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T11024DHODH-IN-15DHODH IN 15,DHODHIN15
DHODH-IN-15 is the hydroxyfuran analogue of A771726. DHODH-IN-15 is a dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 11 μM for rat liver DHODH. DHODH-IN-15 can be used for rheumatoid arthritis.
价 格：￥电议型 号：T11024产 地：中国大陆
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T11029hDHODH-IN-5
hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH, IC50 = 0.91 μM).
价 格：￥电议型 号：T11029产 地：中国大陆
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T19783DehydroabiethylaminePyruvate dehydrogenase kinase,PDH kinase,Dehydroabiethylamine,Inhibitor,PDHK,Can
Dehydroabiethylamine is an inducer of hepatic CYP2B activity. Dehydroabiethylamine inhibits pyruvate dehydrogenase kinases (PDKs) and intracellular cholesterol transport with anti-tumor activity.
价 格：￥电议型 号：T19783产 地：中国大陆
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T8820BML-284 hydrochlorideBML284 hydrochloride,AGS,TCF,N-cadherin,Wnt,BML284,cardiac defect,MNK45,BML 284
BML-284 HCL is a potent, selective Wnt canonical signaling activator and tubulin polymerization inhibitor.
价 格：￥电议型 号：T8820产 地：中国大陆
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T7776ADH-503tumor-infiltrating,CD11b,ADH-503,Inhibitor,tumorassociated,dendritic,immunosuppressive,macrop
ADH-503 is a potent agonist of the integrin CD11b to mitigate myeloid cell immunosuppression.
价 格：￥电议型 号：T7776产 地：中国大陆
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T8536FilastatinC. albicans,Fungal,promoter,Antifungal,adhesion,filamentation,inhibit,polystyrene,Inhibito
Filastatin is a long-lasting inhibitor of Candida albicans filamentation, and has potent antifungal effect.
价 格：￥电议型 号：T8536产 地：中国大陆
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T11030DHODH-IN-8DHODHIN8,DHODH IN 8
DHODH-IN-8 has antimalarial activity. DHODH-IN-8 is an inhibitor of human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) with IC50 of 0.13 μM and 47.4 μM, and Kis of 0.016 μM and 5.6 μM, respectively.
价 格：￥电议型 号：T11030产 地：中国大陆
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T7338DHBP dibromideCa channels,inhibit,DHBP dibromide,Inhibitor,Ca2+ channels,Calcium Channel
DHBP dibromide is calcium release and a muscle relaxant inhibitor.
价 格：￥电议型 号：T7338产 地：中国大陆
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T7307Vorasidenibinhibit,AG 881,Vorasidenib,AG881,Inhibitor,Isocitrate Dehydrogenase (IDH)
Vorasidenib is an inhibitor of mutant isocitrate dehydrogenase (IDH; IC50s = 31.9 and 31.7 nM for IDH1R132H and IDH2R140Q, respectively)
价 格：￥电议型 号：T7307产 地：中国大陆
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T6964ResiquimodHepatitis C virus,R-848,S-28463,R 848,S 28463,Toll-like Receptor (TLR),Inhibitor,Resiquimo
Resiquimod is an imidazoquinoline amine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through the TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages, and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activation of other transcription factors. This may lead to an increase in mRNA levels and subsequent production of cytokin
价 格：￥电议型 号：T6964产 地：中国大陆
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T6697TCIDhydrolase,C-terminal,Neuronal,Deubiquitinase,transporter,ubiquitination,DUBs,inhibit,TCID,glycin
TCID(IC50=0.6 μM) is a DUB inhibitor of ubiquitin C-terminal hydrolase L3. It has the 125-fold selectivity to L1.
价 格：￥电议型 号：T6697产 地：中国大陆
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T7064Valproic AcidHistone deacetylases,Mitochondrial Autophagy,bipolar disorder,epilepsy,Autophagy,Apopto
Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally,
价 格：￥电议型 号：T7064产 地：中国大陆
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T11027DHODH-IN-4DHODHIN4,DHODH IN 4
DHODH-IN-4 is a human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) inhibitor. The IC50 values of PfDHODH and HsDHODH are 4 μM and 0.18 μM, respectively. DHODH-IN-4 has antimalarial activity.
价 格：￥电议型 号：T11027产 地：中国大陆
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T7119Y15PTK2 protein tyrosine kinase 2,FAK Inhibitor-14,FAK Inhibitor14,Y15,Y 15,FAK,PTK2,Focal adhesion
Y15 is a potent and specificsmall-molecule FAK scaffolding inhibitor that inhibits its autophosphorylation activity, blocks tumor growth.
价 格：￥电议型 号：T7119产 地：中国大陆
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T6903NCT-501Inhibitor,Aldehyde Dehydrogenase (ALDH),inhibit,NCT-501,NCT 501
NCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.
价 格：￥电议型 号：T6903产 地：中国大陆
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T7488BD1063 dhydrochlorideSigma Receptor,Inhibitor,inhibit,BD1063 dhydrochloride,BD-1063 dhydrochloride
BD1063 is a potent and selective sigma 1(σ1) receptor antagonist(Ki = 9 nM).
价 格：￥电议型 号：T7488产 地：中国大陆
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TN1433Batatasin IIIFocal adhesion kinase,Batatasin III,Inhibitor,inhibit,PTK2 protein tyrosine kinase 2,PK
Batatasin III inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition and FAK-AKT signals and possesses anti-cancer activities. Batatasin III has a long-term inhibitory effect on whole-plant growth and shows germination
价 格：￥电议型 号：TN1433产 地：中国大陆
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T11019DHODH-IN-1DHODHIN1,DHODH IN 1
DHODH-IN-1 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 25 nM. DHODH-IN-1 is an inhibitor of the pyrimidine biosynthetic pathway.
价 格：￥电议型 号：T11019产 地：中国大陆
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T11031hDHODH-IN-7hDHODH IN 7,hDHODHIN7
hDHODH-IN-7 is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor. hDHODH-IN-7 and pMIC50 of 7.4 have antiviral effects.
价 格：￥电议型 号：T11031产 地：中国大陆
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TP1939L1RVD-Hpα acetate(1193362-76-3 free base)RVD Hpα acetate(1193362 76 3 free base),RVDHpα acetate(119336
RVD-Hpα acetate is the N-terminally extended form of human hemopressin that acts as a selective CB1 receptor agonist. Increases intracellular Ca2+ levels in cells expressing CB1 receptors in vitro. Also high affinity CB2 positive allosteric modulator (Ki = 50 nM).
价 格：￥电议型 号：TP1939L1产 地：中国大陆
