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T0261AmcinonideAmcinonide,CL-34699,
Amcinonide is a Corticosteroid. The mechanism of action of amcinonide is as a Corticosteroid Hormone Receptor Agonist.
价 格：￥电议型 号：T0261产 地：美洲
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T0346CamylofinCamylofin,Camylofine,Acamylophenine
Camylofin is an antimuscarinic, used for relaxing smooth muscle.
价 格：￥电议型 号：T0346产 地：美洲
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T13461-Phenyl-1,2-ethanediol1-Phenyl-1,2-ethanediol
1-Phenyl-1,2-ethanediol is O-benzyl oxime ether derivatives and used as pesticides.
价 格：￥电议型 号：T1346产 地：美洲
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T13461(+)-Cloprostenol(+)-Cloprostenol,D-Cloprostenol,
(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.
价 格：￥电议型 号：T13461产 地：美洲
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T13462(+)-DHMEQ(+)-DHMEQ,(1R,2R,6R)-Dehydroxymethylepoxyquinomicin,(1R,2R,6R)-DHMEQ
(+)-DHMEQ is an antioxidant transcription factor Nrf2 activator. (+)-DHMEQ is the enantiomer of (-)-DHMEQ.
价 格：￥电议型 号：T13462产 地：美洲
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T13463L2Dihydrexidine hydrochlorideDihydrexidine hydrochloride,DAR-0100 hydrochloride,
Dihydrexidine hydrochloride is a full efficacy D1-like dopamine receptor (D1/D5) agonist (IC50: 10 nM for D1 receptor). Dihydrexidine hydrochloride also shows potent antiparkinsonian activity.
价 格：￥电议型 号：T13463L2产 地：美洲
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T13464(+)-Ketoconazole(+)-Ketoconazole,(+)-Ketoconazol,(+)-R 41400
(+)-Ketoconazole is an agent of imidazole anti-fungal, and is an inhibitor of CYP3A4.
价 格：￥电议型 号：T13464产 地：美洲
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T13465(+)-Penbutolol(+)-Penbutolol,(R)-Penbutolol,(+)-Isopenbutolol
(+)-Penbutolol is an antagonist of β-adrenoceptor(IC50 of 0.74 μM). (+)-Penbutolol is an optical isomer of l-penbutolol with Na+ channel-blocking action.
价 格：￥电议型 号：T13465产 地：美洲
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T13466(+)-Talarozole(+)-Talarozole
(+)-Talarozole is a potent retinoic acid metabolism inhibitor .
价 格：￥电议型 号：T13466产 地：美洲
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T13467(±)-BAY-1251152(±)-BAY-1251152
(±)-BAY-1251152 is a racemic mixture of BAY-1251152. BAY-1251152 is highly selective inhibitor of PTEF/CDK9.
价 格：￥电议型 号：T13467产 地：美洲
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T13469(±)-Huperzine A(±)-Huperzine A
(±)-Huperzine A, an active Lycopodium alkaloid, and is a selective and reversible inhibitor of acetylcholinesterase (AChE) and has been used treatment of Alzheimer´s disease (AD).
价 格：￥电议型 号：T13469产 地：美洲
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T15199EdicotinibEdicotinib,JNJ-40346527,JNJ-527
Edicotinib shows less inhibitory effects on KIT and FLT3 (IC50: 20 nM and 190 nM, respectively). Edicotinib is a brain penetrant and orally active inhibitor of colony-stimulating factor-1 receptor (IC50: 3.2 nM). Edicotinib limits microglial expansion an
价 格：￥电议型 号：T15199产 地：美洲
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T16346NS1652NS1652
NS1652 is a reversible anion conductance inhibitor. NS1652 blocks chloride channel has an IC50 of 1.6 μM in human and mouse red blood cells.
价 格：￥电议型 号：T16346产 地：美洲
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T16791RottlerinRottlerin,Mallotoxin,NSC 56346
Rottlerin is a natural product purified from Mallotus Philippinensis and is a specific PKC inhibitor (IC50: PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM). Rottlerin causes apoptosis via caspase 3 activation.
价 格：￥电议型 号：T16791产 地：美洲
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T1867ATB 346ATB 346
ATB-346 is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.
价 格：￥电议型 号：T1867产 地：美洲
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T2024A-803467A-803467,A803467,A 803467
A-803467 is a selective NaV1.8 channel blocker.
价 格：￥电议型 号：T2024产 地：美洲
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T2346EnasidenibEnasidenib,AG-221,
Enasidenib is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
价 格：￥电议型 号：T2346产 地：美洲
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T8346910m/ZS44；化合物 10m/ZS4410m/ZS44
10m/ZS44, a blood-brain barrier-permeable Glioblastoma (GBM) inhibitor, significantly suppresses tumor growth in mouse xenograft models and induces apoptosis through activation of the SIRT1/p53-mediated pathway, thereby reducing U251 cell proliferation [1].
价 格：￥电议型 号：T83469产 地：中国大陆
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T8346810NH2-11F-Camptothecin；化合物 10NH2-11F-Camptothecin10NH2-11F-Camptothecin
10NH2-11F-Camptothecin, an antibody-drug conjugate (ADC), exhibits antitumor activity and is utilized in cancer research [1].
价 格：￥电议型 号：T83468产 地：中国大陆
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T8346710-O-Trans-p-methoxycinnamoylcatalpol；化合物 10-O-Trans-p-methoxycinnamoylcatalpol10-O-Trans-p-methoxyc
10-O-Trans-p-methoxycinnamoylcatalpol exhibits antioxidant properties, demonstrated by an IC50 of 0.37 μM/mL in the DPPH free radical scavenging assay [1] [2].
价 格：￥电议型 号：T83467产 地：中国大陆
