zineb

Zineb is an agricultural fungicide of the dithiocarbamate class. Zineb did not change the activity of any of the superoxide dismutases. The activity of catalase was reduced only by Zineb.

Zineb (Standard) is the standard substance of Zineb, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Zineb is an agricultural fungicide of the dithiocarbamate class. Zineb did not change the activity of any of the superoxide dismutases. The activity of catalase was reduced only by Zineb.

1-Piperazinebutanenitrile, 4-(3-chlorophenyl)- ,with CAS No. 118943-71-8, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1-Piperazinebutanenitrile, 4-(3-chlorophenyl)- provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

N'-Phenacylpiperazinebritanin is a useful organic compound for research related to life sciences and the catalog number is T131471.

PIPES (1,4-Piperazinediethanesulfonic acid) is an essential component of buffering agents used in biochemical applications, commonly referred to as PIPES buffer.

Methylbenactyzium Bromide (Semulgin) is an anticonvulsant that is the active metabolite of trimethadione.

Primordazine B is a small molecule that selectively ablates Primordial Germ Cells (PGCs). It functions by specifically inhibiting a process known as Poly(A)-tail Independent Non-canonical Translation (PAINT), without interfering with typical Poly(A) tail-dependent translation (PAT). Primordazine B serves as a valuable tool for investigating translational control mechanisms in specific physiological or pathological contexts, such as gene expression regulation during cell dormancy, viral infection, or stress conditions.

BMY-14802 (alpha-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazine butanol) is a selective and orally active sigma-1 antagonist with an IC50 of 112 nM.

Eleutherazine B is a useful organic compound for research related to life sciences. The catalog number is T126281 and the CAS number is 1175697-97-8.

Lenalidomide-C13-piperazine-Boc is a conjugate of an E3 ligase ligand and linker used in synthesizing the PROTAC degrader NC-R17.

Thalidomide-piperidine-C2-piperazine-Boc is an E3 Ligase Ligand-linker conjugate comprising a cereblon ligand based on Thalidomide and a linker. This compound is utilized in the synthesis of PROTAC.

Azido-PEG4-formylhydrazine-Boc is a PROTAC linker within the PEG category, suitable for PROTAC molecule synthesis. This compound serves as a click chemistry reagent, featuring an azide group that can participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAC) with alkyne-containing molecules. Additionally, it can undergo strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules bearing DBCO or BCN groups.

(S,R,S)-AHPC-CO-CH2-piperazine-C3-piperazine-Boc is a conjugate of an E3 ligase ligand and a linker (E3LigaseLigand-Linker Conjugates), consisting of (S,R,S)-AHPC and the appropriate linker. The (S,R,S)-AHPC moiety is a von Hippel-Lindau (VHL) ligand based on VH032, allowing the recruitment of VHL proteins. This compound can serve as a crucial intermediate for synthesizing complete PROTACs molecules.

(R)-Indeloxazine benzenesulfonate (AS1069562) is an orally active inhibitor of serotonin (5-HT) and norepinephrine (NE) reuptake, with IC50 values of 0.35 μM and 3.3 μM, respectively. It exhibits analgesic activity and can enhance neurological function by improving neurotrophic support.

Br-CO-piperazine-Boc is a PROTAC linker utilized in the synthesis of PROTAC molecules.

Desamino lenalidomide-piperazine besylate is an E3 ligase ligand-linker conjugate, which consists of a CRBN-based ligand and a linker, and is utilized in the synthesis of PROTACs.

Dihydrouracil-Ph-piperazine-Boc is an E3 ligase ligand-linker conjugate that includes a CRBN-based ligand and linker, suitable for PROTAC synthesis.

Pomalidomide-C2-piperazine-Boc is an E3 ligase ligand-linker conjugate, utilized in the synthesis of PROTACs, such as [PROTACBET Degrader-15].

1. Huperzine-B is a efficient inhibitor of human brain AChE. 2. Huperzine-B can enhance ognitive and protect neuro, may be potentially new drug candidates for Alzheimer's disease therapy.

Mesoridazine Besylate (Serentil) is a piperidine neuroleptic drug belonging to the class of drugs called phenothiazines, used in the treatment of schizophrenia. It is a metabolite of thioridazine.

Prolyldiketopiperazine B is a proline-based diketopiperazine.

Propyromazine bromide is an aticholinergic.

Tetrazine-biotin is a cleavable linker vital in ADC synthesis. Tetrazine-biotin joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

Thalidomide-piperazine-Boc, an intermediate used in the synthesis of BCL6 PROTAC, targets the B-cell lymphoma 6 protein.