
价 格：￥电议型 号：T60148产 地：中国大陆
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T60187RP-6685RP6685
RP-6685 is a potent, selective and orally active DNA polymerase theta (Polθ) inhibitor with an IC 50 value of 5.8 nM in PicoGreen assay. RP-6685 shows antitumor efficacy in mouse tumor xenograft model [1].
价 格：￥电议型 号：T60187产 地：中国大陆
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TQ0009UCB9608Phosphatidylinositol 4 kinases,UCB-9608,Inhibitor,UCB 9608,UCB9608,PI4 kinases,PI4K,inhibit
UCB9608 is a selective and orally active PI4KIIIβ inhibitor (IC50: 11 nM), selective over PI3KC2 α, β, and γ lipid kinases.
价 格：￥电议型 号：TQ0009产 地：中国大陆
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T9235GW604714XInhibitor,mitochondrial respiration,Mitochondrial Metabolism,Parkinson’s Disease,MCT1,GW604
GW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate
价 格：￥电议型 号：T9235产 地：中国大陆
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T602484-Aminobenzamidine dihydrochloride
4-Aminobenzamidine (p-Aminobenzamidine) dihydrochloride is a strong trypsin inhibitor and a relatively weak inhibitor of urokinase type plasminogen activator (uPA) (K i =82 μM). 4-Aminobenzamidine can inhibit growth of a human prostate tumor in SCID mice [1] [2].
价 格：￥电议型 号：T60248产 地：中国大陆
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T60278Tyrosinase-IN-2
Tyrosinase-IN-2 (compound 67) is a potent tyrosinase inhibitor. Tyrosinase is a copper-containing metalloenzyme that is responsible for the rate-limiting catalytic step in the melanin biosynthesis and enzymatic browning. Tyrosinase-IN-2 has the potential for the research of skin whitening agents and food preservatives [1].
价 格：￥电议型 号：T60278产 地：中国大陆
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TN1601EffusolInhibitor,Effusol,inhibit
Effusol is a natural product, exhibits potent scavenging activity for DPPH and ABTS radicals(IC50 values of 79 μM and 2.73 μM, respectively). Effusol rescues CA1 LTP attenuated by corticosterone, defending the hippocampal function against stress-induced cognitive decline. Effusol can induce caspase-3-mediated cytotoxicity in HT22 cells.
价 格：￥电议型 号：TN1601产 地：中国大陆
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T7600FucoxanthinFucoxanthin,Inhibitor,inhibit
Fucoxanthin is a carotenoid that occurs naturally in certain algae. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color.It shows anti-obesity, anti-oxidant, anti-diabetic, anticancer and anti-inflammatory activities.
价 格：￥电议型 号：T7600产 地：中国大陆
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T21060LNPC 567 acetateNPC 567 acetate
NPC 567 acetate is a bradykinin B2 antagonist and can be used in studies about the treatment of allergic airway disease.
价 格：￥电议型 号：T21060L产 地：中国大陆
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T60093CHEMBL1380345
CHEMBL1380345 exhibits antibacterial activity against Staphylococcus aureus, Bacillus cereus, and Escherichia coli with pMIC values of 3.64, 3.56, and 3.70, respectively.
价 格：￥电议型 号：T60093产 地：中国大陆
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T60108PDGFR Tyrosine Kinase Inhibitor III
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格：￥电议型 号：T60108产 地：中国大陆
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T60757SB-216
SB-216 is able to be used for the research of cancer which is a potent inhibitor of tubulin polymerization. SB-216 exhibits strong antiproliferative potency in a panel of human cancer cell lines, including melanoma, breast cancer, and lung cancer [1].
价 格：￥电议型 号：T60757产 地：中国大陆
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T7127DC260126stress,DC260126,DC-260126,FFAR,Inhibitor,insulin,inhibit,secretion,Apoptosis,DC 260126,Free
DC260126 is a small-molecule antagonist of FFA1 (GPR40)
价 格：￥电议型 号：T7127产 地：中国大陆
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T6557KU-0060648mTOR,inhibit,KU-0060648,Phosphoinositide 3-kinase,Inhibitor,Mammalian target of Rapamycin,
KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM.
价 格：￥电议型 号：T6557产 地：中国大陆
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T60081BV02
BV02 is an inhibitor of 14-3-3 protein-protein interactions and can be used in studies about the treatment of chronic myeloid leukemia. BV02 disrupts hematopoietic cells expressing the IM-resistant T315I mutation and the IM-sensitive wild-type Bcr-Abl.
价 格：￥电议型 号：T60081产 地：中国大陆
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T60156PBRM1-BD2-IN-2PBRM1BD2IN2
PBRM1-BD2-IN-2 is a selective and cell-active polybromo-1 (PBRM1) bromodomain inhibitor. PBRM1-BD2-IN-2 has binding affinity and inhibitory activity for PBRM1-BD2 with Kd and IC50 values of 9.3 μM and 1.0 μM, respectively. PBRM1-BD2-IN-2 can be used for the research of cancer.
价 格：￥电议型 号：T60156产 地：中国大陆
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T60145CCR6 antagonist 1CCR6antagonist1
CCR6 antagonist 1 is a CCR6 antagonist. CCR6 antagonist 1 inhibits the CCL20/CCR6 axis. CCR6 antagonist 1 can be used in the research of autoimmune-mediated inflammatory diseases, such as inflammatory bowel diseases (IBDs).
价 格：￥电议型 号：T60145产 地：中国大陆
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