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TN1406DihydrokaempferolApoptosis,Dihydrokaempferol,Inhibitor,Bcl-2 Family,inhibit
Aromadendrin is a natural product. It induces apoptosis and inhibits Bcl-2 and Bcl-xL expression, possesses anti-inflammatory, antioxidant, and anti-diabetic properties, it exhibits anti-inflammatory activity
价 格：￥电议型 号：TN1406产 地：中国大陆
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T6121TepotinibMSC2156119；EMD-1214063；特泊替尼
Tepotinib is an inhibitor of MET tyrosine kinase with potential antineoplastic activity.
价 格：￥电议型 号：T6121产 地：中国大陆
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T5748IpecosideAIDS031406
AIDS031406 is a natural product Psychotria ipecacuanha.
价 格：￥电议型 号：T5748产 地：中国大陆
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T4554AG 1406
AG 1406 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2.
价 格：￥电议型 号：T4554产 地：中国大陆
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T16355NSC781406
NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).
价 格：￥电议型 号：T16355产 地：中国大陆
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T14069A-3 hydrochloride
A-3 hydrochloride is a potent, cell-permeable, reversible, ATP-competitive non-selective antagonist of various kinases. A-3 hydrochloride also inhibits PKC and casein kinase I with Ki values of 47 μM and 80 μM, respectively[1]. A-3 hydrochloride against P
价 格：￥电议型 号：T14069产 地：中国大陆
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T140659-Ethyladenine9-乙基腺嘌呤；6-Amino-9-ethylpurine
9-Ethyladenine is a partially effective inhibitor of APRT (adenine phosphoribosyltransferase)[1].
价 格：￥电议型 号：T14065产 地：中国大陆
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T140606-Maleimidocapronic acid
6-Maleimidocapronic acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T14060产 地：中国大陆
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T1406Amantadine hydrochloride1-Adamantylamine hydrochloride；Amantadine HCl；Symmetrel；1-Adamantanamine hyd
Amantadine hydrochloride is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease.
价 格：￥电议型 号：T1406产 地：中国大陆
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T1406Amantadine hydrochlorideAmantadine hydrochloride,1-Adamantylamine hydrochloride,CI-719
Amantadine hydrochloride is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease.
价 格：￥电议型 号：T1406产 地：美洲
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T140606-Maleimidocapronic acid6-Maleimidocapronic acid
6-Maleimidocapronic acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T14060产 地：美洲
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T140616-Maleimidohexanoic acid N-hydroxysuccinimide ester6-Maleimidohexanoic acid N-hydroxysuccinimide est
6-Maleimidohexanoic acid N-hydroxysuccinimide ester is a protective group in antibody drug conjugates.
价 格：￥电议型 号：T14061产 地：美洲
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T140637α,25-Dihydroxycholesterol7α,25-Dihydroxycholesterol,7α,25-OHC,
7α, 25-dihydroxycholesterol (7α,25-OHC) is a potent and selective agonist and endogenous ligand of the orphan GPCR receptor EBI2 (GPR183). 7α, 25-dihydroxycholesterol is highly potent at activating EBI2 (EC50=140 pM; Kd=450 pM). 7α, 25-dihydroxycholestero
价 格：￥电议型 号：T14063产 地：美洲
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T140648-Bromo-cGMP sodium8-Bromo-cGMP sodium
8-Bromo-cGMP sodium, a membrane-permeable analogue of cGMP, is a PKG (protein kinase G) activator. 8-Bromo-cGMP sodium has antinociceptive effects[2]. 8-Bromo-cGMP sodium significantly inhibits Ca2+ macroscopic currents and impairs insulin release stimula
价 格：￥电议型 号：T14064产 地：美洲
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T140659-Ethyladenine9-Ethyladenine
9-Ethyladenine is an APRT (adenine phosphoribosyltransferase) partially inhibitor of [1].
价 格：￥电议型 号：T14065产 地：美洲
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T140669-ING-419-ING-41
9-ING-41 is a potent glycogen synthase kinase-3 (GSK-3) inhibitor[1]. 9-ING-41 induces apoptosis and cell cycle arrest at prophase by targeting centrosomes and microtubule-bound GSK-3β. 9-ING-41 has anticancer activity[2].
价 格：￥电议型 号：T14066产 地：美洲
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T14067A-1165442A-1165442
A-1165442 is a competitive TRPV1 antagonist. For human TRPV, the IC50 values is 9 nM.
价 格：￥电议型 号：T14067产 地：美洲
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T16355NSC781406NSC781406
NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).
价 格：￥电议型 号：T16355产 地：美洲
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T4554AG 1406AG 1406
AG 1406 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2.
价 格：￥电议型 号：T4554产 地：美洲
