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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T24798 | SK-7041 | SK 7041 | |
SK-7041 is an effective HDAC inhibitor that acts by preferentially inhibiting class I HDAC1 and HDAC2. | |||
T24797 | SK609 HCl | SK-609 HCl,SK609 hydrochloride,SK 609 HCl,SK 609 hydrochloride,SK-609 hydrochloride | |
SK609 HCl is a selective dopamine D3 receptor agonist. It also has atypical signaling properties. | |||
T34650 | SK&F 107461 | SK&F107461,SK&F-107461 | |
F 107461 is a hydroxyethylene dipeptide isostere. | |||
T26191 | SK&F 104976 | SK&F104976,Skf104976,Skf 104976,SK&F-104976,Skf-104976 | |
SK&F 104976 is a 32-carboxylic acid derivative of lanosterol. It was found to be a potent lanosterol 14 alpha-demethylase (14 alpha DM) inhibitor. | |||
T7524 | Metiamide | SK&F 92058 | Histamine Receptor |
Metiamide (SK&F 92058) is a histamine H2-receptor antagonist . | |||
T7133 | Anagliptin | SK-0403 | Proteasome , DPP-4 |
Anagliptin (SK-0403) is a potent Inhibitor of DPP-4(IC50 of 3.8 nM), for the treatment of type 2 diabetes mellitus. | |||
T34651 | SK&F 108361 | Skf-108361,SK&F-108361,Skf 108361,SK&F108361,Skf108361 | |
SK&F 108361 is a symmetric diol that binds HIV-1 protease symmetrically. | |||
TQ0126 | Mirodenafil dihydrochloride | SK-3530 dihydrochloride | PDE |
Mirodenafil dihydrochloride is a PDE-5 inhibitor developed for the treatment of erectile dysfunction. | |||
T69596 | SK-575 | ||
SK-575 is a Highly Potent and Efficacious Proteolysis-Targeting Chimera Degrader of PARP1 for Treating Cancers. SK-575 potently inhibits the growth of cancer cells bearing BRCA1/2 mutations and induces potent and specifi... | |||
T34652 | SK&F 39728-A | SK&F39728-A,SK&F 1-39728,SK&F-39728-A,Skf 39728-A | |
SK&F 39728-A is a bioactive chemical. | |||
T28787 | SK&F-95601 | SK&F 95601,SKF95601,SKF 95601,SKF-95601 | |
F-95601 is a proton pump inhibitor. | |||
T26190 | SK&F 106760 | SK&,F-106760,SKF 106760,SKF-106760,F106760,SKF106760,F 106760 | |
SKF 106760 is used as a glycoprotein IIb/IIIa antagonist. | |||
T28788 | SK-216 | SK216.Plasminogen activator inhibitor-1 (PAI-1) inhibitor | |
SK-216 is a specific PAI-1 inhibitor. SK-216 reduced the extent of angiogenesis in the tumors and inhibited VEGF-induced migration and tube formation by human umbilical vein endothelial cells in vitro. SK-216 reduced the... | |||
T29067 | Upacicalcet | PLS-240,SK-1403,AJT-240 | Calcium Channel |
Upacicalcet (AJT-240) is an intraventricular calcium mimetic, a SHPT available for human hemodialysis, that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on parathyroid cell membrane calcium-s... | |||
T20641 | Propagermanium | Dipropanoic acid germanium sequioxide,SK-818,Ge 132,Ge132,SK 818,Ge-132 | Others |
Propagermanium (Ge132), an organometallic compound of germanium, has been used as a therapeutic agent against chronic hepatitis B in Japan. | |||
T26644 | Apomine | SK&F-99085,APB-231-A2,APB-231-A-2,SR-9223i,SK&F-99085,SR-45023A | HMG-CoA Reductase |
Apomine (SR-9223i), an inhibitor of HMG-CoA-reductase, promotes apoptosis of myeloma cells in vitro and has been implicated in the regulation of myeloma in vivo. Apomine accelerates the degradation of 3-hydroxy-3-methylg... | |||
T24795 | SK&F 103784 | Skf 103784,Skf-103784,Skf103784 | |
SK&F 103784 is a vasopressin antagonist. | |||
T24796 | SK&F 107260 | Skf107260,Skf-107260,Skf 107260 | |
SK&F 107260 is an RGD-containing peptide. It is a potent GP IIb/IIIa antagonist and a vitronectin antagonist. | |||
T2218 | 8-Azaguanine | Azaguanine-8,SK 1150,NSC-749,SF-337 | Nucleoside Antimetabolite/Analog , Others , Endogenous Metabolite |
8-Azaguanine (SK 1150) is a purine analogue with potential antineoplastic activity. | |||
T70283 | SK 946 | ||
SK 946 is a cognition activator. |