20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T15247 | ESI-05 | NSC 116966 | cAMP |
ESI-05 (NSC-116966) is a specific EPAC2 (exchange protein directly activated by cAMP 2) antagonist (IC50: 0.4 μM). ESI-05 inhibits cAMP-mediated activation of EPAC2, as well as EAPC2, mediated Rap1 activation. | |||
T0373 | Erlotinib | OSI-744,NSC 718781,CP358774,R1415 | EGFR , Autophagy |
Erlotinib (NSC-718781) is an EGFR inhibitor (IC50: 2 nM). It is used for the treatment of non-small cell lung cancer. | |||
T23401 | Strontium chloride | Others , CaSR | |
Strontium chloride is an agonist of Calcium sensing receptor (CaSR) and directly affects C-type nerve fibers. | |||
T9734 | InhA-IN-2 | CDK | |
InhA-IN-2 directly inhibits InhA and does not require activation by the catalase peroxidase KatG. | |||
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. | |||
TP2307 | Pinealon Acetate | Others | |
Pinealon Acetategland has antioxidant activity and can directly interact with the cell genome. | |||
T24729 | Roseoflavin | Antibacterial | |
Roseoflavin, a chemical analog of FMN and riboflavin that has antimicrobial activity, can directly bind to FMN riboswitch aptamers and downregulate the expression of an FMN riboswitch-lacZ reporter gene in B. subtilis. | |||
T26408 | A 21960 | Ethyl 2-chloroacetoacetate,A21960,A-21960 | |
A 21960 (Ethyl 2-chloroacetoacetate) inhibits synapse formation between resolvase and two directly repeated res sites, blocks site-specific recombination reactions, and can be used to study bacterial infections. | |||
T1494 | Alarelin Acetate | Alarelin | GNRH Receptor |
Alarelin Acetate is a synthetic GnRH agonist which can directly inhibit proliferation and DNA synthesis of rat GSMC through GnRH receptors. | |||
T2450 | SANT-1 | SANT 1 | Hedgehog/Smoothened , Smo |
SANT-1 directly binds to Smoothened (Smo) receptor (Kd: 1.2 nM) and inhibits Smo agonist effects (IC50: 20 nM). | |||
T12478L | Pinacidil | S 1230,P 1134,S-1230,P-1134,P1134 | Potassium Channel |
Pinacidil (P 1134) is a guanidine that opens potassium channels and directly dilates peripheral blood vessels in small arteries, lowering blood pressure and peripheral resistance and producing fluid retention. | |||
T11986L | Mebeverine acid hydrochloride | ||
Mebeverine acid hydrochloride is an effective, oral compound to act directly on the smooth muscle of the gastrointestinal tract to relieve spasticity symptoms. | |||
T12616L | CE3F4 | cAMP | |
CE3F4 is a selective antagonist of exchange protein directly activated by cAMP (Epac1; IC50s of 10.7 μM and 66 μM for Epac1 and Epac2(B), respectively). | |||
T38563 | Raptinal | Caspase | |
Raptinal activates caspase-3 directly and initiates intrinsic caspase-dependent apoptosis pathway in multiple cell lines. | |||
T60051 | VPC-18005 | Others | |
VPC-18005 is a luciferase inhibitor. VPC-18005 inhibits ERG-induced transcription and interacts directly with the ERG-ETS domain thereby disrupting the ERG binding to DNA. | |||
T11666 | IPR-803 | Serine/threonin kinase | |
IPR-803 is an effective inhibitor of the uPAR·uPA protein-protein interaction (PPI) with anti-tumor activity. IPR-803 binds directly to uPAR with a Ki of 0.2 μM. | |||
T1810 | Purmorphamine | Shh Signaling Antagonist VI | Hedgehog/Smoothened , Smo , Autophagy |
Purmorphamine (Shh Signaling Antagonist VI), which directly binds and activates Smoothened, blocks BODIPY-cyclopamine binding to Smo. It also is an inducer of osteoblast differentiation. | |||
T14848 | C 87 | Others , TNF | |
C 87 is a small-molecule TNF-α inhibitor. C 87 directly binds to TNFα, potently inhibits TNF-α-induced cytotoxicity (IC50 = 8.73 μM), and effectively blocks TNF-α-triggered signaling activities. | |||
T6762 | AS1842856 | Autophagy , FOXO1 | |
AS1842856, a cell-permeable inhibitor, can block the transcription activity of Foxo1 (IC50: 33 nM). It can directly bind to the active Foxo1, but not the Ser256-phosphorylated form. | |||
T8874 | FB23 | Others | |
FB23 directly binds to FTO and selectively inhibits FTO's m6A demethylase activity. (FTO, an mRNA N6-methyladenosine (m6A) demethylase, was reported to promote leukemogenesis.) |