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产品数：86101
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T9859SW209049Compound 1673558592,Compound 1673558 59 2
SW209049 is a stearoyl-CoA 9-desaturase inhibitor. SW209049 exhivits potent activity against H2122 cell with IC50 of 0.13uM.
价 格：￥电议型 号：T9859产 地：中国大陆
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T100732-Iodomelatonin2Iodomelatonin,2 Iodomelatonin
2-Iodomelatonin is a potent agonist of melatonin receptor 1 (MT1) with a Ki value of 28 pM, it is more 5-fold selective for MT1 over MT2. 2-iodomelatonin can be used to identify, characterize and localize melatonin binding sites in the brain and peripheral tissues.
价 格：￥电议型 号：T10073产 地：中国大陆
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T7369GemigliptinInhibitor,DPP,Gemigliptin,Dipeptidyl Peptidase,inhibit
Gemigliptin is a potent dipeptidyl peptidase-4 (DPP-4) inhibitor(KD : 7.25 nM.)
价 格：￥电议型 号：T7369产 地：中国大陆
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T17325Pomalidomide-PEG4-C-COOHInhibitor,Pomalidomide PEG4 C COOH,PomalidomidePEG4CCOOH,inhibit,E3 Ligase L
Pomalidomide-PEG4-C-COOH is a synthesized E3 ligase ligand-linker conjugate that combines the Pomalidomide-based cereblon ligand and 4-unit PEG linker used in PROTAC technology.
价 格：￥电议型 号：T17325产 地：中国大陆
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T94734SC-203tumor,antineoplastic,Fms like tyrosine kinase 3,Vascular endothelial growth factor receptor,4
4SC-203 is a multikinase inhibitor with potential antineoplastic activity. 4SC-203 selectively inhibits FMS-related tyrosine kinase 3 (FLT3/STK1), FLT3 mutated forms, and vascular endothelial growth factor receptors (VEGFRs).
价 格：￥电议型 号：T9473产 地：中国大陆
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T6421BRD73954Inhibitor,BRD73954,Ac-Tubulin,inhibit,α-tubulin acetylation,HeLa cells,BRD-73954,BRD 73954,H
BRD73954, an effective and specific HDAC inhibitor, which is with IC50 of 36 nM and 120 nM for HDAC6 and HDAC8, respectively.
价 格：￥电议型 号：T6421产 地：中国大陆
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T8732CTPI-2macrophage,carrier,CTPI-2,NSCLC,transporter,glucose,steatohepatitis,CTPI 2,Mitochondrial Metab
CTPI-2 is an inhibitor of mitochondrial citrate carrier SLC25A1 with(KD : 3.5 μM). CTPI-2 inhibits glycolysis, PPARγ, and its downstream target the glucose transporter GLUT4. CTPI-2 exhibits anti-tumor activity.CTPI-2 halts salient alterations of NASH reverting steatosis, preventing the evolution to steatohepatitis, reducing inflammatory macrophage infiltration in the liver and adipose tissue, and starkly mitigating obesity induced by a high-fat diet.
价 格：￥电议型 号：T8732产 地：中国大陆
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T9357Ro 5212773Ro-5212773,Inhibitor,Ro 5212773,neuronal,inhibit,Ro5212773,mesolimbic,system,TAAR1,GPCR
EPPTB is a selective TAAR1 antagonist.
价 格：￥电议型 号：T9357产 地：中国大陆
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T8734Cholineapoptosis,orally active,inhibit,hydrogen oxidized,organic base,sphingomyelin,Choline,standard
Choline is a ubiquitous water soluble nutrient, often associated with the B vitamins
价 格：￥电议型 号：T8734产 地：中国大陆
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T6731WYE-354inhibit,Apoptosis,WYE354,WYE-354,WYE 354,Inhibitor,Autophagy,Mammalian target of Rapamycin,mT
WYE-354(IC50=5 nM) is an effective, selective and ATP-competitive mTOR inhibitor. It blocks mTORC2/P-AKT(S473) and mTORC1/P-S6K(T389), not P-AKT(T308). The selectivity for mTOR is higher than PI3Kα (>100-fold) and PI3Kγ (>500-fold).
价 格：￥电议型 号：T6731产 地：中国大陆
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T7739L-Leucyl-L-Leucine methyl ester hydrochloridelymphocytes,leukocytes,monocytes,pathway,LLeucylLLeucin
Leu-Leu-ome hydrochloride is a lysosomal condensation product that cytotoxic towards natural killer cells and CD4+ and CD8+ T lymphocytes.
价 格：￥电议型 号：T7739产 地：中国大陆
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T7315BAY1125976inhibit,Inhibitor,Protein kinase B,Akt,BAY 1125976,BAY1125976,PKB,BAY-1125976
BAY1125976 is an allosteric inhibitor of Akt1 and Akt2 (IC50s of 5.2 and 18 nM, respectively, in a time-resolved FRET assay)
价 格：￥电议型 号：T7315产 地：中国大陆
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T7375A-836339A-836339,A 836339,Cannabinoid Receptor,A836339,inhibit,Inhibitor
A-836339 acts as a potent cannabinoid receptor full agonist which has a higher affinity for the peripheral CB2 receptor (Ki = 0.64 nM) over the central CB1 receptor (Ki = 270 nM). It displays analgesic, anti-inflammatory, and anti-hyperalgesic effects in mice.
价 格：￥电议型 号：T7375产 地：中国大陆
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T12849SAR7334SAR7334,SAR 7334,TRP Channel,SAR-7334,Inhibitor,inhibit,Transient receptor potential channels
SAR7334 is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
价 格：￥电议型 号：T12849产 地：中国大陆
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T7301BDP5290inhibit,Rho-kinase,Rho-associated kinase,BDP-5290,BDP5290,Rho-associated protein kinase,ROK,B
BDP5290 is a potent inhibitor of both ROCK and MRCK(IC50s of 5 nM, 50 nM, 10 nM and 100 nM for ROCK1, ROCK2, MRCKα and MRCKβ, respectively.)
价 格：￥电议型 号：T7301产 地：中国大陆
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T7308NomifensineDopamine Receptor,Inhibitor,Nomifensine,inhibit
Nomifensine is a norepinephrine-dopamine reuptake inhibitor that prevents dopamine reuptake into synaptosomes.
价 格：￥电议型 号：T7308产 地：中国大陆
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T60073WAY-658650WAY 658650,WAY658650
WAY-658650 has antibacterial activity against Mycobacterium tuberculosis.
价 格：￥电议型 号：T60073产 地：中国大陆
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T9173HM-30181 mesylate monohydrateHM30181 mesylate monohydrate,HM 30181 mesylate monohydrate
HM-30181 mesylate monohydrate is an oral P-glycoprotein (P-gp) inhibitor, used to enhance the oral bioavailability of P-gp substrate drugs.
价 格：￥电议型 号：T9173产 地：中国大陆
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TP1736LFibrinogen-Binding Peptide 137235-80-4(fb-acetate)Fibrinogen Binding Peptide 137235 80 4(fb acetate)
Fibrinogen-Binding Peptide (designed by anticomplementarity hypothesis) is a presumptive peptide mimic of the vitronectin binding site on the fibrinogen receptor. Fibrinogen-Binding Peptide binds fibrinogen and inhibits both the adhesion of platelets to fibrinogen and platelet aggregation, and also inhibits the adhesion of platelets to vitronectin
价 格：￥电议型 号：TP1736L产 地：中国大陆
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T6692TAK-733inhibit,Inhibitor,TAK-733,MAP2K,MAPKK,MEK,Mitogen-activated protein kinase kinase
MEK Inhibitor TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
价 格：￥电议型 号：T6692产 地：中国大陆
