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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12186 | Navitoclax-piperazine | ABT-263-piperazine | BCL , Ligands for Target Protein for PROTAC |
Navitoclax-piperazine (ABT-263-piperazine) is an inhibitor of B-cell lymphoma extra large (BCL-XL). | |||
T21569 | 1-(1-Naphthyl) piperazine hydrochloride | 1-naphthalen-1-ylpiperazine hydrochloride,1-(Naphthalen-1-yl)piperazine hydrochloride | Others |
1-(1-Naphthyl) piperazine hydrochloride (1-naphthalen-1-ylpiperazine hydrochloride) is a serotonergic ligand which could bind nonselectively with multiple serotonin (5-HT) receptors. | |||
T8582 | 1-[(5-methylisoxazol-3-yl)methyl]piperazine | Piperazine, 1-[(5-methyl-3-isoxazolyl)methyl]- (9CI) | P2Y Receptor |
1-[(5-methylisoxazol-3-yl)methyl]piperazine (Piperazine, 1-[(5-methyl-3-isoxazolyl)methyl]- (9CI)) is a P2Y12 inhibitor. | |||
T7146 | Piperazine adipate | Parasite | |
Piperazine adipate is a potent broad spectrum anthelmintic. | |||
T50020 | 1-(1-phenyltetrazol-5-yl)piperazine;hydrochloride | 1-(1-phenyl-1H-1,2,3,4-tetrazol-5-yl)piperazine hydrochloride | Others |
1-(1-phenyltetrazol-5-yl)piperazine;hydrochloride (1-(1-phenyl-1H-1,2,3,4-tetrazol-5-yl)piperazine hydrochloride) is a chemical derivative of piperazine that has been used as a starting material for the synthesis of othe... | |||
T16540 | Piperazine Erastin | Ferroptosis | |
Piperazine erastin is an analog of erastin. It causes an iron-dependent form of non-apoptotic cell death termed ferroptosis. | |||
T16539 | Piperazine citrate | GABA Receptor | |
Piperazine citrate, an organic compound, consists of a six-membered ring, containing two nitrogen atoms at opposite positions in the ring. It used as an Anthelmintic. | |||
T5105 | 1-(2-Pyridyl)piperazine | NSC13778 | Adrenergic Receptor |
1-(2-Pyridyl)piperazine (NSC-13778) is a selective α2-adrenoceptor antagonists. 1-(2-Pyridyl)piperazine shows sympatholytic activity. 1-(2-Pyridyl)piperazine is also a metabolite of Azaperone. | |||
T50018 | 1-(3-chloropyridin-2-yl)piperazine dihydrochloride | Others | |
1-(3-chloropyridin-2-yl)piperazine dihydrochloride is a piperazine analog often used as a reagent in organic synthesis, as a ligand in coordination chemistry, and as a drug in pharmaceuticals. It is an inhibitor of DPP4,... | |||
T0615 | 1-(3-Chlorophenyl)piperazine hydrochloride | M-CPP hydrochloride | Others |
1-(3-Chlorophenyl)piperazine hydrochloride (M-CPP hydrochloride) is used for the synthesis of trazodone, Etoperidone, Nefazodone, etc. | |||
T40034 | GNF-8625 monopyridin-N-piperazine hydrochloride | Trk receptor | |
GNF-8625 monopyridin-N-piperazine hydrochloride is a protomyosin receptor kinase (TRK) inhibitor. | |||
T0345 | Estropipate | Piperazine estrone sulfate,Pipestrone,Estrone sulfate piperazine salt | Estrogen Receptor/ERR , Estrogen/progestogen Receptor |
Estropipate (Piperazine estrone sulfate) is a natural estrogenic substance composed of estrone sulfate and piperazine. | |||
T60231 | N-[2-nitro-4-(trifluoromethyl)phenyl]piperazine | Others | |
N-[2-nitro-4-(trifluoromethyl)phenyl]piperazine is a biologically active compound belonging to the piperazine group. It is an important synthetic intermediate used in the preparation of a wide range of drugs, agrochemica... | |||
T9876 | Piperazine, 1-(4-fluorophenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]- | Others | |
Piperazine,1-(4-fluorophenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]- is a piperazine derivative with anti-SARS-CoV-2 activity. | |||
T40111L | BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride | PD-1/PD-L1 | |
BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride is a resorcinol di-Ph ether scaffold-based programmed cell death-1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitor that inhibits the PD-1/PD-L1 interaction wi... | |||
T50034 | 1-{1H-pyrrolo[2,3-d]pyrimidin-4-yl}piperazine dihydrochloride | Others | |
1-{1H-pyrrolo[2,3-d]pyrimidin-4-yl}piperazine dihydrochloride (1-PPZ-DHC) is a compound used as a molecular structural unit. It is an analog of the natural product piperazine and has a wide range of biological activities... | |||
T39895 | Thalidomide-Piperazine-PEG3-NH2 | Thalidomide-Piperazine-PEG3-NH2 | |
Thalidomide-Piperazine-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that combines the Thalidomide-based cereblon ligand with a linker commonly used in PROTAC technology, serving as an E3 ligase recruiter. | |||
T39893 | Thalidomide-Piperazine-PEG2-NH2 | Thalidomide-Piperazine-PEG2-NH2 | |
Thalidomide-Piperazine-PEG2-NH2 is a synthetic E3 ligase ligand-linker conjugate that combines the cereblon ligand derived from Thalidomide with a linker commonly utilized in PROTAC technology. | |||
T28882 | Sultosilic acid, piperazine salt | A-585,Mimedran,piperazine-sultosylate,A585,A 585 | |
Sultosilic acid piperazine salt is a drug with lowering lipid activity. It causes significant shortening of the euglobulin lysis time and a significant diminution of platelet adhesiveness, as well as statistically signif... | |||
T67739 | BMY-14802 | alpha-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazine butanol | Sigma receptor |
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. |