20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T16834 | S26131 | N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide | MT Receptor |
S26131 (N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide) behaves as an antagonist on MT1 and MT2 receptors with Ki of 0.5 and 112 nM respectively. | |||
T32108 | HXJ42 | HXJ-42,HXJ 42 | Others |
HXJ42 is a PP1 analog that selectively and effectively acts on wild-type ZAP-70 (AS). | |||
T17266 | Xipamide | Diurexan,Aquaphor | Others |
Xipamide (Diurexan) is a sulfonamide-based diuretic with antihypertensive properties. Xipamide selectively inhibits anion exchanger. | |||
T8361 | Tetraethylammonium bromide | TEAB,TEA bromide | Potassium Channel |
Tetraethylammonium bromide (TEA bromide) can selectively block potassium channels. | |||
T77628 | Bisindolylmaleimide III | PKC | |
Bisindolylmaleimide III is a potent and selective inhibitor of protein kinase C (PKC).Bisindolylmaleimide III selectively interacts with PKCα or ribosomal S6 protein kinase 1 upon activation of these kinases. | |||
T8819 | SU-9516 | CDK | |
SU9516 is a selectively potent ATP-competitive inhibitor of CDKs. | |||
T7830 | Windorphen | Wnt/beta-catenin | |
Windorphen is a Wnt inhibitor that selectively abrogates the Wnt signaling. | |||
T9604 | Beta-Estradiol 17-hemisuccinate | Estrogen Receptor/ERR | |
beta-Estradiol 17-hemisuccinate selectively stains estrogen receptor (ER)-rich cells. | |||
T5536 | SJA710-6 | Others | |
SJA710-6 is able to selectively differentiate MSCs toward hepatocyte-like cells. | |||
T11533 | Z-HA155 | CS-963 | PDE |
Z-HA155 (CS-963) selectively and potently inhibits autotaxin with an IC50 of 5.7 nM. | |||
T6418 | BMS-378806 | BMS378806,BMS-806 | gp120/CD4 , HIV Protease |
BMS-378806 (BMS-806) selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus. | |||
T19319 | Ethyl docosa-4,7,10,13,16,19-hexaenoate | Others | |
Ethyl cis-4,7,10,13,16,19-Docosahexaenoate, the ethyl ester of Docosahexaenoate (DHA), is selectively enriched in the ethyl ester fraction through the alcoholysis process involving fatty acid ethyl esters from tuna oil a... | |||
T7008 | Vacquinol-1 | Vacquinol 1 | JNK |
Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death. | |||
T15769 | LMT-28 | IL Receptor | |
LMT-28 is an inhibitor of IL-6 and selectively inhibits IL-6-induced phosphorylation of gp130, STAT3, and JAK2. | |||
T37562 | C16 Ceramide | N-acylsphingosine,C16 Ceramide (d18:1/16:0),Palmitoyl Ceramide,N-Palmitoylsphingosine | p53 |
C16 Ceramide (Palmitoyl Ceramide) is a naturally occurring small molecule that activates p53 by directly and selectively binding to it. | |||
T24542 | NP-313 | NP 313,NSC 4264,NSC-4264,NSC4264 | |
NP-313 (NSC-4264) is a potent antithrombotic agent that inhibits platelet aggregation and activation by inhibiting thromboxane A 2 synthesis and selectively inhibiting SOCC-mediated Ca2+ efflux. | |||
T8745 | PROTAC BRAF-V600E degrader-1 | Compound 23 | Raf |
PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF. | |||
TP1015 | NFAT Inhibitor | VIVIT peptide | Others |
NFAT Inhibitor (VIVIT peptide) is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT. | |||
T28895 | T-0509 | T 0509,T0509 | Adrenergic Receptor |
T-0509 is a selective beta 1 receptor agonist that increases inotropy in canine ventricular muscle and selectively down-regulates rat cardiac beta 1-adrenoceptors. | |||
T6801 | CeMMEC13 | Carboxypeptidase , DNA/RNA Synthesis | |
CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 μM). |