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20

Compounds

Cat No. Product Name Synonyms Targets
T35862 Cucurbit[8]uril Others
Cucurbit[8]uril is a highly effective and safe supramolecular compound that promotes protein heterodimerization. It selectively induces the heterodimerization of methylviologen and naphthalene functionalized proteins, de...
T21246 Metsulfuron-methyl Others
Metsulfuron-methyl is a systemic selective wheat field high-efficiency sulfonylurea herbicide, which mainly controls most broadleaf weeds and grass weeds in wheat fields.
T7413 JNJ-5207852 Histamine Receptor
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
T9193 ACH-000143 Melatonin Receptor , MT Receptor
ACH-000143 have been identified as a novel agonist of the melatonin receptors MT1 and MT2.
T8646 URB937 FAAH
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
T13950 UC-514321 Apoptosis , STAT
UC-514321 directly targets STAT3/5 and represses TET1 expression. UC-514321 has the potential to treat acute myeloid leukemia (AML) both in vitro and in vivo, with low toxicity.
T9050 AG-270 Others , Methionine Adenosyltransferase (MAT)
AG-270 is an allosteric and orally active inhibitor of MAT2A.
T8418 DCLK1-IN-1 Others
DCLK1-IN-1 is a selective and in vivo-compatible chemical probe of the DCLK1 kinase domain .
T7057 Methylstat Histone Demethylase , Others
Methylstat is a methyl ester prodrug of a Jumonji C domain-containing histone demethylase (JMJD) inhibitor that has favorable cell permeability. The free acid of methylstat inhibits JMJD2A, JMJD2C, JMJD2E, PHF8, and JMJD...
T13974 ZL0580 Epigenetic Reader Domain , HIV Protease
ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
T2086 ELN-441958 ELN 441958 Bradykinin Receptor
ELN-441958 is a potent, neutral antagonist of B1 receptor, inhibits the binding of the B1 agonist ligand [3H]DAKD to IMR-90 cells with Ki of 0.26 nM. ELN-441958(ELN 441958) is highly selective for B1 over B2 receptors.
T5S0246 Pseudoprotodioscin Others , Fatty Acid Synthase
1. Pseudoprotodioscin has moderate cytotoxicity.
T10565 BMS-1001 hydrochloride PD-1/PD-L1
BMS-1001 hydrochloride is an orally active inhibitor of human PD-1/PD-L1 immune checkpoint with low-toxicity in cells.BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activat...
T9575 MRTX9768 Histone Methyltransferase
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
T7860 SM-324405 SM 324405 TLR
SM-324405 is an agonist of TLR7.
T1115 Doxylamine succinate Decapryn Histamine Receptor
Doxylamine Succinate is a pyridine derivate histamine H1 antagonist with pronounced sedative properties. Doxylamine succinate (Decapryn) competitively blocks the histamine H1 receptor and limits the typical allergic and ...
T9812 Tubulin inhibitor 24 Microtubule Associated
Tubulin inhibitor 24 is a potent inhibitor that can inhibit tubulin polymerization.
T4325 COTI-2 COTI 2,COTI2 Apoptosis , p53
COTI-2, an orally available thiosemicarbazone, is an activator of mutant forms of the p53 protein with potential antineoplastic activity.
T33639 Neotame NC 00723,HSDB 7965,NC-00723,NC00723 Others
Neotame (HSDB 7965) is a white-colored, dipeptide methyl ester, which is found to be a highly potent and non-nutritive sweetener or flavour enhancer and hence finds applications in a variety of foods.
T19031 NBD-F 4-Fluoro-7-nitrobenzofurazan Others
NBD-F (4-Fluoro-7-nitrobenzofurazan) is a fluorescent derivatization compound for amino acid analysis.
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