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T25549JCP174JCP174
JCP174 is a depalmitoylase inhibitor that enhances Toxoplasma host-cell invasion by targeting TgPPT1.
价 格：￥电议型 号：T25549产 地：中国大陆
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T8719SC99orally,ERK,c-Src,SC 99,ATP-binding,phosphorylation,platelet,AKT,Janus kinase,activation,anti-mye
SC99 is a selective inhibitor of JAK2-STAT3 activation. SC99 downregulates the expression of STAT3-modulated genes.SC99 inhibits platelet activation, aggregation and displays potent anti-myeloma, anti-thrombotic activities
价 格：￥电议型 号：T8719产 地：中国大陆
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T27703JZP-361
JZP-361 is a specific MAGL inhibitor with IC50s of 46 nM, 7.24 μM, and 1.79 μM for human recombinant MAGL, human recombinant FAAH, and human hABHD6. JZP-361 displays anti-histaminergic activities. JZP-361 can be used in studies about asthma.
价 格：￥电议型 号：T27703产 地：中国大陆
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TJS2216Aurantiamide acetateAurantiamide acetate,Inhibitor,cathepsin L,Piper aurantiacum,adjuvant-arthritic,
Aurantiamide acetate was isolated from the fermentation broth of Aspergillus penicilloides for the first time. Aurantiamide acetate is a selective and orally active cathepsin inhibitor. Aurantiamide acetate has anti-inflammatory activities and can be used for the study of inflammatory diseases[1][2].
价 格：￥电议型 号：TJS2216产 地：中国大陆
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TJS1779Protosappanin AProtosappanin A,inhibit,JAK,Inhibitor,STAT,Janus kinase
Protosappanin A has anti-oxidative/nitrative activities on brain immune and neuroinflammation through regulation of CD14/TLR4-dependent IKK/I??B/NF-??B inflammation signal pathway; it exerts anti-neuroinflammatory effect by inhibiting JAK2-STAT3 pathway in lipopolysaccharide-induced BV2 microglia. Protosappanin A induces immunosuppression of rats heart transplantation targeting T cells in grafts via NF-kappaB pathway. Protosappanin A and protosappanin B have antimicrobial activity, they show bot
价 格：￥电议型 号：TJS1779产 地：中国大陆
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T7677JNK Inhibitor VIIIJNK,inhibit,Inhibitor,JNK Inhibitor VIII
JNK Inhibitor VIII is an ATP-competitive selective inhibitor of c-Jun N-terminal kinase (JNK)(IC50 values of 45 nM and 160 nM for JNK-1 and -2, respectively).
价 格：￥电议型 号：T7677产 地：中国大陆
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T7767FMoc-Val-Cit-PAB-PNPFMocValCitPABPNP,ADC Linkers,inhibit,Antibody-drug conjugates linkers,Inhibitor,
Fmoc-Val-Cit-PAB-PNP is a linker for Antibody-Drug-Conjugation (ADC).
价 格：￥电议型 号：T7767产 地：中国大陆
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T6593ML324ML-324,Jumonji,periodontal,Cytomegalovirus,ML324,inhibit,simplex,CMV,Inhibitor,Herpes simplex v
ML324(IC50=920 nM) is a specific inhibitor of jumonji histone demethylase (JMJD2).
价 格：￥电议型 号：T6593产 地：中国大陆
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T9389Thalidomide-PEG4-PropargylE3 Ligase Ligand-Linker Conjugates,Thalidomide-PEG-4-Propargyl,inhibit,Inh
Thalidomide-PEG4-Propargyl is a synthetic E3 ligase ligand-linker conjugate containing a Thalidomide-based cereblon ligand and a linker which can be used in PROTAC technology[1].
价 格：￥电议型 号：T9389产 地：中国大陆
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TN71153,5-Dimethoxystilbeneinhibit,benzene extract,jack pine,3,5Dimethoxystilbene,3,5 Dimethoxystilbene,Pi
3,5-Dimethoxystilbene is a natural product isolated from the bark of jack pine (Pinus bunksiuna).
价 格：￥电议型 号：TN7115产 地：中国大陆
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T8313HCH6-1inhibit,inflammatory,FPR1,HCH6-1,cell infiltration,HCH6 1,antagonist,pulmonary,acute lung inju
HCH6-1 is a competitive Formyl peptide receptor 1 (FPR1) antagonist.
价 格：￥电议型 号：T8313产 地：中国大陆
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T9117BSJ-4-116CDK,degrader,antiproliferative,inhibit,Kelly,C1039F,BSJ 4 116,Cyclin dependent kinase,PROTA
BSJ-4-116 is a highly potent and selective CDK12 degrader (PROTAC) with an IC50 of 6 nM. It downregulates DDR genes through a premature termination of transcription, primarily through increasing poly(adenylation).
价 格：￥电议型 号：T9117产 地：中国大陆
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T9104TJ191cancer,TJ 191,Apoptosis,PMBC,MOLT-3,CEM,inhibit,C8166,Inhibitor,MOLT-4,MT-2,TJ191,HSB-2,TJ-191,
TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.
价 格：￥电议型 号：T9104产 地：中国大陆
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TJP2891MaltopentaoseEndogenous Metabolite,Maltopentaose,Inhibitor,inhibit
Maltopentaose is a maltooligosaccharide that is used for research and diagnostic purposes. They can also be used in nutrients and healthcare.
价 格：￥电议型 号：TJP2891产 地：中国大陆
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TQ0095BrincidofovirCMX 001,DNA,lipid-conjugated,Brincidofovir,CMX-001,HSV,Herpes simplex virus,Cytomegalov
Brincidofovir is an orally active, lipophilic form of cidofovir. It has enhanced activity compared to CDV against certain adenoviruses, herpesviruses, and orthopoxviruses.
价 格：￥电议型 号：TQ0095产 地：中国大陆
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T9236WSB1 Degrader 1E3 ligating enzyme,oral,inhibit,anticancer,Ubiquitin conjugating enzyme,Ubiquitin act
WSB1 Degrader 1 is a poten and orally active WD repeat and SOCS box-containing 1 degrader. WSB1 Degrader 1 has anticancer metastatic effects
价 格：￥电议型 号：T9236产 地：中国大陆
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T9073SRS16-86IRI,SRS16-86,Inhibitor,ferrostatin,SRS-16-86,ischemia-reperfusion injury,SCI,spinal cord inj
SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of?ferroptosis.
价 格：￥电议型 号：T9073产 地：中国大陆
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T9203JH-X-119-01inhibit,MYD88,IRAK,IL-1R associated kinase,Waldenstr?m,Inhibitor,IRAK1,Interleukin-1 rece
JH-X-119-01 is a highly potent and selective covalent inhibitor of IRAK-1.
价 格：￥电议型 号：T9203产 地：中国大陆
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T6S2115Ginkgolide Jinhibit,Ginkgolide J,Inhibitor
Ginkgolide J has neuroprotective activity, it can prevent A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices.
价 格：￥电议型 号：T6S2115产 地：中国大陆
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TP1906L1DPC AJ1951 acetateDPC AJ1951 acetate
DPC-AJ1951 acetate, a 14 amino acid peptide that acts as a potent agonist of the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR). And characterized the activity of DPC-AJ1951 acetate in ex vivo and in vivo assays of bone resorption[1].
价 格：￥电议型 号：TP1906L1产 地：中国大陆
