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Search Results for " control compound "

20

Compounds

Cat No. Product Name Synonyms Targets
T15441 GSK8573 Epigenetic Reader Domain
GSK8573 is an inactive control compound for GSK2801. GSK8573 has binding activity to BRD9 (Kd of 1.04 μM).
T10608 BRD5648 (R)-BRD0705 GSK-3
BRD5648 ((R)-BRD0705) is an inactive (R)-enantiomer of BRD0705. BRD0705 is a GSK3α inhibitor (IC50: 66 nM; Kd: 4.8 μM) and can be used in acute myeloid leukemia (AML) studies.
T60023 CL-278474 Others
CL-278474 (compound I-79) is a potent inhibitor of β-N-acetylhexosaminidase OfHex1. CL-278474 can be used in control of insect.
T23478 Trometamol hydrochloride TRIS hydrochloride Others
Trometamol hydrochloride (TRIS hydrochloride) (Tromethamine hydrochloride) is a biologically inert amino alcohol with low toxicity. Trometamol hydrochloride buffers carbon dioxide and acids in vitro and in vivo. Trometam...
T0898 Chloroxylenol 5-dimethylphenol,4-Chloro-3,4-Chloro-3,5-dimethylphenol,PCMX Influenza Virus , Antibacterial , Antibiotic
Chloroxylenol (PCMX) (4-chloro-3, 5-dimethylphenol), a broad spectrum antimicrobial chemical compound, is used to control virus, bacteria, fungi, and algae. It is used in households and hospitals for sanitation and disin...
T2035 WHI-P258 EGFR , JAK , JNK
WHI-P258 is a dimethoxyquinazoline inhibitor of JAK3. This compound binds JAK3 weakly and may be used as a JAK-binding negative control in the development of new therapeutics.
T13877 (S,S,S)-AHPC hydrochloride (S,S,S)-VH032-NH2 hydrochloride Ligand for E3 Ligase
(S,S,S)-AHPC hydrochloride ((S,S,S)-VH032-NH2 hydrochloride) is a VHL amino building block, is a ligand used as a negative control for (S,R,S)-AHPC. It is the VH032-based VHL ligand used in the recruitment of the VHL pro...
TP2203 Bax inhibitor peptide, negative control Others
The compound is a negative control peptide for the Bax inhibitor peptides V5 and P5.
T31831 Fluvalinate Kartan,Fluvalinate II,Fluvalinate I,Mavrik,Klartan,Apistan
Fluvalinate is a synthetic chemical compound and can be commonly used to control varroa mites in honey bee colonies.
T39239 TRC-766
TRC-766, a negative control of RTC-5 (TRC-382), is a compound that exhibits protein phosphatase 2A (PP2A) binding properties while lacking phosphatase activation capabilities.
T40822 TRPA1 Antagonist 3 TRPA1 Antagonist 3
TRPA1 Antagonist 3 is a compound with photoswitchable properties that acts as an agonist on the TRPA1 channel, providing the ability for optical control.
T29063 UNC-4219 TFA UNC4219,UNC-4219,UNC 4219
UNC4219 is a negative control compound for UNC3866, a potent antagonist of the methyllysine (Kme) reading function of the Polycomb CBX and CDY families of chromodomains.
T70662 UCSF924NC
UCSF924NC is the recommended negative control compound for the high-affinity dopamine D4 receptor (DRD4) partial agonist UCSF924. UCSF924NC exhibits a 1/2500-fold reduced D4 affinity when compared with that of UCSF924.
T36505 Sulpho NONOate
Sulpho NONOate produces nitrous oxide but no NO at physiological pH. Therefore, this compound may be used as a negative control in experiments using other NO donors of the NONOate class.
T38743 Scrambled TRAP Fragment
Scrambled TRAP Fragment is a variant of the TRAP Fragment compound, characterized by its random amino acid sequence. It is typically employed as a negative control due to its similarity in composition to the active fragm...
T39750 CMP98
CMP98, a proteolysis targeting chimera (PROTAC), exhibits a lack of VHL degradation efficacy. It can function as a negative control compound in comparison to CM11. CMP98 comprises two von Hippel-Lindau ligands operating ...
T36240 AP219
AP39 is a compound used to increase the levels of hydrogen sulfide (H2S) within mitochondria. It consists of a mitochondria-targeting motif (triphenylphosphonium) coupled to an H2S-donating moiety (dithiolethione) by an ...
TN3626 Cerbinal Antifection
Cerbinal is a natural compound derived from the African herb Gerbera. It has insecticidal activity and is a potential new pest control agent.
T36305 FMF-04-159-R
Potent inhibitor of CDK16 and CDK14 (IC50 values are 6 and 140 nM, respectively in kinase activity assay; IC50 = 563 nM for CDK14 in BRET assay). Also binds CDK2 (IC50 = 493 nM). Inhibition reversible upon compound wash-...
T69012 Cinnarizine clofibrate
Cinnarizine clofibrate is a calcium channel protein inhibitor as well as an antihistamine channel blocker. The compound is a drug derivative of piperazine. Cinnarizine is used for the control of vomiting due to motion si...
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