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T71876F1386-0303;化合物 F1386-0303F1386-0303
F1386-0303 is a novel potent and selective MAP4K4 inhibitor.
价 格:¥电议型 号:T71876产 地:中国大陆
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T71389Fluoxetine oxalate;化合物 Fluoxetine oxalateFluoxetine oxalate
Fluoxetine oxalate is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used for the treatment of major depressive disorder, obsessive–compulsive disorder, bulimia nervosa, panic disorder, and premenstrual dysphoric disorder.
价 格:¥电议型 号:T71389产 地:中国大陆
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T71388Desaspidin;化合物 DesaspidinDesaspidin
Desaspidin is an anthelmintic. Desapidin may occur in natural form within some plants such as Coastal woodfern, Dryopteris arguta. Since the 1950s the inhibition effects of desapidins upon phosphorylation in chloroplasts has been noted and studied.
价 格:¥电议型 号:T71388产 地:中国大陆
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T71387Neratinib maleate monohydrate;化合物 Neratinib maleate monohydrateNeratinib maleate monohydrate
Neratinib maleate monohydrate is an irreversible inhibitor of the HER-2 receptor tyrosine kinase with potential antineoplastic activity.
价 格:¥电议型 号:T71387产 地:中国大陆
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T71386GW-597901 cinnamate;化合物 GW-597901 cinnamateGW-597901 cinnamate
GW-597901 cinnamate is a long-acting beta(2)-agonist.
价 格:¥电议型 号:T71386产 地:中国大陆
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T71385Aroplatin;化合物 AroplatinAroplatin
Aroplatin is a synthetic liposomal formulation of bis-neodecanoate diaminocyclohexane platinum (NDDP), a third-generation platinum complex analogue of cisplatin, with potential antineoplastic activity. After displacement of the 2 long-chain aliphatic leaving groups (neodecanoic acid), platinum diaminocyclohexane (DACH) complexes become highly reactive and alkylate macromolecules, forming both inter- and intra-strand DNA crosslinks and inhibiting DNA synthesis, which results in tumor cell cytotox
价 格:¥电议型 号:T71385产 地:中国大陆
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T71384Cenisertib benzoate;化合物 Cenisertib benzoateCenisertib benzoate
Cenisertib benzoate is an orally bioavailable, synthetic, small-molecule multi-Aurora kinase inhibitor with potential antineoplastic activity.
价 格:¥电议型 号:T71384产 地:中国大陆
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T71383NB-533;化合物 NB-533NB-533
NB-533 is a macrocyclic peptidic BACE-1 inhibitor.
价 格:¥电议型 号:T71383产 地:中国大陆
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T71382KRC-108;化合物 KRC-108KRC-108
KRC-108 is a multiple kinase inhibitor. KRC-108 is a potent inhibitor of Ron, Flt3 and TrkA as well as c-Met. KRC-108 inhibited oncogenic c-Met M1250T and Y1230D more strongly than wild type c-Met. The anti-proliferative activity of KRC-108 was measured by performing a cytotoxicity assay on a panel of cancer cell lines. The GI(50) values (i.e., 50% inhibition of cell growth) for KRC-108 ranged from 0.01 to 4.22 μM for these cancer cell lines. KRC-108 was also effective for the inhibition of tumo
价 格:¥电议型 号:T71382产 地:中国大陆
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T71381Exp6803;化合物 Exp6803Exp6803
Exp6803 is an Angiotensin II receptor antagonist.
价 格:¥电议型 号:T71381产 地:中国大陆
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T71380MLN-0415;化合物 MLN-0415MLN-0415
MLN-0415 is an IKK2 inhibitor which decreases NF-κB activation and down-regulates the expression of a number of inflammatory proteins.
价 格:¥电议型 号:T71380产 地:中国大陆
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T7138FB23-2;化合物FB23-2FB23-2
FB23-2 is a potent and selective mRNA N6-methyladenosine (m6A) demethylase FTO inhibitor(IC50 : 2.6 μM).
价 格:¥电议型 号:T7138产 地:中国大陆
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T71138LBinospirone;比螺酮MDL 73005EF;MDL 73005EF
Binospirone (MDL 73005EF) is a 5-HT1A receptor agonist with anxiolytic activity used in the study of glaucoma and movement disorders associated with neurologic dysfunction.
价 格:¥电议型 号:T71138L产 地:中国大陆
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T71138Binospirone mesylate;化合物 Binospirone mesylateBinospirone mesylate
Binospirone mesylate is a putative 5-HT(1A) receptor antagonist.
价 格:¥电议型 号:T71138产 地:中国大陆
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T71006BI-1388;化合物 BI-1388BI-1388
BI-1388 is a highly potent inhibitor of HCV NS3 protease activity, inhibiting viral replication for various HCV genotypes and for resistant mutants D168V and R155K.
价 格:¥电议型 号:T71006产 地:中国大陆
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T7021ZM241385;化合物ZM241385ZM241385
ZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.
价 格:¥电议型 号:T7021产 地:中国大陆
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T70138AZ0108;化合物 AZ0108AZ0108
AZ0108 is an orally bioavailable, potent PARP1,2,6 inhibitor that potently inhibits centrosome clustering and is suitable for in vivo efficacy and tolerability studies. AZ0108 has been utilized as in vitro tools and in vivo probes to investigate the biological consequences of inhibiting centrosome clustering through PARP enzymes. AZ0108 is more selective in its enzyme inhibition profile and effects on cellular pathways and phenotypes. Specifically, AZ0108 inhibits PARPs 1, 2, and 6 with approxi
价 格:¥电议型 号:T70138产 地:中国大陆
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T69138GW-406381X;化合物 GW-406381XGW-406381X
GW-406381X is a cyclooxygenase-2 (COX2) inhibitor.
价 格:¥电议型 号:T69138产 地:中国大陆
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T68281AZD-1386;化合物 AZD-1386AZD-1386
AZD1386 is an orally available antagonist of the transient receptor potential channel TRPV1. Note: Structure of this product was from NIH/NCATS web page: https://drugs.ncats.io/drug/210323T9CP and drugbank web page: https://go.drugbank.com/drugs/DB15333.
价 格:¥电议型 号:T68281产 地:中国大陆
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T68271AZD1386;化合物 AZD1386AZD1386
AZD1386 is a TRPV1 antagonist. AZD1386 acts as a competitive antagonist at the channel´s capsaicin binding site.
价 格:¥电议型 号:T68271产 地:中国大陆